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Heat Stress Management via Nutritional Strategies for Broilers

Written By

Maleeka Nambapana and Dinesh Jayasena

Submitted: 06 June 2024 Reviewed: 06 June 2024 Published: 01 July 2024

DOI: 10.5772/intechopen.1005810

Modern Technology and Traditional Husbandry of Broiler Farming IntechOpen
Modern Technology and Traditional Husbandry of Broiler Farming Edited by Waleed Al-Marzooqi

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Modern Technology and Traditional Husbandry of Broiler Farming [Working Title]

Dr. Waleed Al-Marzooqi

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Abstract

Over the last decades, the rate of broiler production has been increased to encounter the increase growing demand and to assure the food security among the human. Heat stress is kind of a leading concern in the broiler productiveness because it directly has effects on the profit of the industry. Poultry birds can standardize their body temperature with a much tapered range of environmental temperatures. High ambient temperature unpleasantly effect on the enactment of broiler birds rather than other livestock species. The unfavorable effects of increased heat include reduce growth performances, deprived meat quality, impairing metabolic activities, destructive morphology of gastrointestinal tract, wearying immune functions, prejudicing hematological parameters and endocrine systems, etc. Henceforth, observance in the opinion the present condition, it is essential to recognize the depth of the combative consequences of high environmental temperature on broilers and look advancing to diminish the influence wherever. Thus, introducing upgraded genes, modified housing condition, altering management practices, novel feeding techniques and nutrition management via changing compositions of the diet, acquaint with innovative feed additives are some preferences which can be adhered to. The emphasis of this article is to unfold the evidence on disparaging influences and open the eye of stake holders to take corrective measures while disseminating the findings of scholars.

Keywords

  • broilers
  • heat stress
  • performances
  • nutritional management
  • feeding strategies

1. Introduction

The intensive commercial production of poultry faces a myriad of challenges and stressors that impact the physiological well-being of the birds. These challenges include heat stress, high stocking densities, nutritional imbalances, and disease outbreaks. One major concern for broiler producers worldwide is the effect of high environmental temperatures on their birds. Broilers lack sweat glands and are fully covered in feathers, making it difficult for them to regulate their body temperature during hot weather conditions. The optimal temperature range for poultry, referred to as the comfort zone, typically falls between 16°C and 25°C [1]. Temperatures that exceed this range can result in heat stress. In tropical regions where temperatures fluctuate significantly throughout the year, poultry are particularly vulnerable to heat stress.

When chickens are exposed to heat stress, they employ various strategies to regulate their body temperature and maintain normal bodily functions. These include reducing feed intake; limiting physical activity such as walking and standing; and increasing resting time, drinking, and panting [2]. The continuous panting in response to heat stress (HS) can disrupt the blood pH balance, leading to respiratory alkalosis. This can impair the immune system’s function and disrupt hormonal activities in the body [3].

Heat stress also has negative effects on production performance in broilers. It is associated with poor fertility, dehydration, low survival rates, and increased morbidity and mortality rates. Additionally, it alters meat quality by increasing adiposity (fat deposition) while reducing skeletal muscle mass [4, 5, 6].

Collectively, these impacts of HS result in significant economic loss for the poultry industry. Indeed, addressing heat stress in poultry flocks is crucial during hot weather periods. Improving the housing environment is one approach, and nutritional manipulation can also play a significant role in mitigating the negative effects of heat stress on poultry birds. In this chapter, we will discuss the impact of heat on broiler performances and explore various strategies to minimize heat stress. Additionally, we will delve into nutritional interventions that can help alleviate heat stress and examine both conventional and modern techniques of nutritional management, which can be employed in broiler farming to effectively combat the HS.

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2. The effect of heat on broiler production

The increasing global demand for animal protein, coupled with the rise in human population, has led to a significant growth in poultry production, particularly broiler production. This increase is necessary to meet the food and livelihood needs of consumers. In the recent decades, there has been a steady increase in the consumption of poultry meat worldwide.

According to the Food and Agriculture Organization (FAO), global poultry meat production reached an estimated 133 million tons in 2020, accounting for 40% of total meat production (excluding fish). Poultry farming is considered to be one of the most efficient animal protein production systems with a relatively small carbon footprint per unit of product.

Poultry industry plays a prominent role in agricultural industries across many parts of the world. It is increasingly seen as a healthier alternative to red meat and other sources of protein. Chicken meat, in particular, has gained popularity due to its lower cost and high nutritive value. As demand continues to grow, there is a need for fast-growing broiler chickens that can meet market demands. Therefore, constant genetic improvement is being carried out in broilers to enhance their growth rate and improve the quantity and quality of chicken meat produced. This ensures that the industry can keep up with consumer demands while providing nutritious and affordable poultry products.

The modern hybrid poultry strains are growing faster than the old strains and their genotypes are advanced to have greater metabolic activity which causes them to become more delicate to thermal relevant ecological changes. Thus, the modern broiler chickens reach a marketable weight of 2 kg within 35 days due to their rapid growth rates with high production efficiency. However, ideal growth of the broiler bird can be reached by rearing them under thermoneutral zone of 18–24°C [7].

At present, global warming leads to increase in the environmental heat and is reasoned to make a huge stress on broiler farming and their production efficiency. Therefore, it is required to define the stress derived from the heat on broiler production and the effect of heat cope up with losing the efficiency of the broiler industry.

Heat stress means the inequality between the heat energy production in the animal and the heat energy that dissipates from the body of the animal to the environment. According to the strength of heat derived from the body and incorporation of humidity and thermal irradiation like environmental factors with age, thermoregulatory ability, and metabolic rate of animal, HS can be classified into three dimensions such as mild, moderate, and severe. According to Ref. [8], two concepts were revealed on HS such as exposure of high temperature for short period as acute heat and disclosure of increased temperature for prolonged period mentioned as chronic heat stress. Because of the absence of sweat glands and plumage coverage in poultry birds at high temperatures, broilers struggle to maintain their body temperature within the normal range and various stress reactions are elucidated to guarantee the body functions, which happen at an average rate. Due to the strain, feathering rate, nutrient availability, and the management system, the intensity of HS may vary in broiler industry.

In the case of broilers, numerous physiological responses can be identified in different systems such as neuroendocrine, immune, digestive, and circulatory. Further, HS affects feeding process, nutrition digestion on enzymatic activities, nutrition absorption via altering histology of absorptive surfaces, metabolic path ways, hematological parameters, etc. There are solemn negative effects which caused to physiological malfunctions of broilers while reducing the sustainable productivity with increased temperature on broiler production systems were recorded in tropical countries.

2.1 Symptoms of heat-stressed broiler birds

Raising wings away from body, gasping with open mouth, fatigued, deliberateness, weary eyes, high water intake, lying down without active movement, diminished appetite, descent body weight, augmented cannibalism are some of the investigated signs of HS in broiler birds [9, 10]. Further, Ref. [11] observed that broiler birds are trying to lose heat by panting with open mouth which helps to cool the surface of lungs while heat-stressed birds devote more time for drinking water rather than for feeding. In addition, researchers were revealed that increased glucocorticoids and catecholamine production, lower metabolism of thyroid hormones, reduced immune responses from weaken lymphoid organs, elevating lipid peroxidation while damaging the health of survival birds are identified internal signs of HS [12, 13, 14, 15].

2.2 Reactions of heat-stressed broilers

In high temperature when HS occurs, neurogenic system gets activated and accordingly blood pressure, muscle degeneration, nerve sensitivity, blood sugar level, and rate of respiration are increased as a first reaction. When the first reaction doesn’t work, the hypothalamic-pituitary-adrenal cortical system come into forefront and inducing of hypothalamus releases corticotrophin-releasing factors and raises the activity of pituitary gland which releases corticotropin hormone simultaneously [16]. The proliferation of adrenal cortical tissues start to release corticosteroids and Ref. [17] investigated that high level of blood corticosterone concentrations while Ref. [18] recorded the decreased level of thyroxine and adrenaline hormone levels in heat-stressed broilers.

2.3 Effect of heat stress on broiler production performances

Further researchers have investigated few of the detrimental effects such as low feed intake, decreased weight gain, reduction of meat quality, increased mortality rate, high morbidity, lower feed conversion efficiency, etc. from heat-stressed broiler birds [19, 20, 21, 22, 23, 24, 25]. In addition, Table 1 explains the effect of heat stress on different functions of broilers.

Heat stress conditionType of effect on broilersReference
32°CHigh metabolizable energy intake (20.3%)
Increased heat production (35.5%), lower energy retention (20.9%), decreased energy efficiency (32.4%)
[26]
34°C of temperature for 6 h daily from 22 to 35 daysLow feed intake (FI) around 8–9% and dropped down of body weight gain (BWG) by 17%[27]
32°C from 17th to 42nd of age5–10% higher intake of water[28]
34–36°C-chronic heat stressDecrease in breast muscle mass (31.53%) and thigh muscle (11.17%)[22]
(33°C for 9 h, 25°C for 15 h 1–42 days) cyclical HSReduced breast muscle weight by 16% (42)[29]
(32°C for 14 days)Increased intramuscular fat, raised activity of pyruvate kinase and lactate dehydrogenase in pectoral muscles[30]
32.2–37.8°CDeduction in feed intake of 9.9%/bird/day[31]
High mitochondrial ROS production[32]
Acute heat stressIncrement of oxidative stress, mitochondrial ROS generation in the skeletal muscle[33, 34]
Decreased growth rate and feed intake, and increasing morbidity[35]
35–45°CReduction of growth performance in poultry[36]
Increased concentration of uric acid[37]
34 ± 2°C for 8 h/day, 08:00–17:00 hReduction in serum, liver, and breast muscle Cr concentrations[38]
36 ± 2°CReduced dressing percentage, lower gaining of body weight, decreased protein digestibility, low feed intake, reduced relative weight of breast muscles, reduction in PCV, monocyte, basophil, total protein, albumin and glucose and increment of heterophil/lymphocyte ratio, cholesterol, AST[39]
33 ± 0.5°C for 3 hLow growth performance (average daily gain, average daily feed intake, and feed conversion ratio)[40]

Table 1.

Effect of heat stress on different functions of broilers.

Moreover numerous physiological turbulences such as hyperpnoea, electrolyte inequity, fast pulse rate, vascular dilatation, endocrine disarrays, irregularities in immune system, muscle shocks and faintness, and collapse occur in heat-stressed birds that prejudice the welfare and production efficiency were observed in heat-stressed broilers [41, 42].

Moreover the cyclic heat stress caused to reduced feed intake by 15% and constant heat effect further reduced feed intake by 25–45% due to the findings of Ref. [43]. Same authors confirmed that 1.5% decline in feed intake °C−1 in cyclic heat stress and 3.5% lessening in feed intake °C−1 in constant heat stress were recorded during their researches.

Consequently body weight gains of heat-stressed broilers were declined due to the effect of low feed intake, nutrient digestion and assimilation which could be ascribed to a decrease in intestinal weight, length, and altered villus structure in broiler chicken affected by HS. Further Ref. [44] suggested that inflection in nutrient transport genes can be affected by HS and caused to reduce the ability of nutrient assimilation process. Correspondingly dry matter digestibility of broilers in high temperature has decreased by 1.6–3.9% and lower crude protein or nitrogen digestibility were recorded due to the lower activity rates of digestive enzymes such as trypsin, chymotrypsin, lipase, amylase, and maltase [45, 46, 47, 48].

Besides the performance parameters Ref. [30] elaborated poor meat quality characters, depression of chemical composition of chicken meat, reduced carcass weight, reduced breast and thigh meat weight, low breast meat yield, increased shear force values, and high level of abdominal fat percentages were elucidated because of exposure of heat stress during rearing period [21, 22, 49, 50]. Moreover, declining pH, increased oxidation, high malonaldehyde concentration in liver and breast meat, incidence of pale, soft, exudative in broiler chicken were reported by Ref. [51].

Further, Ref. [52] was found that lower antioxidant defense ability, increased lipid peroxidation levels, reduction of protein synthesis while increase in catabolic rate of proteins, lower RNA concentration in pectoralis muscle tissue in chicks exposed to high temperature [44, 53].

2.4 Effect of heat stress on reproduction performances of broiler birds

Different studies were conducted to evaluate the influence of heat stress on reproductive activities of broiler birds and investigated that reducing luteinizing hormone (LH) levels and hypothalamic gonadotropin-releasing hormone-I (GnRH), decrease size of reproductive organs, delaying ovulation process, low quality of semen in broiler breeders [54, 55, 56, 57].

2.5 Effect of heat stress on immunological responses of broiler birds

Immune responses of heat-stressed broiler chicken were identified by several researches and revealed that reduced the size and weight of lymphoid organs, reduced intestinal barrier functions whereas disturbing the blood flow from the gastrointestinal tract (GIT) to the skin, consequently damages the mucosal tight junction barrier in the GIT and it caused to escalation the permeability to transmit luminal endotoxins to the birds’ body [58, 59]. Therefore the increment of penetration of pathogens such as Salmonella sp., Clostridium sp., and Escherichia coli reasoned to decline the immune performances like increase colonization of destructive bacteria, high invasion of inflammatory microorganisms in heat-stressed broiler birds [60].

Further Ref. [61] confirmed that the reduction of T and B lymphocytes production, lower phagocytic activity of blood leucocytes, decline of total antibodies, fall of IgM and IgG levels, drop down of white blood cells and activities of leukocytes in heat-stressed broilers. As to support the aforesaid statement, Ref. [62] investigated accent of the immune responses by central nervous system (CNS), damaged lymphoid tissues, suppressed humoral and cell mediated immunity, lower lymphocytes to heterophil ratio, reduction of phagocytic activity of macrophages, macrophage basal and oxidative burst were observed from heat-stressed broilers by Refs. [63, 64].

2.6 Effect of heat stress on morphology of intestinal tract of broiler chicken

High temperature effects negatively on morphology of absorptive surface area of small intestine in broiler chicken by reducing relative weight of jejunum, villus height, crypt depth, cell proliferation and appearing of heat shock proteins (HSP70) in liver, heart, duodenum, jejunum, ileum were detected by Refs. [45, 65, 66, 67, 68]. In addition, Ref. [67] corroborated that HS destructively effect on gut integrity composed of enterocytes and tight junctions of small intestine in broiler chicken.

2.7 Effect of heat stress on hematological parameters of broiler chicken

Alteration of multiple blood parameters of broiler chickens which are exposed to high temperature were reported by different authors such as increment of heterophil to lymphocyte (H:L) ratio, decline in thiobarbituric acid reactive substances, movement in blood minerals and glucose concentration, changes in serum concentrations of uric acid, aspartate aminotransferase (AST), creatine kinase, total protein, albumin, and globulin [69, 70, 71, 72]. Recently, Ref. [73] investigated that reduction in plasma CO2, HCO3, and potassium and an increase in pH caused respiratory alkalosis and increase of glucose levels once the broilers were opened to over 33°C temperature at 5 h/day. Further, aforesaid author confirmed that reduction of K and Na levels of plasma which caused to increase water consumption and reasoned to occur hemodilution and Ref. [74] elaborated all those negative effects may finally have influence on plasma hematocrit, uric acid, total protein, and globulin levels in heat-stressed broilers. Moreover, Japanese quails which exposed to high temperature had lower blood vitamin E level by 29% and ascorbic acid level by 40% elucidated by Ref. [75].

2.8 Effect of heat stress on endocrine system of broilers

Plasma triiodothyronine (T3), thyroxine (T4), and adrenaline levels were declined and high corticosterone levels of quail broilers and chicken broilers were reported by Ref. [4]. Further, Ref. [76] reported that stress indicators such as corticosterone, ceruloplasmin, and ovo transferrin were detected in heat-stressed broiler chicken.

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3. Different approaches can be used to diminish the effect of heat stress

Considering the destructive effects of high temperature and its influence on broiler industry, researchers and the stakeholders of the poultry industry advocated numerous findings which can be applied in the ongoing process of broiler husbandry. Extenuating the adversative effects caused by increased temperature in broiler birds entails holistic and multi-factorial processes. Different authors have focused on modified housing facilities [77], altering routine management practices, selection of heat tolerant broiler strains [78], novel feeding techniques and nutrition management [79, 80], etc.

3.1 Modification of poultry housing conditions

Open housed poultry cages are needed to be established toward the east to west directions with the roof angled at 45 degrees, some of modified farms have designed with sprinkle watering system to the rooves. Exhaust fans, cooling pads (wet pads), air conditioners, misting systems, and automated curtains were occupied with closed housed poultry cages which were designed with modern technology. In addition, altering the environmental conditions of poultry cages by increasing in air velocity to 2–2.5 ms−1 and introducing fresh air to the rate of 6–7 m3/kg of body weight/h in to the cages were suggested by Refs. [81, 82]. Moreover, introducing novel techniques such as use heat insulating and reflective materials for rooves, spray cold water to the roof, reducing the thickness of bedding materials less than 5 cm are some of the counteractive measures that can be implemented to mitigate the HS on broilers [83, 84, 85, 86].

3.2 Altering management practices

3.2.1 Expose to heat shock treatment

Refs. [87, 88] revealed that heat resistance and weight gain can be improved by exposing eggs to heat treatment at the pre stage of hatching (39.5°C/12 h/day, from days 7 to 16 of incubation) and after hatching of chicks (35–37.8°C, 24 h, on day 5 after hatching).

3.3 Selection of heat tolerant broiler strains

The introduction of heat tolerant indigenous broiler breeds/strains such as Naked neck (Na), Frizzle (F), and Dwarf (Dw) are commended by Ref. [89] and Naked neck breed having 40% lower feather coverage and increased immunity under high temperature conditions compared to normal broiler chicken as Ref. [90] elaborated.

Other than genetic selection multiple nutritional strategies have been suggested to alleviate destructive effects of HS in the poultry industry.

3.4 Alleviation of heat stress via feeding management

Ref. [91] suggested several management strategies relevant to feeding such as allocating different forms of feed and coarser diets, practice wet feeding, introduce free choice and diurnal feeding patterns can be implemented to alleviate the influence of high temperature for broiler birds.

3.4.1 Change the form of feed

Mash, crumble, and pellets are the three different forms of feed available for broiler birds and Ref. [91] reported that broilers rear in hot climate conditions, prefer to intake feed with larger particle size in which reduce the heat generation due to prolong feeding. Similarly Ref. [92] confirmed that broilers fed with pelleted diet in high temperature conditions showed an increment of feed intake, body weight gain, and crude protein digestibility by 10%, 8.3%, and 2.3%, respectively and increased energy utilization, lower relative weight of digestive tract which cause to reduce the maintenance energy requirement for intestinal tract, increment of villus length and villus to crypt depth ratio in the jejunum, improved carcass weight and yield were observed by Ref. [93].

Nonetheless, Ref. [94] analyzed the use of coarse particles (2280 μm) of corn increased panting compared to finer particles (605 μm) in broilers fed a mash diet under natural HS conditions.

3.4.2 Practice special feeding regime

Some of the authors have recommended to practice feeding 4–6 h prior to the reaching high temperature levels such as early morning and late evening or night feeding in order to reduce the heat load of broilers [82, 95].

3.4.3 Feeding time and space

Some of studies revealed that animals kept under fasting condition, produce low heat compared to the full fed animals and aforesaid authors suggest to have feed withdrawal during the high temperature conditions while allocating feed for the duration of low temperature conditions and they observed improvements in feed consumption among heat-stressed broilers [96, 97].

3.4.4 Feed restriction and feed withdrawal

Heat production has been reduced by 23% with having feed restriction from 44 to 48 weeks of broiler breeders and reduction of rectal temperature, mortality and feed conversion ratio, heterophil-to lymphocyte ratio while having 75–50% feed restriction compared to full fed broilers was reported by Refs. [96, 98]. Ref. [99] confirmed that he received the same results such as minimum negative effects of HS by applying feed restrictions and feed restriction at early stages caused to encourage heat tolerance at latter part of the growing period of broilers.

3.4.5 Practice dual feeding

Broiler birds affected with HS are directed to the two different consecutive diets such as protein and energy concentrated feeds for a specific period achieved lower body temperature, mortality and recommended to give protein concentrated diet during low temperature and energy rich diet at high temperature time [100]. In addition, the study conducted with high energy low protein diet and low energy with high protein diet proved same performances in heat-stressed broilers.

3.4.6 Facilitate for choice feeding

By allowing for choice feeding in HS broilers, some of authors investigated that those broilers had improved the heat tolerance and during the high temperatures broilers preferred to intake less protein and high energy content feed ingredients to reduce the heat production [101, 102].

3.4.7 Increase the access for wet feeding

Water is one of the most chief nutrients in broiler nutrition, and plays a vital role for thermoregulation under hot temperatures, and promoting wet feeding is an attempt to maximize water intake and utilization. Several studies have investigated that increased body weight gain, feed intake, dry matter intake, carcass weight, protein content in chicken, abdominal fat and lipid content, and low dry matter conversion efficiency can be achieved from HS broilers by mixing feed with water in 2:1 or 1.5:1 ratio [103, 104].

However, Ref. [93] observed wet feeding increased abdominal fat, abate breast HSP70 mRNA expression, breast creatine kinase protein level, low FCR and heterophil-to-lymphocyte ratio, and high passage rate of digesta in HS broilers [105].

3.5 Increase the availability of water

According to NRC [19], water intake of chicken escalations by about 7% for each 1°C increase above 21°C. Reduction of water intake directly related to lower the production because at high temperatures broilers consume more water than their diet. Temperature of water, type, shape and height of drinker and some authors investigated that intake of water reduces, when use nipple lines rather bell drinkers in high temperature [106]. Aforesaid authors reported that the height of drinker also affected to heat production in broilers due to stretching of neck muscles and broiler birds may get high opportunity to immerse their whole face in to water to relief heat stress, when use wider and deep drinkers rather narrowed drinkers during high temperature. Researches were found that during the lower temperature broilers consume 2–3 mL water for 1 g of feed while at high temperatures it increases to 4–5 mL. In addition, assigning enough number of drinkers, increase watering space for birds, placing water storage tank in the shade, ensuring sufficient water flow (>70 mL/min/nipple), withdrawing chlorination process during high temperature are some of strategies can be applied to mitigate the heat stress in broilers.

3.5.1 Increase the access to cold water

Some of researches have investigated that giving cold water to heat-stressed broiler birds caused to ameliorate the negative effects and improved feed intake, body weight gain, increased performance, dressing percentage, relative weight of gizzard, liver, enhance meat juiciness, tenderness and reduced body temperature, tonic immobility, and total antioxidant capacity and lower malonaldehyde concentration in broiler chicken [107, 108]. Further it was recommended to supply ice added water to keep body temperature in stable less than 25°C.

3.6 Nutritional management to attenuate the heat stress

Nutritional management has become effective to minimize the deleterious effects of heat in poultry production. Supplementation with some feed additives, minerals, and vitamins into broiler diets has shown to partially mitigate the negative effects of HS including mortality. Out of different nutritional methods that are more frequently adopted are: vitamin and mineral handling, modification of the electrolyte balance of the feed among others. Multiple studies have shown supplementation of vitamin E and vitamin C reduced the adverse effects of chronic HS on performance. Ref. [109] suggested the use of non-chloride salts, such as sodium bicarbonate, more effective to reduce the negative effects of heat stress through an improved balance of electrolytes.

3.6.1 Supply dietary electrolytes and minerals

Sodium (Na), potassium (K) and chlorine (Cl) are key mineral elements involved in the maintenance of the acid-base balance of body fluids. The beneficial effects of supplementing the feed or drinking water of heat stressed poultry with compounds of these minerals such as ammonium chloride (NH4Cl), sodium bicarbonate (NaHCO3), sodium chloride (NaCl), potassium chloride (KCl), and potassium sulfate (K2SO4) are well documented such as enhancement of immune responses, nutrient digestibility [34, 79, 110]. In addition, Table 2 explains effect of dietary electrolytes and minerals to overcome the heat stress in broilers.

Type of mineralConcentrationEffect on heat-stressed broilersReference
NaHCO35 g/kgIncreased body weight gain of 9%[111]
Na, K, and Cl saltsIncreased water consumption facilitates heat dissipation normalization of blood electrolyte balance[111]
KCl0.2–0.5% in waterMaintain osmotic and acid base balance increased water consumption[112]
NaHCO34–10 kg/t feedRestore the acid-base balance lost in alkalosis[111]
KСl0.25–0.5% in drinking water or 0.5–1.0% in feedRestores the electrolyte balance
Retain more electrolytes (Na, K, Cl)
Maintain the acid-base balance
[82]
NH4Cl
KCl
KCl
NaHCO3
0.2% or
0.15%,
0.6%,
0.2% and carbonated water in drinking water
Enhanced growth performance[34]
Zn40 mg Zn/kg of feedImproved growth rate, FCR, and antioxidant enzymes and minimized lipid peroxidation in broilers raised in heat stress conditions[113]
4.5 mg/kg of feedImproved the performance of the heat-stressed broiler[114]
Organic SeAt 0.3 mg/kg dietEnhanced live body weight and feed conversion ratio[115]
Magnesium and Zn600 mg magnesium and 30 mg zinc/kg dietIncreased live BW, FI, and dressing percentage in Japanese quail under heat stress conditions.[116]
KCl, NaCl0.4% KCl or 0.4% sodium chloride (NaCl) to drinking waterImproved BW, FI, and FCR[117]
Chromium120 ppb chromiumImproved the performance of the heat-stressed broiler[118]
600 mg/kg or (400 mg/kg) with 250 mg/kg vitamin CIncreases the bodyweight of broilers
Selenium0.4–1 mg/kgEnhanced growth performance of broilers, improved DNA synthesis, enhanced cellular antioxidant levels and immune system responses[119, 120]

Table 2.

Effect of dietary electrolytes and minerals to overcome the heat stress in broilers.

In addition, Refs. [113, 121] elaborated that the significant effects of minerals such as selenium, chromium, zinc, etc. on the improvement of performance parameters and reduction in heat shock proteins, the requirement of phosphorous and calcium increases during HS in broiler chicken reared in tropical climates.

The dietary supplementation of selenium increased growth performance, immune responsiveness and provision of organic selenium enhanced antioxidant capability, productive and reproductive performances in Japanese quails and broiler roosters [120, 122]. Moreover, incorporating organic zinc to the heat-stressed broiler diet, investigated that enhancement of growth, digestibility, antioxidative status, humoral immune responsiveness and decreased lipid oxidation in meat extracted from heat-stressed broilers.

Ref. [123] observed that the feeding of dietary amino acid-chelated minerals such as Fe, Mn, Co, Zn, Cu, Mg, K, and Ca decreased serum and intestinal HSP70 and gene expression of pro inflammatory cytokines in heat-stressed broilers. Ref. [124] were revealed that the dietary requirement of potassium (0.6–0.7%), sodium (0.20–0.25%), chloride (0.30%) levels were increased with increase in temperature and the precise electrolyte balance and electrolyte ratio (EB of 350 mEq/kg and an ER of 3) improved broiler performance, livability and prevented the negative effects of HS.

3.6.2 Supplementation of dietary vitamins to the heat-stressed broilers

The supplementation of Vitamin A, B, D, C, and E reasoned to attenuate the effect of HS in broilers and improved the performance, feed intake, immune functions, reduced respiratory quotient, body temperature, carcass weight, nutrient utilization, and protein content of meat during the high temperature [39, 103, 125, 126, 127, 128].

Ref. [114] explored that the broiler diets which contained vitamin A protected the tissues against damages due to oxidation, increased weight gain and feed efficiency.

Ref. [129] recommended adding (vitamin C) VC at 1 g/L of drinking water throughout heat periods and addition of VC to the drinking water declined corticosterone. Further, VC declined metabolic rates, enhanced antioxidant activity, reduced lipid oxidation, increased performance in heat stressed Japanese quails and Ref. [130] ensured that the addition of VC 250 mg/kg of feed increased feed conversion efficiency, high growth performances, survival rate, and carcass quality of broiler chicken effected from HS.

An experiment based on vitamin E (VE) fortification in the rate of 200 mg/kg for heat-stressed broilers confirmed that increased phagocytic activities of macrophages, enhanced serum antibodies (IgM and IgG) levels, growth performances, increment of carcass and cuts yield, lower lipid peroxidation in chicken semen, increased antioxidant capacity, increased activity of the glutathione peroxidase, catalase, superoxide dismutase and glutathione reductase in erythrocytes [119, 122, 131]. Further Ref. [132] elaborated that aforesaid VE level helped to reduce the effect of incidences of Pale, Soft, Exudative meat from HS broilers.

Ref. [133] confirmed that supplementation of VE 100 IU/kg feed, enhanced number of T-lymphocytes and SRBC (sheep red blood cells) antibodies, spleen weight, and bursa of Fabricius, reduced the activity of stress hormones and it helped to safeguard lymphocytes, macrophages and plasma cells contrary to oxidative impairment, enhanced immune responses, etc. in heat-stressed birds [134, 135]. Further, provision of 250 mg VE/kg caused to increase the action of GSH-Px and declined the expression of heat shock protein-60 (HSP60) and improved meat quality in heat-stressed broilers [128].

Correspondingly, Ref. [136] investigated that the combination of 100 mg/kg of vitamin E + 50 mg/kg zinc is a strategy for broilers reared under HS, as it favors the growth performance. Moreover addition of electrolytes such as sodium bicarbonate with vitamins E and C in to the diet of broilers reared under heat stress caused to increase feed conversion ratio, plasma calcium level from 7 to 35 days. Synergistic effects of vitamins made higher efficiency rather than single form of vitamin such as VC at 200 mg/kg or VE at 150 mg/kg reasoned to enhance semen quality and fertility of broiler roosters was identified by Ref. [137]

3.6.3 Alter the composition of diet changing energy and protein concentration

Poultry kept under HS, make effort to regulate body temperature by lowering intake of energy. Ref. [79] suggested that feeding of diet which contained increased energy level would be beneficial for the heat-stressed broilers. Further some of authors recommended to feed high proteins with moderate energy levels also a good solution and contradictorily, Refs. [138, 139, 140] advocated that inclusion of increased level of fat by incorporating coconut oil or beef tallow caused to enhance the heat tolerability, body weight gain, and feed conversion efficiency, of broilers. Similarly, in high temperatures (32–39°С) feeding broilers with low crude protein but rich with essential amino acids and high metabolizable energy containing diet showed higher efficacy rather than high crude protein and same level of energy fortified diet was investigated by Ref. [141]

3.6.4 Regulate the amino acid composition in the broiler diet

National Research council confirmed that broiler feed must be articulated with 100% digestible amino acids which directly target to the requirement of broiler production. There was a suggestion to adjust the crude protein levels according to the requirement of essential amino acids of broilers can be reduced the heat production during the amino acid oxidation. Different researchers had conducted numerous researches based on reduced crude protein levels for broilers in constant heat stress [43], cyclic heat stress [43, 71, 142], and hot climates [137, 141].

In addition, Attia et al. [137] defined that supplementation of Lysine with Methionine in a diet which has lower crude protein level could be able to balance the same performances and carcass characters of the heat-stressed broilers as the diet of high crude protein level. Similarly Ref. [143] verified that enhanced feed conversion efficiency and some of wellbeing signs from Pekin ducks exposed to HS by supplementation of arginine. Further, Ref. [144] investigated that Trypsin supplementation decreased rectal temperature, corticosterone responses, and some other authors confirmed that by balancing the essential amino acids levels in a ration could reduce the energy cost need to evacuate the additional nitrogen and it would support the chicken to cope with HS.

Moreover, Ref. [145] investigated that adding 1% of Glutamine to the diet of heat-stressed broilers caused to increased growth performances, development of intestinal environment and humoral immunity. Similarly Ref. [44] confirmed that adding Glutamine to the broiler diet reduced the effect of HS by regulating the intestinal barrier functions such as cell proliferation in intestine, secretion of cytokines, amending the tight junction proteins. Subsequently, Cystein and Methinine incorporated broiler diet could be enhanced the growth performance, lower rectal temperature in heat-stressed broilers.

3.6.5 Adding fat in to the diet

Fat generates lower amount of heat rather than protein and carbohydrate at metabolism is a standard statement. Thus some researchers suggested increasing the fat level up to 5% reasoned to decline stress made by the heat on broilers. Incorporation of dietary omega-3 fatty acids ameliorated the effect of HS by increasing antioxidant status and antibody responsiveness, reducing lipid peroxidation in Japanese quails reared in high temperature and stated that it caused to enhance growth and performance index of heat-stressed broiler chicken [146].

3.6.6 Use of feed additives to decline the effect of heat stress

Some of researchers have identified that the value of incorporating Betaine enhanced ion balance, immunity, Methionine sparing, fat circulation, and developed a resistance against heat stress [135, 147].

3.6.6.1 Feeding probiotics for heat-stressed broilers

Probiotics enhanced the serum T3 and T4 levels, functions of immune system, responses of antibody levels, leucocytes count, decline corticosterone, increment of intestinal morphology in heat-stressed broilers [17, 148]. Further, probiotic fortified diet could increase the growth performance, feed conversion ratio and immune responses in heat-stressed broilers. In addition the protection of skeletal muscle quality and increased breast meat weight were experienced by giving probiotic incorporated diet to heat-stressed broilers. Provision of Bacillus subtilis, Lactobacillus, L. pentosus, L. acidophilus like probiotics encouraged the protection of lymphoid organs from heat damages, increased production performance, behaviors and immunity, augmenting the multiplicity of flora in the jejumum and cecum, enhance the growth performances, ameliorate the manifestation of four sugar transporter genes (GLUT2, GLUT5, SGLT1, and SGLT4), increment of fatty acid profile in meat in heat-stressed broilers [149].

The mixture of mannan-oilgosachcharides, prebiotics and probiotics influenced on increment of performance, welfare aspects, morphology of intestine, immune responses of heat-stressed broilers and enhanced aforesaid parameters were detected by researchers.

3.6.6.2 Incorporation of exogenous enzymes in to the diet

The dietary exogenous enzyme mixtures assorted broiler feed caused to increase palatability of feed, digestibility of nutrients, reduction of feed cost, enhance the growth performance of heat-stressed broilers [34, 82]. In addition, provision of bile acids enhanced the weight gain, feed conversion efficiency, antioxidant capability, and upheld homeostasis in the gut-liver axis [150].

3.6.6.3 Supplementation of ordinary antioxidants

The incorporation of natural antioxidants to the diet of heat-stressed broilers is an efficient strategy to overcome the adverse effects of high temperature during the rearing period and scientists have proved that this is due to discharging action on free radicals derived from heat stress. Different authors have explained about their findings related to the numerous antioxidant types such as tocopherols, ascorbic acid, carotenoids, flavonoids, non-flavonic phenols, Se, Zn, Cu, and Mn like minerals, etc. [5, 79].

3.6.6.4 Incorporate photobiotic to the broiler diet

Plant originated naturally presented bio active compounds are useful as the form of phytogenic feed additives and they efficiently perform as accepted antioxidants when integrate in to broiler diet such as Curcumin, Ginger, Epigallocatechin Gallate, Resveratrol and Lycopene, etc. [151, 152]. Moreover, Table 3 elaborates, benefits of natural herbs to mitigate the heat stress in broilers.

Type of herbInclusion level and available compoundsEffect on heat-stressed broilersReferences
Ginger2%
  • Increased biochemical blood parameters

  • Enhanced growth performance

  • High antibacterial potential

  • Increment of the digestibility, palatability, metabolism, and health status of broilers

[134, 153]
Fermented dried ginger1%
  • Lower abdominal fat

  • Enhance the health

[154]
Garlic2 and 4 g/kg
  • Increase intestinal villi

  • Reduce crypt depth

[155]
Garlic powder incorporated probiotic and citric acid
  • Increased feed utilization

  • Ameliorate antioxidant status and humoral immunity

[156]
Nigella sativa (black seed)Thymoquinone, nigellone, and thymohydroquinone
2%
  • Increase antitoxic and antimicrobial properties

  • Higher defense mechanisms against infectious diseases

  • Weight gain in pigeon and body weight enhancement

  • Protect from formation of hepatic lesion, mild vascular congestion and vacuolization of the hepatocyte

[157]
[158]
Black seed1%
  • High the feed intake

  • Increased dressing percentage

  • High body gain

  • Decline the panting behavior

  • Declined water to feed ratio, corticosterone, and T3 levels

[159]
Black seed5.6%
  • Increased BW, BWG, FI and FCR

[160]
Anthocyanins
  • Antioxidant, anti-inflammatory

  • Immunomodulatory

  • Antidiabetic

  • Anti-obesity

  • Neuroprotective and anticancer biochemical agents

[147]
Lycopene200 or 400 mg lycopene/kg
  • Powerful antioxidant

  • Increase cell growth and the immune response

  • Natural anti-stressor

  • Lessen adverse impacts of heat stress

  • Anti-inflammatory, immune-booster effect

  • Better performance and enhanced meat quality parameters

  • Augment antioxidant enzymes such as SOD and GSH-Px

  • Dropping MDA level

  • Boosted FI, BW and FCR

  • Upgraded meat quality characterizes

[161, 162, 163]
[164]
[164]
[165]
[162]
[162]
[165]
Curcumin derived from turmeric100 mg curcumin/kg
200 or 400 mg/kg diet
Japanese quail broilers
  • Antioxidative and anti-inflammatory properties

  • Amplified growth performance

  • Superior antioxidant biomarkers

  • Immune-related gene expressions

  • Higher final BW

  • Diminished the mitochondrial MDA concentration

  • Lessened ROS production through activating GSH-Px, SOD and glutathione S-transferase and enhancing gene expression of peroxiredoxin-3 and thioredoxin-2

  • Amplified BW, FI and

  • Declined serum lipid peroxidation and HSP70

[166]
[152]
[152]
[167]
Resveratrol (trans-3,5,4′-trihidroxiestilbeno)300–500 mg/kg of feed
  • Improvement in FI and BWG in chickens under chronic heat stress (37°C for 15 days)

  • Lower HSP27, HSP70, and HSP90 mRNA in spleen and bursa of Fabricius

  • Advancement in the low mRNA expression of HSP27 and HSP90 in thymus

  • Upgrading of antioxidant enzymes SOD, CAT, and GSH-Px

  • Diminished MDA

  • Renovating the dislocated villus-crypt structure due to heat stress

  • Repair of the normal intestinal microflora (amplified Lactobacillus and Bifidobacterium and lessened Escherichia coli)

  • Enhanced the intestinal epithelial barrier function and tight junction via modulating the mRNA expression of related genes

[168]
[68]
[112]
Epigallocatechin-3-gallate (EGCG)from green tea300 or 600 mg EGCG/kg diet
  • Upgraded growth performance

  • Enhanced antioxidant enzymes (CAT, SOD, and GSH-Px) in the liver and plasma

  • Reduced oxidative stress

[151]
[169]
Rosemary
Purified rosemary extract
0.4%
  • Improved growth performance

  • Amplified cecal microbiological populations and fat accumulation

  • Motivation of crystallin alpha B and HSP70

[170]
Cinnamon powder0.5%
  • Enhanced daily gain and antioxidative status (SOD,CAT, and total antioxidant capacity)

  • Decline the concentrations of MDA

[171]
Thyme essential oil150 and 200 mg/kg
  • Improved growth performance,

  • Augmented humoral immune response, and relative weight of lymphoid organs (spleen, thymus, and bursa of Fabricius)

Onion
Quercetin
Allicin
2.5 onion kg/t as a powder +2.5% onion extract in drinking water
  • BWG and FCR

  • Encouraged heat tolerance

  • Eradicate the free radicals,

  • Preserve and regenerate vitamin E and prevent the deleterious effects of chelate metal ions

  • Improved antimicrobial activity

  • Upgraded growth performances

[172]
Essential oils
  • Curcuma xanthorrhiza

  • Oreganum compactum

  • Orange peel extract

  • Decline the oxidative stress in broilers under cyclic and chronic heat stress

[173]
Dried plum (Prunus domestica L.)2.5%
  • Enhanced the growth performance

  • Expression of heat shock protein-related, antioxidant related, immune related, ileum histomorphology and tight-junction related genes

  • Enhanced intestinal integrity

  • Amplified butyrate along with total VFAs concentration in the cecum

  • Improved the relative abundance of beneficial bacteria in the cecum

[25]

Table 3.

Benefits of natural herbs to mitigate the heat stress in broilers.

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4. Conclusion

Considering the increment of environmental temperature, it is essential to identify the adverse effects of high ambient temperature on broilers. Various up-to-date studies are being published in relation to heat stress in broilers, effect of heat stress on different roles of broiler bird and the way of influence to the broiler industry and numerous mitigation strategies to overcome the major issues related to the heat stress. Among the discussed evidences, nutritional management represents higher efficiency compared to the other alleviation techniques of HS. Thus it is a promising topic that needs to focus in broiler industry while introducing updated knowledge to the stakeholders of the industry.

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Conflict of interest

The authors declare no conflict of interest.

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Appendices and nomenclature

AST

aspartate aminotransferase

BWG

body weight gain

CNS

central nervous system

Cr

chromium

FI

feed intake

FAO

Food and Agriculture Organization

GnRH

hypothalamic gonadotropin-releasing hormone

GIT

gastrointestinal tract

H:L

heterophil to lymphocyte ratio

LH

luteinizing hormone

HSP

heat shock protein

HS

heat stress

PCV

packed cell volume

References

  1. 1. Diarra SS, Tabuacir P. Feeding management of poultry in high environmental temperatures. International Journal of Poultry Science. 2014;13(11):657-661. ISSN 1682-8356 © Asian Network for Scientific Information
  2. 2. Suganya T, Senthilkumar S, Deepa K, Amutha R. Nutritional management to alleviate heat stress in broilers. International Journal of Science Environment and Technology. 2015;4:661-666
  3. 3. Mack LA, Felver-Gant JN, Dennis RL, Cheng HW. Genetic variations alter production and behavioral responses following heat stress in 2 strains of laying hens. Poultry Science. 2013;92:285-294. DOI: 10.3382/ps.2012-02589
  4. 4. Sohail MU, Hume ME, Byrd JA, Nisbet DJ, Ijaz A, Sohail A, et al. Effect of supplementation of prebiotic mannan-oligosaccharides and probiotic mixture on growth performance of broilers subjected to chronic heat stress. Poultry Science. 2012;91:2235-2240
  5. 5. Abdel-Moneim AE, Elbaz AM, Khidr RE, Badri FB. Effect of in ovo inoculation of Bifidobacterium spp. on growth performance, thyroid activity, ileum histomorphometry and microbial enumeration of broilers. Probiotics and Antimicrobial Proteins. 2020;12:873-882
  6. 6. Raza S, Abdelnour S, Dhshan A, Hassanin A, Noreldin A, Albadrani G, et al. Potential role of specific microRNAs in the regulation of thermal stress response in livestock. Journal of Thermal Biology. 2021;96:102859
  7. 7. Oke OE, Alo ET, Oke FO, Oyebamiji YA, Ijaiya MA, Odefemi MA, et al. Early age thermal manipulation on the performance and physiological response of broiler chickens under hot humid tropical climate. Thermal Biology. 2020;88:102517. DOI: 10.1016/j.jtherbio.2020.10251
  8. 8. Kpomasse CC, Oke OE, Houndonougbo FM, Tona K. Broiler production challenges in the tropics: A review. Veterinary Medicine and Science. 2021;7(3):831-812
  9. 9. Nardone A, Ronchi B, Lacetera N, Ranieri MS, Bernabucci U. Effects of climate change on animal production and sustainability of livestock systems. Livestock Science. 2010;130:57-69
  10. 10. Dayyani N, Bakhtiyari H. Heat stress in poultry: Background and affective factors. International Journal of Advanced Biological and Biomedical Research. 2013;1(11):1409-1413
  11. 11. Ranjan A, Sinha R, Devi I, Rahim A, Tiwari S. Effect of heat stress on poultry production and their managemental approaches. International Journal of Current Microbiology and Applied Sciences. 2019;8(02):1548-1555. ISSN: 2319-7706
  12. 12. Bahrami A, Moeini MM, Ghazi SH, Targhibi MR. The effect of different levels of organic and inorganic chromium supplementation on immune function of broiler chicken under heat-stress conditions. Journal of Applied Poultry Research. 2012;21:209-215. DOI: 10.3382/japr.2010-00275
  13. 13. Marchini CFP, Café MB, Araújo EG, Nascimento MRBM. Physiology, cell dynamics of small intestinal mucosa, and performance of broiler chickens under heat stress: A review. Revista Colombiana de Ciencias Pecuarias. 2016;29(3):159-168
  14. 14. Oke OE. Evaluation of physiological response and performance by supplementation of Curcuma longa in broiler feed under hot humid tropical climate. Tropical Animal Health and Production. 2018;50(5):1071-1077. DOI: 10.1007/s11250-018-1532-8
  15. 15. Wan X, Ahmad H, Zhang L, Wang Z, Wang T. Dietary enzymatically treated Artemisia annua L. improves meat quality, antioxidant capacity and energy status of breast muscle in heat-stressed broilers. Journal of the Science of Food and Agriculture. 2018;98(10):3715-3721
  16. 16. Virden WS, Kidd MT. Physiological stress in broilers: Ramifications on nutrient digestibility and responses. Journal of Applied Poultry Research. 2009;18:338-347. DOI: 10.3382/japr.2007-00093
  17. 17. Sohail MU, Ijaz A, Yousaf MS, Ashraf K, Zaneb H, Aleem M, et al. Alleviation of cyclic heat stress in broilers by dietary supplementation of mannanoligosaccharide and Lactobacillus-based probiotic: Dynamics of cortisol, thyroid hormones, cholesterol, C-reactive protein, and humoral immunity. Poultry Science. 2010;89:1934-1938. DOI: 10.3382/ps.2010-00751
  18. 18. Etches RJ, John TM, Gibbins AV. Behavioural, physiological, neuroendocrine and molecular responses to heat stress. Poultry Production in Hot Climates. 2008;2:48-79
  19. 19. NRC. Nutrient requirements of poultry. 9th revised ed. Washington, D.C., USA: National Academy Press; 1994
  20. 20. Yahav S. Domestic fowl-strategies to confront environmental conditions. Avian and Poultry Biology Reviews. 2000;11:81-95
  21. 21. Imik H, Ozlu H, Gumus RE, Atasever MA, Urcar S, Atasever M. Effects of ascorbic acid and α-lipoic acid on performance and meat quality of broilers subjected to heat stress. British Poultry Science. 2012;53(6):800-808
  22. 22. Zhang ZY, Jia GQ , Zuo JJ, Zhang Y, Lei J, Ren L, et al. Effects of constant and cyclic heat stress on muscle metabolism and meat quality of broiler breast fillet and thigh meat. Poultry Science. 2012;91(11):2931-2937
  23. 23. Vecerek V, Voslarova E, Conte F, Vecerkova L, Bedanova I. Negative trends in transport-related mortality rates in broiler chickens. Asian-Australasian Journal of Animal Sciences. 2016;29:1796-1804
  24. 24. Liu L, Ren M, Ren K, Jin Y, Yan M. Heat stress impacts on broiler performance: A systematic review and meta-analysis. Poultry Science. 2020;99:6205-6211. DOI: 10.1016/j.psj.2020.08.019
  25. 25. Wasti S, Sah N, Singh AK, Lee CN, Jha R, Mishra B. Dietary supplementation of dried plum: A novel strategy to mitigate heat stress in broiler chickens. Journal of Animal Science and Biotechnology. 2021;12:1-7
  26. 26. de Souza LF, Espinha LP, de Almeida EA, Lunedo R, Furlan RL, Macari M. How heat stress (continuous or cyclical) interferes with nutrient digestibility, energy and nitrogen balances and performance in broilers. Livestock Science. 2016;192:39-43
  27. 27. Awad EA, Zulkifli I, Soleimani AF, Law FL, Ramiah SK, Mohamed-Yousif IM, et al. Response of broilers to reduced-protein diets under heat stress conditions. World's Poultry Science Journal. 2019;75(4):583-598
  28. 28. Deeb N, Cahaner A. Genotype by environment interaction with broiler genotypes differing in growth rate. 3. Growth rate and water consumption of broiler progeny from weightselected versus non selected parents under normal and high ambient temperatures. Poultry Science. 2002;81:293-330
  29. 29. Shakeri M, Cottrell JJ, Wilkinson S, Ringuet M, Furness JB, Dunshea FR. Betaine and antioxidants improve growth performance, breast muscle development and ameliorate thermoregulatory responses to cyclic heat exposure in broiler chickens. Animals. 2018;8(10):162
  30. 30. Lu Q , Wen J, Zhang H. Effect of chronic heat production, anion carriers and substrate oxidation exposure on fat deposition and meat quality in two in skeletal muscle mitochondria of heat-stressed genetic types of chicken. Poultry Science. 2007;86:1059-1064
  31. 31. North MO, Bell DD. Commercial Chicken Production Manual. 4th ed. New York, NY: Van Nostrand Reinhold; 1990. p. 262
  32. 32. Mujahid A, Sato K, Akiba Y, Toyomizu M. Acute heat stress stimulates mitochondrial superoxide production in broiler skeletal muscle, possibly via downregulation of uncoupling protein content. Poultry Science. 2006;85(7):1259-1265
  33. 33. Mujahid A, Yoshiki Y, Akiba Y, Toyomizu M. Superoxide radical production in chicken skeletal muscle induced by acute heat stress. Poultry Science. 2005;84(2):307-314
  34. 34. Lin H, Decuypere E, Buyse J. Acute heat stress induces oxidative stress in broiler chickens. Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology. 2006;144(1):11-17
  35. 35. Mujahid A. Nutritional strategies to maintain efficiency and production of chickens under high environmental temperature. The Journal of Poultry Science. 2011;48(3):145-154
  36. 36. Akbarian A, Golian A, Kermanshahi H, Farhoosh R, Raji AR, De Smet S, et al. Growth performance and gut health parameters of finishing broilers supplemented with plant extracts and exposed to daily increased temperature. Spanish Journal of Agricultural Research. 2013;11(1):109-119
  37. 37. Geraert PA, Padilha JC, Guillaumin S. Metabolic and endocrine changes induced by chronic heatexposure in broiler chickens: Growth performance, body composition and energy retention. The British Journal of Nutrition. 1996;75(2):195-204
  38. 38. Sahin N, Hayirli A, Orhan C, Tuzcu M, Akdemir FA, Komorowski JR, et al. Effects of the supplemental chromium form on performance and oxidative stress in broilers exposed to heat stress. Poultry Science. 2017;96(12):4317-4324
  39. 39. Attia YA, Al-Harthi MA, El-Shafey AS, Rehab YA, Kim WK. Enhancing tolerance of broiler chickens to heat stress by supplementation with vitamin E, vitamin C and/or probiotics. Annals of Animal Science. 2017;17(4):1155-1169
  40. 40. Wickramasuriya SS, Kim E, Cho HM, Shin TK, Kim B, Lee M, et al. Differential effects of dietary methionine isomers on broilers challenged with acute heat stress. The Journal of Poultry Science. 2019;56(3):195-203
  41. 41. Bogin E, Avidar Y, Pech-Waffenschmidt V, Doron Y, Israeli BA, Kevkhayev E. The relationship between heat stress, survivability and blood composition of the domestic chicken. European Journal of Clinical Chemistry and Clinical Biochemistry. 1996;34:463-469
  42. 42. Tao X, Xin H. Acute synergistic effects of air temperature, humidity, and velocity on homeostasis of market–size broilers. Transactions of ASAE. 2003;46(2):491
  43. 43. Awad EA, Idrus Z, Soleimani Farjam A, Bello AU, Jahromi MF. Growth performance, duodenal morphology and the caecal microbial population in female broiler chickens fed glycine-fortified low protein diets under heat stress conditions. British Poultry Science. 2018;59(3):340-348
  44. 44. Habashy WS, Milfort MC, Adomako K, Attia YA, Rekaya R, Aggrey SE. Effect of heat stress on amino acid digestibility and transporters in meat-type chickens. Poultry Science. 2017;96(7):2312-2319
  45. 45. Song ZH, Cheng K, Zheng XC, Ahmad H, Zhang LL, Wang T. Effects of dietary supplementation with enzymatically treated Artemisia annua on growth performance, intestinal morphology, digestive enzyme activities, immunity, and antioxidant capacity of heat-stressed broilers. Poultry Science. 2018;97(2):430-437
  46. 46. Al-Zghoul MB, Saleh KM, Jaradat ZW. Expression of digestive enzyme and intestinal transporter genes during chronic heat stress in the thermally manipulated broiler chicken. Poultry Science. 2019;98(9):4113-4122
  47. 47. Hai L, Rong D, Zhang ZY. The effect of thermal environment on the digestion of broilers. Journal of Animal Physiology and Animal Nutrition. 2000;83(2):57-64
  48. 48. Orhan C, Kucuk O, Sahin N, Tuzcu M, Sahin K. Effects of taurine supplementation on productive performance, nutrient digestibility and gene expression of nutrient transporters in quails reared under heat stress. Journal of Thermal Biology. 2020;92:102668
  49. 49. Gu XH, Li SS, Lin H. Effects of hot environment and dietary protein level on growth performance and meat quality of broiler chickens. Asian-Australasian Journal of Animal Sciences. 2008;21(11):1616-1623
  50. 50. Dai SF, Gao F, Xu XL, Zhang WH, Song SX, Zhou GH. Effects of dietary glutamine and gamma-aminobutyric acid on meat colour, pH, composition, and water-holding characteristic in broilers under cyclic heat stress. British Poultry Science. 2012;53(4):471-481
  51. 51. Olivo R, Scares AL, Ida EI, Shimokomaki M. Dietary vitamin E inhibits poultry PSE and improves meat functional properties. Journal of Food Biochemistry. 2001;25(4):271-283
  52. 52. Aoyagi Y, Ohnishi T, Itoh S, Nakaya T. Effect of heat stress and L-ascorbic acid-2-phosphate magnesium on plasma and liver thiobarbituric acid reactive substances concentrations, and on liver protein carbonyl concentration in chicks. Japanese Poultry Science. 1997;34(1):63-66
  53. 53. Pearce SC, Mani V, Weber TE, Rhoads RP, Patience JF, Baumgard LH, et al. Heat stress and reduced plane of nutrition decreases intestinal integrity and function in pigs. Journal of Animal Science. 2013;91(11):5183-5193
  54. 54. Donoghue DJ, Krueger BF, Hargis BM, Miller AM, Halawani ME. Thermal stress reduces serum luteinizing hormone and bioassayable hypothalamic content of luteinizing hormone-releasing hormone in hens. Biology of Reproduction. 1989;41(3):419-424
  55. 55. Riaz A, Aleem M, Ijaz A, Saeed MA, Latif A. Effect of collection frequency on the semen quality of broiler breeder. British Poultry Science. 2004;45(6):823-827
  56. 56. Noiva RM, Menezes AC, Peleteiro MC. Influence of temperature and humidity manipulation on chicken embryonic development. Veterinary Research. 2014;10:2-10
  57. 57. Kala M, Shaikh MV, Nivsarkar M. Equilibrium between anti-oxidants and reactive oxygen species: A requisite for oocyte development and maturation. Reproductive Medicine and Biology. 2017;16(1):28-35
  58. 58. Lambert GP. Stress-induced gastrointestinal barrier dysfunction and its inflammatory effects. Journal of Animal Science. 2009;87:E101-E108
  59. 59. Shin JE, Kim JH, Goo D, Han GP, Pitargue FM, Kang HK, et al. Effect of dietary supplementation of betaine on productive performance, egg quality and jejunal tight junction-related gene expression in laying hens raised under hot environmental conditions. Livestock Science. 2018;214:79-82
  60. 60. Quinteiro-Filho WM, Calefi AS, Cruz DSG, Aloia TPA, Zager A, Astolfi-Ferreira CS, et al. Heat stress decreases expression of the cytokines, avian beta-defensins 4 and 6 and toll-like receptor 2 in broiler chickens infected with Salmonella Enteritidis. Veterinary Immunology and Immunopathology. 2017;186:19-28. DOI: 10.1016/j.vetimm.2017.02.006
  61. 61. Bartlett JR, Smith MO. Effects of different levels of zinc on the performance and immune competence of broilers under heat stress. Poultry Science. 2003;82:1580-1588
  62. 62. Zulkifi I, Norma MT, Israf DA, Omar AR. The effect of early age feed restriction on subsequent response to high environmental temperatures in female broiler chickens. Poultry Science. 2000;79:1401-1407
  63. 63. Laganá C, Ribeiro AM, Kessler AD, Kratz LR, Pinheiro CC. Effect of the supplementation of vitamins and organic minerals on the performance of broilers under heat stress. Brazilian Journal of Poultry Science. 2007;9:39-43
  64. 64. Gomes AVS, Quinteiro-Filho WM, Ribeiro A, Ferraz-de-Paula V, Pinheiro ML, Baskeville E, et al. Overcrowding stress decreases macrophage activity and increases Salmonella Enteritidis invasion in broiler chickens. Avian Pathology. 2014;43:82-90
  65. 65. Santos RR, Awati A, Roubos-van den Hil PJ, Tersteeg-Zijderveld MH, Koolmees PA, Fink-Gremmels J. Quantitative histo-morphometric analysis of heat-stress-related damage in the small intestines of broiler chickens. Avian Pathology. 2015;44(1):19-22
  66. 66. Xiaofang H, Lu Z, Ma B, Zhang L, Li J, Jiang Y, et al. Chronic heat stress damages small intestinal epithelium associated with AMPK pathway in broilers. Journal of Agricultural and Food Chemistry. 2018;66:7301-7309
  67. 67. Zhang JF, Bai KW, Su WP, Wang AA, Zhang LL, Huang KH, et al. Curcumin attenuates heat stress induced oxidant damage by simultaneous activation of GSH-related antioxidant enzymes and Nrf2-mediated phase II detoxifying enzyme systems in broiler chickens. Poultry Science. 2018a;97:1209-1219
  68. 68. He J, He Y, Pan D, Cao J, Sun Y, Zeng X. Associations of gut microbiota with heat stress-induced changes of growth, fat deposition, intestinal morphology, and antioxidant capacity in ducks. Frontiers in Microbiology. 2019;10:423318
  69. 69. Mujahid A, Akiba Y, Toyomizu M. Progressive changes in the physiological responses of heat-stressed broiler chickens. The Journal of Poultry Science. 2009;46(2):163-167
  70. 70. Tan GY, Yang L, Fu YQ , Feng JH, Zhang MH. Effects of different acute high ambient temperatures on function of hepatic mitochondrial respiration, antioxidative enzymes, and oxidative injury in broiler chickens. Poultry Science. 2010;89(1):115-122
  71. 71. Liu JB, Liu ZQ , Chen L, Zhang HF. Effects of feed intake and dietary nutrient density on apparent ileal and total tract digestibility of nutrients and gross energy for growing pigs. Journal of Animal Science. 2016;94(10):4251-4258
  72. 72. Luo J, Song J, Liu L, Xue B, Tian G, Yang Y. Effect of epigallocatechin gallate on growth performance and serum biochemical metabolites in heat-stressed broilers. Poultry Science. 2018;97(2):599-606
  73. 73. Beckford RC, Ellestad LE, Proszkowiec-Weglarz M, Farley L, Brady K, Angel R, et al. Effects of heat stress on performance, blood chemistry, and hypothalamic and pituitary mRNA expression in broiler chickens. Poultry Science. 2020;99(12):6317-6325
  74. 74. Livingston ML, Pokoo-Aikins A, Frost T, Laprade L, Hoang V, Nogal B, et al. Effect of heat stress, dietary electrolytes, and vitamins E and C on growth performance and blood biochemistry of the broiler chicken. Frontiers in Animal Science. 2022;3:807267
  75. 75. Sahin K, Onderci M, Gursu MF, Kucuk O, Sahin N. Effect of melatonin supplementation on biomarkers of oxidative stress and serum vitamin and mineral concentrations in heat-stressed Japanese quail. Journal of Applied Poultry Research. 2004;13(2):342-348
  76. 76. Najafi P, Zulkifli I, Amat Jajuli N, Farjam AS, Ramiah SK, Amir AA, et al. Environmental temperature and stocking density effects on acute phase proteins, heat shock protein 70, circulating corticosterone and performance in broiler chickens. International Journal of Biometeorology. 2015;59:1577-1583
  77. 77. Khan RU, Naz S, Ullah H, Ullah Q , Laudadio V, Qudratullah, et al. Physiological dynamics in broiler chickens under heat stress and possible mitigation strategies. Animal Biotechnology. 2023;34(2):438-447
  78. 78. Kumar M, Ratwan P, Dahiya SP, Nehra AK. Climate change and heat stress: Impact on production, reproduction and growth performance of poultry and its mitigation using genetic strategies. Journal of Thermal Biology. 2021;97:102867
  79. 79. Wasti S, Sah N, Mishra B. Impact of heat stress on poultry health and performances, and potential mitigation strategies. Animals. 2020;10(8):1266
  80. 80. Abdel-Moneim AM, Shehata AM, Khidr RE, Paswan VK, Ibrahim NS, El-Ghoul AA, et al. Nutritional manipulation to combat heat stress in poultry—A comprehensive review. Journal of Thermal Biology. 2021;98:102915
  81. 81. Donald J. Getting the most from evaporative cooling systems in tunnel ventilated broiler houses. World Poultry. 2000;16:34-39
  82. 82. Shamsutdinova IR, Derkho MA. Changes in morphological parameters of the blood of laboratory animals when administered per os with silver nanoparticles. Agroindustrial complex of Russia. 2015;73:166-170
  83. 83. Esmail SHM. Thermal influences on poultry. Poultry World. 2001;17(3):26-27
  84. 84. Yahav S, Straschnow A, Luger D, Shinder D, Tanny J, Cohen S. Ventilation, sensible heat loss, broiler energy, and water balance under harsh environmental conditions. Poultry Science. 2004;83:253-258. DOI: 10.1093/ps/83.2.253
  85. 85. Fisinin VI, Kavtarashvili AS. Heat stress in poultry. II. Methods and techniques for prevention and alleviation. Agricultural Biology. 2015;4 (eng):431-443
  86. 86. Kavtarashvili AS, Kolokol'nikova TN. Metody profilaktiki. Materialy Mezhdunarodnogo veterinarnogo kongressa “Aktual'nye veterinarnye problemy v promyshlennom ptitsevodstve”. In: Proc. Int. Vet. Congress “Actual Veterinary Challenges in Commercial Poultry”. 2013. pp. 129-132
  87. 87. Arjona AA, Denbow DM, Weaver WD. Effect of heat stress early in life on mortality of broilers exposed to high environmental temperatures just prior to marketing. Poultry Science. 1988;67:226-231
  88. 88. Zaboli GR, Rahimi S, Shariatmadari F, Torshizi MAK, Baghbanzadeh A, Mehri M. Thermal manipulation during Pre and Post-Hatch on thermotolerance of male broiler chickens exposed to chronic heat stress. Poultry Science. 2016;96:478-485
  89. 89. Nawaz AH, Amoah K, Leng QY, Zheng JH, Zhang WL, Zhang L. Poultry response to heat stress: Its physiological, metabolic, and genetic implications on meat production and quality including strategies to improve broiler production in a warming world. Frontiers in Veterinary Science. 2021;8:699081
  90. 90. Patra BN, Bais RKS, Prasad RB, Singh BP. Performance of naked neck versus normally feathered coloured broilers for growth, carcass traits and blood biochemical parameters in tropical climate. Asian-Australasian Journal of Animal Sciences. 2002;15:1776-1783. DOI: 10.5713/ajas.2002.1776
  91. 91. Syafwan S, Kwakkel RP, Verstegen MWA. Heat stress and feeding strategies in meat type chickens. World's Poultry Science Journal. 2011;67:653674
  92. 92. Cardoso DM, Cardeal PC, Soares KR, Sousa LS, Castro FL, Araújo IC, et al. Feed form and nutritional level for rearing growing broilers in thermoneutral or heat stress environments. Journal of Thermal Biology. 2022;103:103159
  93. 93. Hosseini SM, Afshar M. Effect of diet form and enzyme supplementation on stress indicators and bone mineralisation in heat-challenged broilers fed wheat-soybean diet. Italian Journal of Animal Science. 2017;16(4):616-623
  94. 94. Santos RR, Awati A, Roubos-van den Hil PJ, van Kempen TA, Tersteeg-Zijderveld MH, Koolmees PA, et al. Effects of a feed additive blend on broilers challenged with heat stress. Avian Pathology. 2019;48(6):582-601
  95. 95. Uzum MH, Oral Toplu HD. Effects of stocking density and feed restriction on performance, carcass, meat quality characteristics and some stress parameters in broilers under heat stress. Revue de Médecine Vétérinaire. 2013;164(12):546-554
  96. 96. Yalcin S, Özkan S, Türkmut L, Siegel PB. Responses to heat stress in commercial and local broiler stocks. 1. Performance traits. British Poultry Science. 2001;42(2):149-152
  97. 97. Farghly MF, Mahrose KM, Galal AE, Ali RM, Ahmad EA, Rehman ZU, et al. Implementation of different feed withdrawal times and water temperatures in managing turkeys during heat stress. Poultry Science. 2018;97(9):3076-3084
  98. 98. Abu-Dieyeh ZH. Effect of chronic heat stress and long-term feed restriction on broiler performance. International Journal of Poultry Science. 2006;5(2):185-190
  99. 99. Teyssier JR, Brugaletta G, Sirri F, Dridi S, Rochell SJ. A review of heat stress in chickens. Part II: Insights into protein and energy utilization and feeding. Frontiers in Physiology. 2022;13:943612. DOI: 10.3389/fphys.2022.943612
  100. 100. Basilio V, De Vilarin M, Yahav S, Picard M. Early age thermal conditioning and a dual feeding program for male broilers challenged by heat stress. Poultry Science. 2001;80(1):29-36
  101. 101. Macleod MG, Dabutha LA. Diet selection by Japanese quail (Coturnix coturnix japonica) in relation to ambient temperature and metabolic rate. British Poultry Science. 1997;38:586-589
  102. 102. Yo T, Siegel PB, Faure JM, Picard M. Self-selection of dietary protein and energy by broilers grown under a tropical climate: Adaptation when exposed to choice feeding at different ages. Poultry Science. 1998;77:502-508
  103. 103. Kutlu HR. Influences of wet feeding and supplementation with ascorbic acid on performance and carcass composition of broiler chicks exposed to a high ambient temperature. Archives of Animal Nutrition. 2001;54(2):127-139
  104. 104. Dei HK, Bumbie GZ. Effect of wet feeding on growth performance of broiler chickens in a hot climate. British Poultry Science. 2011;52(1):82-85
  105. 105. Afsharmanesh M, Barani M, Silversides FG. Evaluation of wet-feeding wheat-based diets containing Saccharomyces cerevisiae to broiler chickens. British Poultry Science. 2010;51(6):776-783
  106. 106. May JD, Lott BD, Simmons JD. Water consumption by broilers in high cyclic temperatures: Bell versus nipple waterers. Poultry Science. 1997;76:944-947
  107. 107. Park SO, Park BS, Hwangbo J. Effect of cold water and inverse lighting on growth performance of broiler chickens under extreme heat stress. Journal of Environmental Biology. 2015;36:865-873
  108. 108. Farghly MF, Abd El-Hack ME, Alagawany M, Saadeldin IM, Swelum AA. Ameliorating deleterious effects of heat stress on growing Muscovy ducklings using feed withdrawal and cold water. Poultry Science. 2019;98(1):251-259
  109. 109. Borges SA, Da Silva AF, Majorka A, Hooge DM, Cummings KR. Physiological responses of broiler chickens to heat stress and dietary electrolyte balance (sodium plus potassium minus chloride, milliequivalents per kilogram). Poultry Science. 2004;83(9):1551-1558
  110. 110. Fouad AM, Chen W, Ruan D, Wang S, Xia WG, Zheng CT. Impact of heat stress on meat, egg quality, immunity and fertility in poultry and nutritional factors that overcome these effects: A review. International Journal of Poultry Science. 2016;15(3):81
  111. 111. Ahmad T, Sarwar M. Dietary electrolyte balance: Implications in heat stressed broilers. World's Poultry Science Journal. 2006;62(4):638-653
  112. 112. Zhang C, Zhao XH, Yang L, Chen XY, Jiang RS, Jin SH, et al. Resveratrol alleviates heat stress-induced impairment of intestinal morphology, microflora, and barrier integrity in broilers. Poultry Science. 2017;96:4325-4332. DOI: 10.3382/ps/pex266
  113. 113. Rao SR, Prakash B, Raju MV, Panda AK, Kumari RK, Reddy EP. Effect of supplementing organic forms of zinc, selenium and chromium on performance, anti-oxidant and immune responses in broiler chicken reared in tropical summer. Biological Trace Element Research. 2016;172:511-520
  114. 114. Kucuk O, Sahin N, Sahin K. Supplemental zinc and vitamin A can alleviate negative effects of heat stress in broiler chickens. Biological Trace Element Research. 2003;94:225-235
  115. 115. Rahimi SH, Farhadi D, Valipouri AR. Effect of organic and inorganic selenium sources and vitamin E on broiler performance and carcass characteristics in heat stress condition. Veterinary Research & Biological Products. 2011;24(2):25-35
  116. 116. Kucuk O. Zinc in a combination with magnesium helps reducing negative effects of heat stress in quails. Biological Trace Element Research. 2008;123:144-153
  117. 117. Dai SF, Wang LK, Wen AY, Wang LX, Jin GM. Dietary glutamine supplementation improves growth performance, meat quality and colour stability of broilers under heat stress. British Poultry Science. 2009;50(3):333-340
  118. 118. Sahin K, Sahin N, Onderci M, Gursu F, Cikim G. Optimal dietary concentration of chromium for alleviating the effect of heat stress on growth, carcass qualities, and some serum metabolites of broiler chickens. Biological Trace Element Research. 2002;89:53-64
  119. 119. Niu ZY, Liu FZ, Yan QL, Li WC. Effects of different levels of vitamin E on growth performance and immune responses of broilers under heat stress. Poultry Science. 2009;88(10):2101-2107
  120. 120. Habibian M, Ghazi S, Moeini MM. Effects of dietary selenium and vitamin E on growth performance, meat yield, and selenium content and lipid oxidation of breast meat of broilers reared under heat stress. Biological Trace Element Research. 2016;169:142-152
  121. 121. Leeson S, Summers JD. Nutrition of the Chicken. 4th ed. Guleph, Ont., Canada: University Books; 2001
  122. 122. Ebeid TA. Vitamin E and organic selenium enhances the antioxidative status and quality of chicken semen under high ambient temperature. British Poultry Science. 2012;53(5):708-714
  123. 123. Baxter MF, Greene ES, Kidd MT, Tellez-Isaias G, Orlowski S, Dridi S. Water amino acid-chelated trace mineral supplementation decreases circulating and intestinal HSP70 and proinflammatory cytokine gene expression in heat-stressed broiler chickens. Journal of Animal Science. 2020;98(3):049
  124. 124. Khattak FM, Acamovic T, Sparks N, Pasha TN, Joiya MH, Hayat Z, et al. Comparative efficacy of different supplements used to reduce heat stress in broilers. Pakistan Journal of Zoology. 2012;44(1):31-41
  125. 125. Ferket PR, Qureshi MA. Performance and immunity of heat-stressed broilers fed vitamin-and electrolyte-supplemented drinking water. Poultry Science. 1992;71(1):88-97
  126. 126. Kutlu HR, Forbes JM. Changes in growth and blood parameters in heat-stressed broiler chicks in response to dietary ascorbic acid. Livestock Production Science. 1993;36(4):335-350
  127. 127. Kadim IT, Al-Qamshui BH, Mahgoub O, Al-Marzooqi W, Johnson EH. Effect of seasonal temperatures and ascorbic acid supplementation on performance of broiler chickens maintained in closed and open-sided houses. International Journal of Poultry Science. 2008;7:655-660
  128. 128. Habibian M, Ghazi S, Moeini MM, Abdolmohammadi A. Effects of dietary selenium and vitamin E on immune response and biological blood parameters of broilers reared under thermoneutral or heat stress conditions. International Journal of Biometeorology. 2014;58:741-752
  129. 129. Daghir NJ. Nutritional strategies to reduce heat stress in broilers and broiler breeders. Lohmann Information. 2009;44(1):6-15
  130. 130. Shakeri M, Oskoueian E, Le HH, Shakeri M. Strategies to combat heat stress in broiler chickens: Unveiling the roles of selenium, vitamin E and vitamin C. Veterinary Sciences. 2020;7(2):71
  131. 131. Singh V, Aballay A. Heat-shock transcription factor (HSF)-1 pathway required for Caenorhabditis elegans immunity. National Academy of Sciences of the United States of America. 2006;103(35):13092-13097
  132. 132. Hashizawa Y, Kubota M, Kadowaki M, Fujimura S. Effect of dietary vitamin E on broiler meat qualities, color, water-holding capacity and shear force value, under heat stress conditions. Animal Science Journal. 2013;84(11):732-736
  133. 133. Rashidi AA, Gofrani F, Ivari Y, Khatibjoo A, Vakili R. Effect of dietary fat, vitamin E and zinc on immune response and blood parameters of broilers reared under heat stress. Research Journal of Poultry Science. 2010;3:32-38. DOI: 10.3923/rjpscience.2010.32.38
  134. 134. Khan R, Naz S, Nikousefat Z, Selvaggi M, Laudadio V, Tufarelli V. Effect of ascorbic acid in heat-stressed poultry. World's Poultry Science Journal. 2012;68:477-490
  135. 135. Attia YA, Bovera F, Abd El-Hamid AE, Tag El-Din AE, Al-Harthi MA, El-Shafy AS. Effect of zinc bacitracin and phytase on growth performance, nutrient digestibility, carcass and meat traits of broilers. Journal of Animal Physiology and Animal Nutrition. 2016;100(3):485-491
  136. 136. Hosseini-Mansoub N, Chekani-Azar S, Tehrani A, Lotfi A, Manesh M. Influence of dietary vitamin E and zinc on performance, oxidative stability and some blood measures of broiler chickens reared under heat stress (35 °C). Journal of Agrobiology. 2010;27(2):103
  137. 137. Attia YA, Bovera F, Wang J, Al-Harthi MA, Kim WK. Multiple amino acid supplementations to low-protein diets: Effect on performance, carcass yield, meat quality and nitrogen excretion of finishing broilers under hot climate conditions. Animals. 2020;10(6):973
  138. 138. Zulkifli I, Htin NN, Alimon AR, Loh TC, Hair-Bejo M. Dietary selection of fat by heat-stressed broiler chickens. Asian-Australasian Journal of Animal Sciences. 2007;20(2):245-251
  139. 139. Ghazalah AA, Abd-Elsamee MO, Ali AM. Influence of dietary energy and poultry fat on the response of broiler chicks to heat therm. International Journal of Poultry Science. 2008;7(4):355-359
  140. 140. Seifi K, Rezaei M, Yansari AT, Zamiri MJ, Riazi GH, Heidari R. Short chain fatty acids may improve hepatic mitochondrial energy efficiency in heat stressed-broilers. Journal of Thermal Biology. 2020;89:102520
  141. 141. Zaman QU, Mushtaq T, Nawaz H, Mirza MA, Mahmood S, Ahmad T, et al. Effect of varying dietary energy and protein on broiler performance in hot climate. Animal Feed Science and Technology. 2008;146(3-4):302-312
  142. 142. Soares KR, Lara LJ, da Silva Martins NR, e Silva RR, Pereira LF, Cardeal PC, et al. Protein diets for growing broilers created under a thermoneutral environment or heat stress. Animal Feed Science and Technology. 2020;259:114332
  143. 143. Zhu W, Jiang W, Wu LY. Dietary L-arginine supplement alleviates hepatic heat stress and improves feed conversion ratio of Pekin ducks exposed to high environmental temperature. Journal of Animal Physiology and Animal Nutrition. 2014;98(6):1124-1131
  144. 144. Badakhshan Y, Emadi L, Esmaeili-Mahani S, Nazifi S. The effect of L-tryptophan on the food intake, rectal temperature, and blood metabolic parameters of 7-day-old chicks during feeding, fasting, and acute heat stress. Iranian Journal of Veterinary Research. 2021;22(1):55
  145. 145. Perna S, Alalwan TA, Alaali Z, Alnashaba T, Gasparri C, Infantino V, et al. The role of glutamine in the complex interaction between gut microbiota and health: A narrative review. International Journal of Molecular Sciences. 2019;20(20):5232
  146. 146. Attia YA, Al-Harthi MA, Sh Elnaggar A. Productive, physiological and immunological responses of two broiler strains fed different dietary regimens and exposed to heat stress. Italian Journal of Animal Science. 2018;17:686-697
  147. 147. Saeed M, Babazadeh D, Naveed M, Arain MA, Hassan FU, Chao S. Reconsidering betaine as a natural anti-heat stress agent in poultry industry: A review. Tropical Animal Health and Production. 2017;49:1329-1338
  148. 148. Deng W, Dong XF, Tong JM, Zhang Q. The probiotic Bacillus licheniformis ameliorates heat stress-induced impairment of egg production, gut morphology, and intestinal mucosal immunity in laying hens. Poultry Science. 2012;91:575-582. DOI: 10.3382/ps.2010-01293
  149. 149. Wang WC, Yan FF, Hu JY, Amen OA, Cheng HW. Supplementation of Bacillus subtilis-based probiotic reduces heat stress-related behaviors and inflammatory response in broiler chickens. Journal of Animal Science. 2018;96(5):1654-1666
  150. 150. Yin C, Xia B, Tang S, Cao A, Liu L, Zhong R, et al. The effect of exogenous bile acids on antioxidant status and gut microbiota in heat-stressed broiler chickens. Frontiers in Nutrition. 2021;8:747136
  151. 151. Xue B, Song J, Liu L, Luo J, Tian G, Yang Y. Effect of epigallocatechin gallate on growth performance and antioxidant capacity in heat-stressed broilers. Archives of Animal Nutrition. 2017;71(5):362-372
  152. 152. Zhang J, Bai KW, He J, et al. Curcumin attenuates hepatic mitochondrial dysfunction through the maintenance of thiol pool, inhibition of mt DNA damage, and stimulation of the mitochondrial thioredoxin system in heat-stressed broilers. Journal of Animal Science. 2018b;96(3):867-879
  153. 153. Rehman Z, Chand N, Khan RU, Naz S, Alhidary IA. Serum biochemical profile of two broiler strains supplemented with vitamin E, raw ginger (Zingiber officinale) and L-carnitine under high ambient temperatures. South African Journal of Animal Science. 2019;48:935. DOI: 10.4314/sajas.v48i5.13
  154. 154. Khonyoung D, Yamauchi K, Buwjoom T, Maneewan B, Thongwittaya N. Effects of dietary dried fermented ginger on growth performance, carcass quality, and intestinal histology of heat-stressed broilers. Canadian Journal of Animal Science. 2012;92:307-317. DOI: 10.4141/cjas2011-129
  155. 155. Shewita RS, Taha AE. Effect of dietary supplementation of different levels of black seed (Nigella sativa L) on growth performance, immunological, hematological and carcass parameters of broiler chicks. World Academy of Science, Engineering and Technology. 2011;5:31325. Available from: https://www.revmedvet.com/artdes-us.php?id=1273
  156. 156. Elbaz AM, Ashmawy ES, Salama AA, Abdel-Moneim AM, Badri FB, Thabet HA. Effects of garlic and lemon essential oils on performance, digestibility, plasma metabolite, and intestinal health in broilers under environmental heat stress. BMC Veterinary Research. 2022;18(1):430
  157. 157. Forouzanfar F, Fazly Bazzaz BS, Hosseinzadeh H. Black cumin (Nigella sativa) and its constituent (thymoquinone): A review on antimicrobial effects. Iranian Journal of Basic Medical Sciences. 2014;17:929-938
  158. 158. Shoukary RDEL, Sayed RK, Hassan RI. Behavioral, hepato-morphological, and biochemical studies on the possible protective effect of black seed and water bath against change-mediated heat stress on pigeon. Journal of Basic and Applied Zoology. 2018;79:23. DOI: 10.1186/s41936-018-0035-5
  159. 159. El-Shoukary RDM, Darwish MHA, Abdel-Rahman MAM. Behavioral, performance, carcass traits and hormonal changes of heat stressed broilers feeding black and coriander seeds. Journal of Advanced Veterinary Research. 2014;4:97-101. Available from: https://advetresearch.com/index.php/AVR/article/view/79
  160. 160. Soliman ES, Hamad RT, Ahmed A. Prophylactic and immune modulatory influences of Nigella sativa Linn. in broilers exposed to biological challenge. Veterinary World. 2017;10(12):1447
  161. 161. Srivastava S, Srivastava AK. Lycopene; Chemistry, biosynthesis, metabolism and degradation under various abiotic parameters. Journal of Food Science and Technology-Mysore. 2015;52:41-53
  162. 162. Arain MA, Mei Z, Hassan FU, Saeed M, Alagawany M, Shar AH, et al. Lycopene: A natural antioxidant for prevention of heat-induced oxidative stress in poultry. World's Poultry Science Journal. 2018;74(1):89-100
  163. 163. Sun B, Ma J, Zhang J, Su L, Xie Q , Bi Y. Lycopene regulates production performance, antioxidant capacity, and biochemical parameters in breeding hens. Czech Journal of Animal Science. 2014;59(10):471-479
  164. 164. Palozza P, Parrone N, Simone R, Catalano A. Role of lycopene in the control of ROS mediated cell growth: Implications in cancer prevention. Current Medicinal Chemistry. 2011;18:1846-1860
  165. 165. Sahin K, Orhan C, Tuzcu M, et al. Lycopene activates antioxidant enzymes and nuclear transcription factor systems in heat-stressed broilers. Poultry Science. 2016;95(5):1088-1095
  166. 166. Moniruzzaman M, Min T. Curcumin, curcumin nanoparticles and curcumin nanospheres: A review on their pharmacodynamics based on monogastric farm animal, poultry and fish nutrition. Pharmaceutics. 2020;12(5):447
  167. 167. Sahin K, Orhan C, Tuzcu Z, Tuzcu M, Sahin N. Curcumin ameloriates heat stress via inhibition of oxidative stress and modulation of Nrf2/HO-1 pathway in quail. Food and Chemical Toxicology. 2012;50(11):4035-4041
  168. 168. Liu LL, He JH, Xie HB, Yang YS, Li JC, Zou Y. Resveratrol induces antioxidant and heat shock protein mRNA expression in response to heat stress in black-boned chickens. Poultry Science. 2014;93(1):54-62
  169. 169. Sahin K, Orhan C, Tuzcu M, Ali S, Sahin N, Hayirli A. Epigallocatechin-3-gallate prevents lipid peroxidation and enhances antioxidant defense system via modulating hepatic nuclear transcription factors in heat-stressed quails. Poultry Science. 2010;89(10):2251-2258
  170. 170. Petricevic V, Lukic M, Skrbic Z, Rakonjac S, Doskovic V, Petricevic M, et al. The effect of using rosemary (Rosmarinus officinalis) in broiler nutrition on production parameters, slaughter characteristics, and gut microbiological population. Turkish Journal of Veterinary and Animal Sciences. 2018;42(6):658-664
  171. 171. Sadeghi AA, Moghaddam M. The effects of turmeric, cinnamon, ginger and garlic powder nutrition on antioxidant enzymes’ status and hormones involved in energy metabolism of broilers during heat stress. Iranian Journal of Applied Animal Science. 2018;8(1):125-130
  172. 172. Al-Ramamneh D. Reduce heat stress in broiler by adding onion. Russian Agricultural Sciences. 2018;44:92-96
  173. 173. Akbarian A, Golian A, Kermanshahi H, De Smet S, Michiels J. Antioxidant enzyme activities, plasma hormone levels and serum metabolites of finishing broiler chickens reared under high ambient temperature and fed lemon and orange peel extracts and Curcuma xanthorrhiza essential oil. Journal of Animal Physiology and Animal Nutrition. 2015;99(1):150-162

Written By

Maleeka Nambapana and Dinesh Jayasena

Submitted: 06 June 2024 Reviewed: 06 June 2024 Published: 01 July 2024