| Literature DB >> 35720853 |
Zi-Long Liang1, Fan Chen1, Sungkwon Park2, Balamuralikrishnan Balasubramanian2, Wen-Chao Liu1.
Abstract
Heat stress has become a widespread concern in the world, which is one of the major environmental stressors and causes substantial economic loss in the rabbit industry. Heat stress leads to multiple damages to the health of rabbits, such as organ damage, oxidative stress, disordered endocrine regulation, suppressed immune function and reproductive disorders, ultimately, induces the decreased production performance and increased mortality. Nutritional approaches, including feeding strategies, adjusting feed formula, and supplementing vitamins, minerals, electrolytes, Chinese herbal medicines, and functional active substances to the feed, were reported to mitigate the detrimental effects of heat stress in rabbits. Therefore, elucidating the damage of heat stress to rabbits; proper management and nutritional approaches should be considered to solve the heat stress issue in rabbits. This review highlights the scientific evidence regarding the effects of heat stress on rabbit's immune function, endocrine, blood biochemical changes, antioxidant capacity and production performance, and the potential mitigation strategies of nutritional intervention to alleviate heat stress in rabbits; which could contribute to develop nutritional strategies in relieving heat stress of rabbits.Entities:
Keywords: heat stress; immune function; mitigation strategy; nutritional intervention; production; rabbit; redox status
Year: 2022 PMID: 35720853 PMCID: PMC9201964 DOI: 10.3389/fvets.2022.906084
Source DB: PubMed Journal: Front Vet Sci ISSN: 2297-1769
Figure 1Challenges and opportunities for the rabbit industry in the context of global warming-induced heat stress.
Figure 2Effects of heat stress on antioxidant capacity and related signaling pathway of rabbits. (A) Thermoneutral temperature. (B) Heat stress. (C) Nrf pathway-Induction of oxidative stress.
Figure 3Summarize the impacts of heat stress on rabbits.
The beneficial effects of nutritional strategies in heat-stressed rabbit.
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| Green and juicy food | – | Decrease heat stress and relieve thirst and diuresis, prevent rabbit coccidiosis and enteritis | ( |
| Ice water | – | The body weight ↑, feed intake and feed conversion rate ↑ | ( |
| Fat | 3,050 Kcal DE kg−1 of diet | Production performance (e.g., body weight, daily weight gain, litter size and weight, reduce pre-weaning mortality)↑ | ( |
| – | Improve the palatability of feed, the appetite ↑, feed intake and growth rate ↑ | ( | |
| Amino acid | 50–100 mg kg−1 of diet | Haemato-biochemical and reproductive indicators in male rabbits↑ | ( |
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| Vitamin C | 500 mg kg−1 of diet | (1) T3, T4 ↑cortisol and glucose levels, body temperature↓ | ( |
| 200 mg kg−1 of diet | (2) Corticosterone and MDA in blood ↓ | ( | |
| 200 mg kg−1 of diet | (3) Reverse the liver and kidney dysfunction | ( | |
| 200 mg kg−1 of BW | (4) mRNA and protein expression of HSP70 in liver and kidney tissues ↑ cortisol and leptin ↓, satiety signal ↑ | ( | |
| 1g L−1 in DW | (5) Productive and reproductive performance, oocyte maturation rate↑ | ( | |
| Vitamin E | 40 mg kg−1 of diet | (1) Semen quality; T3, T4 hormonal levels↑, body temperature and respiration rate↓. | ( |
| 320–640 mg kg−1 of diet | (2) T-AOC ↑ | ( | |
| 150 mg kg−1 of diet | (3) Semen quality, plasma glucose, high-density lipoprotein↑ plasma cholesterol and triglyceride ↓ | ( | |
| 100 mg kg−1 of diet | (4) Pregnancy rate, litter size, lipid metabolism, antioxidant capacity ↑ | ( | |
| Vitamin A | 750 IU of diet | (1) Antioxidant enzyme activity ↑, lipid peroxidation ↓ | ( |
| 1.2–1.5 times higher than NRC (1977) | (2) Skin temperature, rectal temperature and pulse ↓ | ( | |
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| NaHCO3 | 300 mg kg−1 of BW | (1) Dissolving mucus, invigorating the stomach, inhibiting acid and increasing appetite | ( |
| – | (2) Sodium↑ and respiratory alkali poisoning ↓ | ( | |
| 0.1–0.2% in DW | (3) Invigorate the stomach and regulate blood acid-base balance | ( | |
| KCl | – | (1) Maintains intracellular osmotic pressure and acid-base balance | ( |
| 0.3–0.5% in DW | (2) Relieve heat stress, replenish potassium loss, and maintain blood potassium concentration. | ( | |
| KHCO3 | – | (1) Maintain the blood potassium concentration and improve the HCO3- concentration | ( |
| 2.5% in diet | (2) Production performance and blood biochemical indexes ↑ | ( | |
| NH4Cl | 2% in DW | Recover the high blood pH value, regulate acid-base balance and prevent respiratory alkali poisoning | ( |
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| Zinc | 1.5 times higher than NRC (1977) | (1) Anti-heat stress agent, trace elements in milk ↑, litter size and weight ↑ | ( |
| 1 mg subcutaneous injection | (2) The lipid metabolism function ↑ | ( | |
| Chromium | 0.8–1.0 mg kg−1 of diet | (1) Alleviate the damage on testicular spermatogenic function testosterone, LH and FSH in serum ↑ | ( |
| 0.4 mg kg−1 of diet | (2) Daily gain and feed intake ↑, cellular immunity function ↑ | ( | |
| Selenium | 0.3 mg kg−1 of diet | (1) Rectal temperature ↓, serum total protein content, albumin content and GSH-Px activity ↑. The total protein, albumin, ALT, fructose and total antioxidant capacity ↑, MDA ↓ | ( |
| 25–50 mg kg−1 of diet | (2) Body weight and average daily gain ↑, GSH and CAT activities ↑and reduce MDA ↑ | ( | |
| Chinese herbal medicines | – | (1) Immunologic enhancement and antivirus action | ( |
| 20 mg injection | (2) Lymphocyte proliferation and antibody titer ↑ | ( | |
| 1–3% in diet | (3) Production performance, reproductive performance and antioxidant level ↑ | ( | |
| 1% in diet | (4) Mortality ↓ | ( | |
| 5% in diet | (5) Intestinal mucosa structure ↑ | ( | |
| 4.4 g in diet | (6) Sperm yield and survival rate ↑, sperm malformation rate ↓ | ( | |
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| L-Carnitine | 50 mg kg−1 of diet | (1) Rectal temperature, heart rate, and respiration rate ↓, growth indices, feed conversion ratio, blood hemoglobin, white blood cell counts, total protein, glucose, and red blood cell counts ↑ | ( |
| 100 mg kg−1 of diet | (2) Sperm motility, serum antioxidative status ↑ | ( | |
| Algae | 100 mg kg−1 of diet | (1) Production performance, antioxidants indices ↑, inflammatory responses and intestinal pathogens ↓ | ( |
| 300 mg kg−1 of diet | (2) Conception rate, kindling rate, litter size, embryo quality and the ovulatory response ↑ | ( | |
| Essential oils | 300 mg kg−1 of diet | Plasma testosterone concentration and GSH activity, sperm output, sperm cell counts, intact acrosome, sperm normality ↑, sperm cells with abnormal tail and plasma MDA contents ↓ | ( |
| 100–150 mg kg−1 of diet | Haemato-biochemicals constitutes, immunologic status, antioxidant capacity, and fertility traits ↑, lipid peroxidation ↓ | ( | |
| Plant extract | 100–300 mg kg−1 of diet | (1) Growth performance, carcass traits and antioxidant status ↑ | ( |
| 5–10 g kg−1 of diet | (2) Body weight, feed intake, SOD, T-AOC and GSH-Px ↑, MDA and cortisol content ↓ | ( | |
| 50 mg kg−1 of BW | (3) Heat tolerance, oxidative status and semen quality ↑ | ( | |
| 1,000 mg kg−1 of diet | (4) Hematological and antioxidative indicators ↑ | ( | |
| 10 mg kg−1 of BW | (5) Redox status, hormonal balance, total litter size, kindling rate, litter size at birth and litter weight at birth ↑ | ( | |
| Tannins | 10 g·kg−1 of diet | Body weight, feed intake, SOD, T-AOC and GSH-Px activities ↑, MDA and cortisol levels ↓ | ( |
| 5 or 10 g·kg−1 of diet | Growth performance, carcass and meat quality traits ↑, lipid peroxidation of meat ↓ | ( |
BW, body weight; DW, drinking water.
Arrow, ↑: increase, ↓: decrease.