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| Effect of relative humidity at either acute or chronic moderate temperature on growth performance and droppings’ corticosterone metabolites of broilers |
ZHOU ying*, LI Xiu-mei*, ZHANG Min-hong, FENG Jing-hai |
State Key Laboratory of Animal Nutrition, Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing 100193, P.R.China |
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Abstract The present study aimed to investigate the effect of relative humidity (RH) at either acute or chronic moderate ambient temperature (Ta) on growth performance and droppings’ corticosterone metabolites of broilers. Two experiments were conducted: effect of RH (35, 60 or 85%) on average daily feed intake (ADFI) and droppings’ corticosterone metabolites at acute (1 d: 20–26 or 31–20°C, 26 or 31°C for 6 h d–1 at 10:00–16:00) moderate Ta (experiment 1) and effect of RH (35, 60 or 85%) on growth performance and droppings’ corticosterone metabolites at chronic (step-wisely increasing temperature by 3°C every 3 d from 20 to 32°C within 15 d: 20–23–26–29–32°C) moderate Ta (experiment 2). Droppings were collected at the 2, 4, 6, 8, and 22 h after Ta-RH controlled in experiment 1 and at the 2, 4, 6, and 22 h after Ta controlled to 32°C in experiment 2. The results showed that: 1) In experiment 1, 85% RH increased (P<0.05) the droppings’ corticosterone metabolites at the 2, 6, 8, and 22 h and 35% RH increased (P<0.05) it at the 2 and 22 h compared to the 60% RH. Moreover, 85% RH further increased (P<0.05) it compared to the 35% RH, however, no difference (P>0.05) was found in ADFI among the three RH groups at acute moderate 26°C; 35 and 85% RH increased (P<0.05) droppings’ corticosterone metabolites at the 2, 6, 8 and 22 h and decreased (P<0.05) ADFI compared to the 60% RH, moreover, 85% RH further increased (P<0.05) droppings’ corticosterone metabolites and further decreased (P<0.05) ADFI compared to the 35% RH at acute moderate 31°C; and the average of droppings’ corticosterone metabolites in the whole period had a negative correlation (P<0.02) with the ADFI. 2) In experiment 2, 85% RH increased (P<0.01) droppings’ corticosterone metabolites only at the 2 h and decreased (P<0.02) ADFI and average daily gain (ADG) compared to the 60% RH, no difference (P>0.05) in droppings’ corticosterone metabolites was found between the 35 and 60% RH, however, 35% RH decreased (P<0.01) ADG compared to the 60% RH, and the average of droppings’ corticosterone metabolites in the whole period also had a negative correlation (P<0.02) with ADFI and ADG. In conclusion, droppings’ corticosterone metabolites could be used as a RH stress index and low and high RH, especially high RH, reduced growth performance possibly through inducing RH stress at moderate temperature.
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Received: 19 January 2018
Accepted:
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| Fund: The authors gratefully thank our team for helping to complete the experiments and animal care. The present study was funded by the Key National Research and Development Program Project of China (2016YFD0500509), the National Science and Technology Support Plan Project of China (2012BAD39B02), and the Chinese Academy of Agricultural Science and Technology Innovation Team Project (ASTIP-IAS07). |
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Corresponding Authors:
Correspondence ZHANG Min-hong, E-mail: zmh66@126.com
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| About author: ZHOU Ying, E-mail: 1361841518@qq.com;
* These authors contributed equally to this study. |
Cite this article:
ZHOU ying, LI Xiu-mei, ZHANG Min-hong, FENG Jing-hai.
2019.
Effect of relative humidity at either acute or chronic moderate temperature on growth performance and droppings’ corticosterone metabolites of broilers. Journal of Integrative Agriculture, 18(1): 152-159.
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Adams R L, Rogler J C. 1968. The effects of dietary aspirin and humidity on the performance of light and heavy breed chicks. Poultry Science, 47, 1344–1348.
Biancani B, Dalt L D, Gallina G. 2017. Fecal cortisol radioimmunoassay to monitor adrenal gland activity in the bottlenose dolphin (Tursiops truncatus) under human care. Marine Mammal Science, 33, 1014–1034.
Bize P, Stocker A, Jenni-Eiermann S. 2010. Sudden weather deterioration but not brood size affects baseline corticosterone levels in nestling Alpine swifts. Hormones and Behavior, 58, 591–598.
Bradely E L, Holmes W N. 1971. The effects of hypophysectomy on adrenocortical function in the duck (Anas platyrhynchos). Journal of Endocrinology, 49, 437–457.
Breuner C W, Sprague R S, Patterson S H. 2013. Environment, behavior and physiology: Do birds use barometric pressure to predict storms? Journal of Experimental Biology, 216, 1982–1990.
Cao Y, Tveten A K, Stene A. 2017. Establishment of a non-invasive method for stress evaluation in farmed salmon based on direct fecal corticoid metabolites measurement. Fish & Shellfish Immunology, 66, 317–324.
Chen Y, Feng J H, Zhang M H. 2013. Effects of high temperature and dietary crude protein level on growth performance, nitrogen metabolism and nitrogen emission in broilers. Chinese Journal of Animal Nutrition, 25, 2254–2265. (in Chinese)
Cinque C, De Marco A, Mairesse J. 2017. Relocation stress induces short-term fecal cortisol increase in Tonkean macaques (Macaca tonkeana). Primates, 58, 315–321.
Cinque C, Zinni M, Zuena A R. 2018. Faecal corticosterone metabolites assessment in socially housed male and female Wistar rats. Endocrine Connections, 7, 250–257.
Cornale P, Macchi E, Renna M. 2016. Effect of cage type on fecal corticosterone concentration in buck rabbits during the reproductive cycle. Journal of Applied Animal Welfare Science, 19, 90–96.
Culbert J, Wells J W. 1975. Aspects of adrenal function in the domestic fowl. Journal of Endocrinology, 65, 363–376.
Danan D, Matar M A, Kaplan Z. 2018. Blunted basal corticosterone pulsatility predicts post-exposure susceptibility to PTSD phenotype in rats. Psychoneuroendocrinology, 87, 35–42.
Daniels-severs A, Goodwin A, Keiland L. 1973. Effect of chronic crowding and cold on the pituitary-adrenal system: Responsiveness to an acute stimulus during chronic stress. Pharmacology, 9, 348–356.
Dantzer B, Santicchia F, van Kesteren F. 2016. Measurement of fecal glucocorticoid metabolite levels in Eurasian red squirrels (Sciurus vulgaris): Effects of captivity, sex, reproductive condition, and season. Journal of Mammalogy, 97, 1385–1398.
Dehnhard M, Clauss M, Lechner-Doll M. 2001. Noninvasive monitoring of adrenocortical activity in roe deer (Capreolus capreolus) by measurement of fecal cortisol metabolites. General and Comparative Endocrinology, 123, 111–120.
Dehnhard M, Schreer A, Krone O. 2003. Measurement of plasma corticosterone and fecal glucocorticoid metabolites in the chicken (Gallus domesticus), the great cormorant (Phalacrocorax carbo), and the goshawk (Accipiter gentilis). General and Comparative Endocrinology, 131, 345–352.
Deyhim F, Teeter R G. 1991. Research note: Sodium and potassium chloride drinking water supplementation effects on acid-base balance and plasma corticosterone in broilers reared in thermoneutral and heat-distressed environments. Poultry Science, 70, 2551–2553.
Du R, Gu X H. 1997. Effects of environmental temperature and dietary energy levels on chicken plasma corticosterone level. Journal of Animal Husbandry and Veterinary, 28, 126–129. (in Chinese)
Fauteux D, Gauthier G, Berteaux D. 2017. Assessing stress in arctic lemmings: Fecal metabolite levels reflect plasma free corticosterone levels. Physiological and Biochemical Zoology, 90, 370–382.
Foley C, Papageorge S, Wasser S. 2001. Noninvasive stress and reproductive measures of social and ecological pressures in free-ranging African elephants. Conservation Biology, 15, 1134–1142.
Fraisse F, Cockrem D J F. 2006. Corticosterone and fear behaviour in white and brown caged laying hens. British Poultry Science, 47, 110–119.
Freeman B M. 1988. The domestic fowl in biomedical research: Physiological effects of the environment. World’s Poultry Science, 44, 41–60.
Frigerio D, Dittami J, Möstl E. 2004. Excreted corticosterone metabolites co-vary with ambient temperature and air pressure in male Greylag geese (Anser anser). General and Comparative Endocrinology, 137, 29–36.
Giloh M, Shinder D, Yahav S. 2012. Skin surface temperature of broiler chickens is correlated to body core temperature and is indicative of their thermoregulatory status. Poultry Science, 91, 175–188.
Gould N R, Siegel H S. 1985. Effects of corticotropin and heat on corticosteroid-binding capacity and serum corticosteroid in White Rock chickens. Poultry Science, 64, 144–148.
Goymann W, Stle M. 1999. Noninvasive fecal monitoring of glucocorticoids in spotted hyenas, Crocuta crocuta. General and Comparative Endocrinology, 114, 340–348.
Goymann W, Trappschuh M, Jensen W. 2006. Low ambient temperature increases food intake and dropping production, leading to incorrect estimates of hormone metabolite concentrations in European stonechats. Hormones and Behavior, 49, 644–653.
Herring G, Ackerman J T, Herzog M P. 2012. Mercury exposure may suppress baseline corticosterone levels in juvenile birds. Environmental Science & Technology, 46, 6339–6346.
Hester P Y, Smith S G, Wilson E K. 1981. The effect of prolonged heat stress on adrenal weight, cholesterol, and corticosterone in White Pekin ducks. Poultry Science, 60, 1583–1586.
Huber S, Palme R, Arnold W. 2003. Effects of season, sex, and sample collection on concentrations of fecal cortisol metabolites in red deer (Cervus elaphus). General and Comparative Endocrinology, 130, 48–54.
Hunt C, Hambly C. 2006. Faecal corticosterone concentrations indicate that separately housed male mice are not more stressed than group housed males. Physiology & Behavior, 87, 519–526.
Jaferi A, Nowak N, Bhatnagar S. 2003. Negative feedback functions in chronically stressed rats: Role of the posterior paraventricular thalamus. Physiology & Behavior, 78, 365–373.
Lacey B, Hamrita T K, Lacy M P. 2000. Assessment of poultry deep body temperature responses to ambient temperature and relative humidity using an on-line telemetry system. Transactions of the ASAE, 43, 717–721.
Lin H, Jiao H C, Buyse J. 2006. Strategies for preventing heat stress in poultry. Worlds Poultry Science, 62, 71–85.
Lin H, Zhang H F, Du R. 2005. Thermoregulation responses of broiler chickens to humidity at different ambient temperatures. II. Four weeks of age. Poultry Science, 84, 1173–1178.
Liu S J, Lu Q P, Zhang H F. 2010. Effects of high temperature and high humidity environment on growth performance, plasma cortisol concentration and immune function in growing pigs. Chinese Journal of Animal Nutrition, 22, 1214–1219. (in Chinese)
?opuckia R, Klichb D, ?cibiorc A, Go??biowskac D. 2018. Living in habitats affected by wind turbines may result in an increase in corticosterone levels in ground dwelling animals. Ecological Indicators, 84,165–171.
Mendonça-Furtado O, Izar P, Palme R. 2017. Validation of an enzyme immunoassay for measuring fecal cortisol metabolites of bearded (Sapajus libidinosus) and black (Sapajus nigritus) capuchins. International Journal of Primatology, 38, 1002–1016.
Milligan J L, Winn P N. 1964. The influence of temperature and humidity on broiler performance in environmental chambers. Poultry Science, 43, 817–824.
Misson B H. 1976. The effects of temperature and relative humidity on the thermoregulatory responses of grouped and isolated neonate chicks. Journal of Agricultural Science, 86, 34–43.
Möstl E, Palme R. 2002. Hormones as indicators of stress. Domestic animal Endocrinology, 23, 67–74.
NRC (National Research Council). 1994. Nutrient Requirements of Poultry. 9th ed. National Academic Press, Washington, D.C.
Pineda-Galindo E, Cerda-Molina A L, Mayagoitia-Novales L. 2017. Biological validations of fecal glucocorticoid, testosterone, and progesterone metabolite measurements in captive stumptail macaques (Macaca arctoides). International Journal of Primatology, 38, 985–1001.
Prince R P, Whitaker J H, Matterson L D. 1965. Response of chickens to temperature and relative humidity environment. Poultry Science, 44, 73–77.
Reece F N, Deaton J W, Kubena L F. 1972. Effects of high temperature and humidity on heat prostration of broiler chickens. Poultry Science, 51, 2021–2025.
Rettenbacher S E Möstl, Hackl R. 2004. Measurement of corticosterone metabolites in chicken droppings. British Poultry Science, 45, 704–711.
Romero L M, Reed J M, Wingfield J C. 2000. Effects of weather on corticosterone responses in wild free-living passerine birds. General and Comparative Endocrinology, 118, 113–122.
Sipari S, Ylönen H, Palme R. 2017. Excretion and measurement of corticosterone and testosterone metabolites in bank voles (Myodes glareolus). General and Comparative Endocrinology, 243, 39–50.
Siswanto H, Hau J, Carlsson H E. 2008. Corticosterone concentrations in blood and excretion in faeces after ACTH administration in male Sprague-Dawley rats. In Vivo, 22, 435–440.
De Souza J J, de Arruda A M, Domingos H G. 2013. Retracted article: Regional differences in the surface temperature of naked neck laying hens in a semi-arid environment. International Journal of Biometeorology, 57, 377–380.
Stevenson E T, Gese E M, Neuman-Lee L A. 2017. Levels of plasma and fecal glucocorticoid metabolites following an ACTH challenge in male and female coyotes (Canis latrans). Journal of Comparative Physiology (B), 188, 345–358.
Su H G, Zhang M H, Feng J H. 2014. Study of fecal corticosterone metabolites as a non-invasive index of thermal comfort in broiler chickens. Chinese Journal of Animal Nutrition, 26, 1563–1569. (in Chinese)
Teskey-Gerstl A, Bamberg E, Steineck T. 2000. Excretion of corticosteroids in urine and faeces of hares (Lepus europaeus). Journal of Comparative Physiology B, 170, 163–168.
Thanos P K, Cavigelli S A, Michaelides M. 2009. A non-invasive method for detecting the metabolic stress response in rodents: Characterization and disruption of the circadian corticosterone rhythm. Physiological Research/Academia Scientiarum Bohemoslovaca, 58, 219.
Touma C, Sachser N, Möstl E. 2003. Effects of sex and time of day on metabolism and excretion of corticosterone in urine and feces of mice. General and Comparative Endocrinology, 130, 267–278.
Turriani M, Bernabò N, Barboni B. 2016. Circadian rhythm and stress response in droppings of serinus canaria. Veterinary Medicine Internationalm, 2016, 1–9.
Webster K, Narayan E, De Vos N. 2017. Fecal glucocorticoid metabolite response of captive koalas (Phascolarctos cinereus) to visitor encounters. General and Comparative Endocrinology, 244, 157–163.
Williamson R A, Misson B H, Davison T F. 1985. The effect of exposure to 40 on the heat production and the serum concentrations of triiodothyronine, thyroxine, and corticosterone in immature domestic fowl. General and Comparative Endocrinology, 60, 178–186.
Winn P N, Godfrey E F. 1967. The effect of humidity on growth and feed conversion of broiler chickens. International Journal of Biometeorology, 11, 39–50.
Wolf T E, Bennett N C, Burroughs R. 2018. The impact of age-class and social context on fecal glucocorticoid metabolite levels in free-ranging male giraffes. General and Comparative Endocrinology, 255, 26–31.
Yahav S. 2000. Relative humidity at moderate ambient temperatures: Its effect on male broiler chickens and turkeys. British Poultry Science, 41, 94–100.
Yahav S, Goldfeld S, Plavnik I. 1995. Physiological responses of chickens and turkeys to relative humidity during exposure to high ambient temperature. Journal of Thermal Biology, 20, 245–253.
Yarnell K, Purcell R S, Walker S L. 2016. Fecal glucocorticoid analysis: Non-invasive adrenal monitoring in equids. Journal of Visualized Experiments, 110, 53479.
Zhou Y, Peng Q Q, Zhang M H. 2015. The influence of environmental relative humidity at intermittent moderate temperatures on body temperature, acid-base balance, performance of broilers. Chinese Journal of Animal Nutrition, 27, 3726–3735. (in Chinese)
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