Hostname: page-component-78c5997874-dh8gc Total loading time: 0 Render date: 2024-11-16T15:22:56.095Z Has data issue: false hasContentIssue false

Thymol supplementation effects on adrenocortical, immune and biochemical variables recovery in Japanese quail after exposure to chronic heat stress

Published online by Cambridge University Press:  09 July 2018

F. N. Nazar
Affiliation:
Instituto de Ciencia y Tecnología de los Alimentos (ICTA), Facultad de Ciencias Exactas, Físicas y Naturales, Universidad Nacional de Córdoba (UNC), Córdoba X5000JJC, Argentina Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Instituto de Investigaciones Biológicas y Tecnológicas (IIByT, CONICET-UNC), Córdoba X5000JJC, Argentina
E. A. Videla
Affiliation:
Instituto de Ciencia y Tecnología de los Alimentos (ICTA), Facultad de Ciencias Exactas, Físicas y Naturales, Universidad Nacional de Córdoba (UNC), Córdoba X5000JJC, Argentina Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Instituto de Investigaciones Biológicas y Tecnológicas (IIByT, CONICET-UNC), Córdoba X5000JJC, Argentina
R. H. Marin*
Affiliation:
Instituto de Ciencia y Tecnología de los Alimentos (ICTA), Facultad de Ciencias Exactas, Físicas y Naturales, Universidad Nacional de Córdoba (UNC), Córdoba X5000JJC, Argentina Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Instituto de Investigaciones Biológicas y Tecnológicas (IIByT, CONICET-UNC), Córdoba X5000JJC, Argentina
*
Get access

Abstract

Chronic heat stress (CHS) exposure negatively impairs avian’ immunoneuroendocrine interplay. Thymol has shown several bioactive properties including antioxidant, bactericidal, antifungal and gamma-aminobutyric acid modulator activities. Indeed, supplementation with thymol has been used with positive effects on poultry production and immune-related variables. This study evaluates whether a thymol dietary supplementation can be used as a new functional feed strategy to mitigate CHS deleterious effects on endocrine, biochemical and immune-related variables. Starting at 100 days of age, 24 fully adult Japanese quail were fed with a diet supplemented with thymol (≈80 mg/quail per day) and other 24 quail remained non-supplemented (control diet). Between 119 and 127 days of age, half of the quail within those groups were submitted to a CHS by increasing environmental temperature from 24°C to 34°C during the light phase and the other half remained at 24°C (non-stressed controls). A period of 3 days after CHS ended (during the recovery period), corticosterone, albumin, total proteins and globulins and glucose concentrations, inflammatory response, antibody production and heterophil to lymphocyte (H/L) ratio were assessed. No differences between groups were found in basal corticosterone concentrations. Total proteins, total globulins and glucose concentrations were found elevated in the previously CHS group compared with their control counterparts. Regardless of the previous CHS exposure, thymol supplementation increased albumin concentrations and inflammatory responses and decreased antibody titers. An interaction between thymol supplementation and prior CHS exposure was found on the H/L ratio. Quail previously exposed to CHS and supplemented with thymol showed similar H/L values than their control non-stressed counterparts, suggesting that thymol has a stress preventive effect on this variable. The present findings together with the already reported thymol bioactive properties, suggest that feed supplementation with this compound could be a useful strategy to help overcoming some of the CHS induced alterations.

Type
Research Article
Copyright
© The Animal Consortium 2018 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Footnotes

a

Share first authorship.

References

Adriaansen-Tennekes, R, Decuypere, E, Parmentier, HK and Savelkoul, HFJ 2009. Chicken lines selected for their primary antibody response to sheep red blood cells show differential hypothalamic-pituitary-adrenal axis responsiveness to mild stressors. Poultry Science 88, 18791882.Google Scholar
Azad, MAK, Kikusato, M, Maekawa, T, Shirakawa, H and Toyomizu, M 2010. Metabolic characteristics and oxidative damage to skeletal muscle in broiler chickens exposed to chronic heat stress. Comparative biochemistry and physiology. Part A, Molecular & integrative physiology 155, 401406.Google Scholar
Belhadj Slimen I, Najar T, Ghram A and Abdrrabba M 2016. Heat stress effects on livestock: Molecular, cellular and metabolic aspects, a review. Journal of Animal Physiology and Animal Nutrition 100, 401–412. Google Scholar
Calefi, AS, Quinteiro-Filho, WM, Ferreira, AJP and Palermo-Neto, J 2017. Neuroimmunomodulation and heat stress in poultry. World’s Poultry Science Journal 73, 493504.Google Scholar
Campo, JL and Dávila, SG 2002. Effect of photoperiod on heterophil to lymphocyte ratio and tonic immobility duration of chickens. Poultry Science 81, 16371639.Google Scholar
Casagrande, S, Pinxten, R, Zaid, E and Eens, M 2014. Carotenoids, birdsong and oxidative status: Administration of dietary lutein is associated with an increase in song rate and circulating antioxidants (albumin and cholesterol) and a decrease in oxidative damage. PLoS ONE 9, e115899.Google Scholar
Chauhan, AK, Jakhar, R, Paul, S and Kang, SC 2014. Potentiation of macrophage activity by thymol through augmenting phagocytosis. International Immunopharmacology 18, 340346.Google Scholar
Dai, SF, Gao, F, Zhang, WH, Song, SX, Xu, XL and Zhou, GH 2011. Effects of dietary glutamine and gamma-aminobutyric acid on performance, carcass characteristics and serum parameters in broilers under circular heat stress. Animal Feed Science and Technology 168, 5160.Google Scholar
Davison, F 2013. Avian Immunology, 2nd edition. Elsevier, London, UK.Google Scholar
Di Rienzo, JA, Casanoves, F, Balzarini, MG, Gonzalez, L, Tablada, M and Robledo, CW 2016. Infostat. In Statistics (ed. Grupo InfoStat), pp. 45–150. FCA, Universidad Nacional de Cordoba, Cordoba, Argentina.Google Scholar
Dorman, HJD and Deans, SG 2000. Antimicrobial agents from plants: antibacterial activity of plant volatile oils. Journal of Applied Microbiology 88, 308316.Google Scholar
Elenkov, IJ, Wilder, RL, Chrousos, GP and Vizi, ES 2000. The sympathetic nerve – an integrative interface between two supersystems: the brain and the immune system. Pharmacological reviews 52, 595638.Google Scholar
Ezzat Abd El-Hack, M, Alagawany, M, Ragab Farag, M, Tiwari, R, Karthik, K, Dhama, K, Zorriehzahra, J and Adel, M 2016. Beneficial impacts of thymol essential oil on health and production of animals, fish and poultry: a review. Journal of Essential Oil Research 28, 365382.Google Scholar
García, DA, Bujons, J, Vale, C and Suñol, C 2006. Allosteric positive interaction of thymol with the GABAA receptor in primary cultures of mouse cortical neurons. Neuropharmacology 50, 2535.Google Scholar
Gasparino, E, Voltolini, DM, Del Vesco, AP, Guimarães, SEF, do Nascimento, CS and de Oliveira Neto, AR 2013. IGF-I, GHR and UCP mRNA expression in the liver and muscle of high- and low-feed-efficiency laying Japanese quail at different environmental temperatures. Livestock Science 157, 339344.Google Scholar
Gross, WB and Siegel, HS 1983. Evaluation of the heterophil/lymphocyte ratio as a measure of stress in chickens. Avian diseases 27, 972979.Google Scholar
Hashemipour, H, Kermanshahi, H, Golian, A and Veldkamp, T 2013. Effect of thymol and carvacrol feed supplementation on performance, antioxidant enzyme activities, fatty acid composition, digestive enzyme activities, and immune response in broiler chickens. Poultry Science 92, 20592069.Google Scholar
Huss, D, Poynter, G and Lansford, R 2008. Japanese quail (Coturnix japonica) as a laboratory animal model. Lab animal 37, 513519.Google Scholar
Krause, EL, Ternes, W, Krause, EL and Ternes, W 1999. Bioavailability of the antioxidative thyme compounds thymol and p-cymene-2,3-diol in eggs. European Food Research Technology 209, 140144.Google Scholar
Lábaque, MC, Kembro, JM, Luna, A and Marin, RH 2013. Effects of thymol feed supplementation on female Japanese quail (Coturnix coturnix) behavioral fear response. Animal Feed Science and Technology 183, 6772.Google Scholar
Ma, X, Lin, Y, Zhang, H, Chen, W, Wang, S, Ruan, D and Jiang, Z 2014. Heat stress impairs the nutritional metabolism and reduces the productivity of egg-laying ducks. Animal Reproduction Science 145, 182190.Google Scholar
Mashaly, MM, Hendricks, GL, Kalama, MA, Gehad, AE, Abbas, AO and Patterson, PH 2004. Effect of heat stress on production parameters and immune responses of commercial laying hens. Poultry Science 83, 889894.Google Scholar
Nazar, FN, Barrios, BE, Kaiser, P, Marin, RH and Correa, SG 2015. Immune neuroendocrine phenotypes in Coturnix coturnix: do avian species show LEWIS/FISCHER-like profiles? PloS one 10, e0120712.Google Scholar
Nazar, FN, Videla, EA, Fernandez, ME, Labaque, MC and Marin, RH 2018. Insights into thermal stress in Japanese quail (Coturnix coturnix): dynamics of immunoendocrine and biochemical responses during and after chronic exposure. Stress 21, 257266.Google Scholar
Prieto, MT and Campo, JL 2010. Effect of heat and several additives related to stress levels on fluctuating asymmetry, heterophil: lymphocyte ratio, and tonic immobility duration in White Leghorn chicks. Poultry Science 89, 20712077.Google Scholar
Quinteiro-Filho, WM, Ribeiro, A, Ferraz-de-Paula, V, Pinheiro, ML, Sakai, M, , LRM, Ferreira, AJP and Palermo-Neto, J 2010. Heat stress impairs performance parameters, induces intestinal injury, and decreases macrophage activity in broiler chickens. Poultry Science 89, 19051914.Google Scholar
Renaudeau, D, Collin, A, Yahav, S, de Basilio, V, Gourdine, JL and Collier, RJ 2012. Adaptation to hot climate and strategies to alleviate heat stress in livestock production. Animal 6, 707728.Google Scholar
Romero, LM, Dickens, MJ and Cyr, NE 2009. The reactive scope model – a new model integrating homeostasis, allostasis, and stress. Hormones and Behavior 55, 375389.Google Scholar
Sahin, K, Onderci, M, Sahin, N, Gursu, MF, Khachik, F and Kucuk, O 2006. Effects of lycopene supplementation on antioxidant status, oxidative stress, performance and carcass characteristics in heat-stressed Japanese quail. Journal of Thermal Biology 31, 307312.Google Scholar
Sahin, K, Orhan, C, Tuzcu, Z, Tuzcu, M and Sahin, N 2012. Curcumin ameloriates heat stress via inhibition of oxidative stress and modulation of Nrf2/HO-1 pathway in quail. Food and Chemical Toxicology 50, 40354041.Google Scholar
Sánchez, ME, Turina, ADV, García, DA, Nolan, MV and Perillo, MA 2004. Surface activity of thymol: Implications for an eventual pharmacological activity. Colloids and Surfaces B: Biointerfaces 34, 7786.Google Scholar
Sandhu, MA, Mirza, FQ, Afzal, F and Mukhtar, N 2012. Effect of heat stress on cellular and humoral immunity and its cure with α-tocopherol in meat type birds. Livestock Science 148, 181188.Google Scholar
Scanes, CG 2014. Sturkie’s avian physiology, 6th edition. Elsevier, London, UK.Google Scholar
Scanes, CG 2016. Biology of stress in poultry with emphasis on glucocorticoids and the heterophil to lymphocyte ratio. Poultry Science 95, 22082215.Google Scholar
Vinkler, M, Bainova, H, Bainová, H and Albrecht, T 2010. Functional analysis of the skin-swelling response to phytohaemagglutinin. Functional Ecology 24, 10811086.Google Scholar
Zulkifli, I, Al-Aqil, A, Omar, AR, Sazili, AQ and Rajion, MA 2009. Crating and heat stress influence blood parameters and heat shock protein 70 expression in broiler chickens showing short or long tonic immobility reactions. Poultry Science 88, 471476.Google Scholar
Supplementary material: File

Nazar et al. supplementary material 1

Nazar et al. supplementary material

Download Nazar et al. supplementary material 1(File)
File 28.2 KB