Embryonic Thermal Manipulation Affects the Antioxidant Response to Post-Hatch Thermal Exposure in Broiler Chickens

Simple Summary The broiler chicken is one of the most important livestock species in the world, as it occupies a major role in the modern human diet. Due to uneven artificial selection pressures, the broiler has increased in size over the past few decades at the expense of its ability to withstand oxidative damage, the latter of which is often a byproduct of thermal stress. In order to attenuate the effects of heat stress, thermal manipulation (TM), which involves changes in incubation temperature at certain points of embryonic development, is increasingly being presented as a way in which to improve broiler thermotolerance. Therefore, the objective of this study was to investigate how TM might affect broiler response to post-hatch thermal stress in the context of the genes that help combat oxidative damage, namely the catalase, NADPH oxidase 4 (NOX4), and superoxide dismutase 2 (SOD2) genes. Expression of all three aforementioned genes differed significantly between TM and control chickens after exposure to cold and heat stress. Conclusively, TM may act as a viable mode of preventative treatment for broilers at risk of thermally induced oxidative stress. Abstract Thermal stress is a major source of oxidative damage in the broiler chicken (Gallus gallus domesticus) due to the latter's impaired metabolic function. While heat stress has been extensively studied in broilers, the effects of cold stress on broiler physiologic and oxidative function are still relatively unknown. The present study aimed to understand how thermal manipulation (TM) might affect a broiler's oxidative response to post-hatch thermal stress in terms of the mRNA expression of the catalase, NADPH oxidase 4 (NOX4), and superoxide dismutase 2 (SOD2) genes. During embryonic days 10 to 18, TM was carried out by raising the temperature to 39 degrees C at 65% relative humidity for 18 h/day. To induce heat stress, room temperature was raised from 21 to 35 degrees C during post-hatch days (PD) 28 to 35, while cold stress was induced during PD 32 to 37 by lowering the room temperature from 21 to 16 degrees C. At the end of the thermal stress periods, a number of chickens were euthanized to extract hepatic and splenic tissue from the heat-stressed group and cardiac, hepatic, muscular, and splenic tissue from the cold-stressed group. Catalase, NOX4, and SOD2 expression in the heart, liver, and spleen were decreased in TM chickens compared to controls after both cold and heat stress. In contrast, the expression levels of these genes in the breast muscles of the TM group were increased or not affected. Moreover, TM chicks possessed an increased body weight (BW) and decreased cloacal temperature (T-C) compared to controls on PD 37. In addition, TM led to increased BW and lower T-C after both cold and heat stress. Conclusively, our findings suggest that TM has a significant effect on the oxidative function of thermally stressed broilers.