Heat stress (HS), a harmful condition affecting animal production, reproduction, and welfare, occurs when an animal is exposed to temperatures that exceed its thermal comfort zone. Several nonspecific body responses involving neural, neuroendocrine, and immune systems are triggered to keep homeostasis in such conditions. These responses, primarily directed to cooling the body, also impact the hypothalamic-pituitary-gonadal axis, compromising the bovine female’s release of gonadotropins. Heat stress also promotes reactive oxygen species accumulation in ovarian cells, impairing protein folding and refolding, triggering antioxidant and DNA protection mechanisms. These mechanisms, directed to reduce cell metabolism and increase survival chances, are not always sufficient to protect the cell and result in apoptosis. Heat stress’s systemic and cellular consequences impact ovarian estradiol production, estrous behaviors, follicular development, oocytes and embryo competence, conception rates, pregnancy establishment and maintenance, and even the future reproductive efficiency of the progenies of cows exposed to HS during pregnancy. The combat of heat stress includes strategies to alleviate the effect of progressive global warming, management strategies to cool the animals, reduced metabolic heat, and methane production dietary approaches. The use of reproductive biotechs and genetic strategies to increase thermotolerant animals are also critical to overcoming the harmful effect of HS.
Ferreira, J., Mogollon Garcia, H.d., Pupulim, A., Rizzoto, G., Kastelic, J.p. (2021). Heat stress impact on bovine female reproduction. REVISTA BRASILEIRA DE REPRODUÇÃO ANIMAL, 45, 583-589 [10.21451/1809-3000.RBRA2021.078].
Heat stress impact on bovine female reproduction
Rizzoto G;
2021
Abstract
Heat stress (HS), a harmful condition affecting animal production, reproduction, and welfare, occurs when an animal is exposed to temperatures that exceed its thermal comfort zone. Several nonspecific body responses involving neural, neuroendocrine, and immune systems are triggered to keep homeostasis in such conditions. These responses, primarily directed to cooling the body, also impact the hypothalamic-pituitary-gonadal axis, compromising the bovine female’s release of gonadotropins. Heat stress also promotes reactive oxygen species accumulation in ovarian cells, impairing protein folding and refolding, triggering antioxidant and DNA protection mechanisms. These mechanisms, directed to reduce cell metabolism and increase survival chances, are not always sufficient to protect the cell and result in apoptosis. Heat stress’s systemic and cellular consequences impact ovarian estradiol production, estrous behaviors, follicular development, oocytes and embryo competence, conception rates, pregnancy establishment and maintenance, and even the future reproductive efficiency of the progenies of cows exposed to HS during pregnancy. The combat of heat stress includes strategies to alleviate the effect of progressive global warming, management strategies to cool the animals, reduced metabolic heat, and methane production dietary approaches. The use of reproductive biotechs and genetic strategies to increase thermotolerant animals are also critical to overcoming the harmful effect of HS.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.


