| Literature DB >> 30184101 |
Fengge Wang1, Shuxiong Chen1, Yanwen Jiang1, Yun Zhao1, Liting Sun1, Biaobiao Zheng1, Lu Chen1, Zhuo Liu1, Xue Zheng1, Kangle Yi2, Chunjin Li1, Xu Zhou1.
Abstract
Ammonia, produced mainly from the deamination of amino acids and glutamine, is one of the major toxic components in blood and tissues that may affect bovine health. However, the physiological and pathological roles of ammonia in the mammary glands are not understood clearly. In the present study, the bovine mammary epithelial cell line (MAC-T) was utilised as an in vitro model to determine the effects of ammonia on bovine mammary gland. We demonstrated that ammonia stimulated the production of intracellular reactive oxygen species, decreased mitochondrial membrane potential, interrupted intracellular calcium ion (Ca2+) homeostasis and induced cell apoptosis. Ammonia also significantly reduced cell viability and increased the proportion of apoptotic cells through enhancing the level of p53 phosphorylation and increasing the expressions of BAX, caspase 8, caspase 9, caspase 3. Interestingly, bumetanide, a specific Na+ K+ 2Cl--cotransporter inhibitor, dramatically abolished the damaging effects of ammonia on the cells. These data suggest that ammonia exposure induces apoptosis in bovine mammary epithelial cells via activation of the p53 pathway and the mitochondrial apoptotic pathway, and that these effects involved the Na+ K+ 2Cl--cotransporter.Entities:
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Year: 2018 PMID: 30184101 DOI: 10.1093/mutage/gey023
Source DB: PubMed Journal: Mutagenesis ISSN: 0267-8357 Impact factor: 3.000