Antagonistic effects of nano-selenium on broilers hepatic injury induced by Cr(VI) poisoning in AMPK pathway
Cr (chromium, with common valence states of III and VI) is one of the common broiler feed additives. Liver injury and metabolic disorders could be caused by Cr (VI) (hexavalent chromium) poisoning in broilers. Oxidative damage and metabolic disorders of organisms caused by heavy metals could be anta...
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Veröffentlicht in: | Environmental science and pollution research international 2020-11, Vol.27 (33), p.41585-41595 |
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Sprache: | eng |
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Zusammenfassung: | Cr (chromium, with common valence states of III and VI) is one of the common broiler feed additives. Liver injury and metabolic disorders could be caused by Cr
(VI)
(hexavalent chromium) poisoning in broilers. Oxidative damage and metabolic disorders of organisms caused by heavy metals could be antagonized by nano-Se (nano-selenium). Nano-Se was chosen to study the antagonism of Cr
(VI)
poisoning in broilers. AMPK (Adenosine 5
,
-monophosphate-activated protein kinase) is known as a “cell energy regulator” and plays a key regulatory role in carbohydrate and lipid metabolism. AMPK pathway and
ACACA
/
CPT1A
two genes were selected to study the prevention and treatment of nano-Se on Cr
(VI)
poisoning in broilers and its molecular mechanism. For this purpose, 180 1-day-old AA (Arbor Acres) broilers were selected and randomly divided into 6 groups (
n
= 30) for further testing. After feeding as planned for 35 days, the livers of such broilers were taken for further examination including histopathological examination, differential gene expression analysis, and further validation on both mRNA and protein levels using related techniques like RT-qPCR, western blot, and immunohistochemistry (IHC). The histopathological examination suggested that the liver cells of the Cr
(VI)
poisoning group were more severely injured than the nano-Se addition group. RT-qPCR results showed that the relative expression of
ACACA
gene in the Cr
(VI)
poisoning group was significantly increased (
P
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ISSN: | 0944-1344 1614-7499 |
DOI: | 10.1007/s11356-020-08501-0 |