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• W3200312014 endingPage "111079" @default.
• W3200312014 startingPage "111079" @default.
• W3200312014 abstract "Amylin is a 37-amino acid polypeptide that has been found to be involved in feeding regulation in some mammals, birds, and goldfish. We cloned amylin of Siberian sturgeon and detected its distribution pattern in 15 tissues. The expression levels in the periprandial period (pre-and post-feeding), the changes in the food intake, and the expression levels of related appetite factors after the intraperitoneal injection of amylin were detected. The expression of amylin was found to be the highest in the hypothalamus. Compared with 1 h pre-feeding, the expression levels of amylin in the hypothalamus and duodenum were increased significantly 1 h post-feeding. Compared with the control group (saline), intraperitoneal injection of 50 ng/g, 100 ng/g, and 200 ng/g of amylin significantly inhibited food intake at 1 h post injection, but not at 3 h and 6 h. The injection of 50 ng/g, 100 ng/g, and 200 ng/g amylin significantly inhibited the cumulative feed. After 1 h of 50 ng/g amylin injection, the levels of MC4R and somatostatin in the hypothalamus increased significantly, while the levels of amylin and NPY decreased significantly. The levels of CCK in the valvular intestine were increased significantly. Insulin in the duodenum was also increased significantly, but there was no significant change in ghrelin in the duodenum. These results show that amylin inhibits feeding in Siberian sturgeon by down-regulating the appetite-stimulating factor NPY and up-regulating the appetite-suppressing factors somatostatin, MC4R, CCK, and insulin. This study provides a theoretical basis for studying the feeding function and action mechanisms of amylin in Siberian sturgeon." @default.
• W3200312014 created "2021-09-27" @default.
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• W3200312014 date "2022-01-01" @default.
• W3200312014 modified "2023-09-22" @default.
• W3200312014 title "Identification, tissue distribution, and anorexigenic effect of amylin in Siberian sturgeon (Acipenser baeri)" @default.
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• W3200312014 doi "https://doi.org/10.1016/j.cbpa.2021.111079" @default.
• W3200312014 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/34534676" @default.
• W3200312014 hasPublicationYear "2022" @default.
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