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胃饥饿素可降低肝脏线粒体脂肪酸β氧化。

Ghrelin reduces hepatic mitochondrial fatty acid beta oxidation.

作者信息

Rigault C, Le Borgne F, Georges B, Demarquoy J

机构信息

INSERM, Faculty of Sciences Gabriel, Metabolic and Nutritional Biochemics (LBMN), University of Burgundy, Dijon, France.

出版信息

J Endocrinol Invest. 2007 Apr;30(4):RC4-8. doi: 10.1007/BF03346290.

Abstract

Ghrelin is a 28-amino-acid peptide secreted during starvation by gastric cells. Ghrelin physiologically induces food intake and seems to alter lipid and glucid metabolism in several tissues such as adipose tissue and liver. Liver has a key position in lipid metabolism as it allows the metabolic orientation of fatty acids between oxidation and esterification. We investigated the effects of peripheral ghrelin administration on 2 crucial parameters of fatty acid oxidation: the levocarnitine (L-carnitine)-dependent entry of the fatty acids in the mitochondria and the mitochondrial fatty acid oxidation. Ghrelin was either given to rats prior to the hepatocyte preparation and culture or used to treat hepatocytes prepared from control animals. Direct incubation of ghrelin to raw hepatocytes did not induce any change in the studied parameters. In hepatocytes prepared from 3 nmol ghrelin-treated rats, a 44% reduction of the mitochondrial fatty acid oxidation while no alteration of the L-carnitine-related parameters were observed. These results suggested (a) that ghrelin has no direct effect on liver, and (b) that when administrated to a whole organism, ghrelin may alter the lipid metabolism and the energy balance through a marked decrease in liver fatty acid oxidation.

摘要

胃饥饿素是一种由胃细胞在饥饿时分泌的含28个氨基酸的肽。胃饥饿素在生理上可诱导食物摄入,并且似乎会改变多个组织(如脂肪组织和肝脏)中的脂质和糖类代谢。肝脏在脂质代谢中具有关键地位,因为它决定了脂肪酸在氧化和酯化之间的代谢方向。我们研究了外周给予胃饥饿素对脂肪酸氧化的两个关键参数的影响:左旋肉碱(L-肉碱)依赖性脂肪酸进入线粒体的过程以及线粒体脂肪酸氧化。胃饥饿素要么在制备和培养肝细胞之前给予大鼠,要么用于处理从对照动物制备的肝细胞。将胃饥饿素直接与原代肝细胞一起孵育并未引起所研究参数的任何变化。在由3 nmol胃饥饿素处理的大鼠制备的肝细胞中,线粒体脂肪酸氧化减少了44%,而未观察到与L-肉碱相关的参数有任何改变。这些结果表明:(a)胃饥饿素对肝脏没有直接影响;(b)当给予整个生物体时,胃饥饿素可能通过显著降低肝脏脂肪酸氧化来改变脂质代谢和能量平衡。

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