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齐墩果酸降低小鼠血浆辛酰化胃饥饿素水平

Decreased Plasma Octanoylated Ghrelin Levels in Mice by Oleanolic Acid.

作者信息

Nakajima Kensuke, Maeda Narumi, Oiso Shigeru, Kariyazono Hiroko

机构信息

Department of Pharmacy, Faculty of Pharmaceutical Sciences, Nagasaki International University.

Graduate School of Pharmaceutical Sciences, Nagasaki International University.

出版信息

J Oleo Sci. 2019 Jan 1;68(1):103-109. doi: 10.5650/jos.ess18148. Epub 2018 Dec 12.

Abstract

Ghrelin is a stomach-derived peptide hormone with an appetite-stimulating effect. Octanoylation on the serine-3 residue of ghrelin by ghrelin O-acyl transferase (GOAT) is essential for its orexigenic effect. Mature octanoylated ghrelin is generated by the C-terminal cleavage of octanoylated proghrelin via prohormone convertases (furin, PC1/3, or PC2). We previously established an AGS-GHRL8 cell line that produces octanoylated ghrelin in the presence of octanoic acid, and found that oleanolic acid suppresses octanoylated ghrelin production in AGS-GHRL8 cells. Here, we investigated the effects of oleanolic acid in C57BL/6J mice fed a standard, high-fat, or high-glucose diet. Oral administration of oleanolic acid for seven days (20 or 40 mg/kg) reduced plasma octanoylated ghrelin levels and body weight gain in the standard diet-fed mice but not in other two diet-fed mice. There were no significant differences in ghrelin, GOAT, furin, PC1/3, and PC2 gene expression levels between the vehicle- and oleanolic acid-treated mice fed a standard diet. Octanoyl-CoA is a substrate for ghrelin octanoylation by GOAT. We found that oleanolic acid did not affect octanoyl-CoA production in vitro. Hence, the inhibitory effect of oleanolic acid on octanoylated ghrelin production may not be related to the decrease in octanoyl-CoA. The results of this study may provide valuable knowledge for the development of anti-obesity agents with an inhibitory effect on octanoylated ghrelin production.

摘要

胃饥饿素是一种由胃产生的具有刺激食欲作用的肽类激素。胃饥饿素O-酰基转移酶(GOAT)对胃饥饿素丝氨酸-3残基的辛酰化作用对其促食欲作用至关重要。成熟的辛酰化胃饥饿素是通过前激素转化酶(弗林蛋白酶、PC1/3或PC2)对辛酰化胃饥饿素原进行C端切割而产生的。我们之前建立了一种AGS-GHRL8细胞系,该细胞系在辛酸存在的情况下可产生辛酰化胃饥饿素,并发现齐墩果酸可抑制AGS-GHRL8细胞中辛酰化胃饥饿素的产生。在此,我们研究了齐墩果酸对喂食标准、高脂或高糖饮食的C57BL/6J小鼠的影响。对喂食标准饮食的小鼠口服齐墩果酸7天(20或40毫克/千克)可降低血浆辛酰化胃饥饿素水平和体重增加,但对另外两种饮食喂养的小鼠则无此作用。在喂食标准饮食的载体处理组和齐墩果酸处理组小鼠之间,胃饥饿素、GOAT、弗林蛋白酶、PC1/3和PC2基因表达水平没有显著差异。辛酰辅酶A是GOAT使胃饥饿素辛酰化的底物。我们发现齐墩果酸在体外不影响辛酰辅酶A的产生。因此,齐墩果酸对辛酰化胃饥饿素产生的抑制作用可能与辛酰辅酶A的减少无关。本研究结果可能为开发对辛酰化胃饥饿素产生具有抑制作用的抗肥胖药物提供有价值的知识。

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