Oiso Shigeru, Nobe Miyuki, Iwasaki Syuhei, Nii Wakana, Goto Natsumi, Seki Yukari, Nakajima Kensuke, Nakamura Kazuo, Kariyazono Hiroko
Graduate School of Pharmaceutical Sciences, Nagasaki International University.
J Oleo Sci. 2015;64(11):1185-92. doi: 10.5650/jos.ess15137.
Ghrelin is a growth hormone-releasing peptide that also displays orexigenic activity. Since serine-3 acylation with octanoylate (octanoylation) is essential for the orexigenic activity of ghrelin, suppression of octanoylation could lead to amelioration or prevention of obesity. To enable the exploration of inhibitors of octanoylated ghrelin production, we developed a cell-based assay system using AGS-GHRL8 cells, in which octanoylated ghrelin concentration increases in the presence of octanoic acid. Using this assay system, we investigated whether fatty acids contained in foods or oils, such as acetic acid, stearic acid, oleic acid, linoleic acid, and α-linolenic acid, have inhibitory effects on octanoylated ghrelin production. Acetic acid did not suppress the increase in octanoylated ghrelin production in AGS-GHRL8 cells, which was induced by the addition of octanoic acid. However, stearic acid, oleic acid, linoleic acid, and α-linolenic acid significantly suppressed octanoylated ghrelin production, with the effect of oleic acid being the strongest. Additionally, oleic acid decreased the serum concentration of octanoylated ghrelin in mice. The serum concentration of des-acyl ghrelin (without acyl modification) was also decreased, but the decrease was smaller than that of octanoylated ghrelin. Decreased octanoylated ghrelin production likely resulted from post-translational ghrelin processing, as there were no significant differences in gene expression in the stomach between oleic acid-treated mice and controls. These results suggest that oleic acid is a potential inhibitor of octanoylated ghrelin production and that our assay system is a valuable tool for screening compounds with suppressive effects on octanoylated ghrelin production.
胃饥饿素是一种生长激素释放肽,也具有促食欲活性。由于胃饥饿素的促食欲活性依赖于丝氨酸-3位的辛酰化修饰,抑制辛酰化修饰可能改善或预防肥胖。为了筛选胃饥饿素辛酰化修饰的抑制剂,我们构建了基于AGS-GHRL8细胞的检测系统,在该系统中,添加辛酸后胃饥饿素的辛酰化修饰水平会增加。利用该检测系统,我们研究了食品或油类中含有的脂肪酸,如乙酸、硬脂酸、油酸、亚油酸和α-亚麻酸,对胃饥饿素辛酰化修饰的抑制作用。乙酸不能抑制AGS-GHRL8细胞中由辛酸诱导的胃饥饿素辛酰化修饰水平的增加。然而,硬脂酸、油酸、亚油酸和α-亚麻酸均能显著抑制胃饥饿素的辛酰化修饰,其中油酸的抑制作用最强。此外,油酸可降低小鼠血清中胃饥饿素的辛酰化修饰水平。去酰基胃饥饿素(未进行酰基修饰)的血清水平也有所降低,但降低幅度小于胃饥饿素的辛酰化修饰水平。胃饥饿素辛酰化修饰水平的降低可能是由于其翻译后加工过程受到影响,因为油酸处理组小鼠与对照组小鼠胃组织中的基因表达没有显著差异。这些结果表明,油酸是胃饥饿素辛酰化修饰的潜在抑制剂,我们构建的检测系统是筛选抑制胃饥饿素辛酰化修饰化合物的有效工具。