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葡萄籽酚类物质的亚慢性治疗抑制了胃饥饿素的产生,尽管苦味黄酮醇会在短期内刺激胃饥饿素的分泌。

Subchronic treatment with grape-seed phenolics inhibits ghrelin production despite a short-term stimulation of ghrelin secretion produced by bitter-sensing flavanols.

作者信息

Serrano Joan, Casanova-Martí Àngela, Depoortere Inge, Blay Maria Teresa, Terra Ximena, Pinent Montserrat, Ardévol Anna

机构信息

MoBioFood Research Group, Departament de Bioquímica i Biotecnologia, Universitat Rovira i Virgili, Tarragona, Spain.

Gut Peptide Research Lab, Translational Research Center for Gastrointestinal Disorders, KU Leuven, Leuven, Belgium.

出版信息

Mol Nutr Food Res. 2016 Dec;60(12):2554-2564. doi: 10.1002/mnfr.201600242. Epub 2016 Sep 26.

DOI:10.1002/mnfr.201600242
PMID:27417519
Abstract

SCOPE

Grape-seed phenolic compounds have recently been described as satiating agents in rats when administered as a whole phenolic extract (GSPE). This satiating effect may involve the release of satiating gut hormones such as GLP-1, although a short-term increase in the orexigenic hormone ghrelin was also reported. In this study, we investigated the short- and long-term effects of GSPE in rats, focusing on the role of the main grape-seed phenolics in ghrelin secretion.

METHODS AND RESULTS

GSPE produced a short-term increase in plasma ghrelin in rats after an acute treatment. A mouse ghrelinoma cell line was used to test the effects of the main pure grape-seed phenolic compounds on ghrelin release. Monomeric flavanols stimulated ghrelin secretion by activating bitter taste receptors. In contrast, gallic acid (GA) and oligomeric flavanols inhibited ghrelin release. The ghrelin-inhibiting effects of GA were confirmed in rats and in rat duodenal segments. One day after the last dose of a subchronic treatment, GSPE decreased plasma ghrelin in rats, ghrelin secretion in intestinal segments, and ghrelin mRNA expression in stomach.

CONCLUSION

The sustained satiating effects of GSPE are related to a long-term decrease in ghrelin expression. GA and oligomeric flavanols play a ghrelin-inhibiting role in this process.

摘要

范围

葡萄籽酚类化合物最近被描述为以总酚提取物(GSPE)形式给药时对大鼠具有饱腹感的物质。这种饱腹感作用可能涉及释放诸如胰高血糖素样肽-1(GLP-1)等饱腹感肠道激素,不过也有报道称促食欲激素胃饥饿素会出现短期增加。在本研究中,我们研究了GSPE对大鼠的短期和长期影响,重点关注主要葡萄籽酚类物质在胃饥饿素分泌中的作用。

方法与结果

急性处理后,GSPE使大鼠血浆胃饥饿素出现短期增加。使用小鼠胃饥饿素瘤细胞系来测试主要的纯葡萄籽酚类化合物对胃饥饿素释放的影响。单体黄烷醇通过激活苦味受体刺激胃饥饿素分泌。相比之下,没食子酸(GA)和低聚黄烷醇抑制胃饥饿素释放。GA对胃饥饿素的抑制作用在大鼠和大鼠十二指肠段得到证实。亚慢性处理的最后一剂给药一天后,GSPE降低了大鼠血浆胃饥饿素水平、肠段胃饥饿素分泌以及胃中胃饥饿素mRNA表达。

结论

GSPE持续的饱腹感作用与胃饥饿素表达的长期降低有关。GA和低聚黄烷醇在此过程中发挥胃饥饿素抑制作用。

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