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Flavonoids stimulate cholecystokinin peptide secretion from the enteroendocrine STC-1 cells

机译:黄酮类化合物刺激肠内分泌STC-1细胞分泌胆囊收缩素肽

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Animal experiments showed that flavonoids might have the potential for an anti-obesity effect by reducing weight and food intake. However, the exact mechanisms that could be involved in these proposed effects are still under investigation. The complex process of food intake is partially regulated by gastrointestinal hormones. Cholecystokinin (CCK) is the best known gastrointestinal hormone to induce satiety signal that plays a key role in food intake regulation. It is released from the endocrine cells (I cell) in response to the ingestion of nutrients into the small intestine. In this study, we investigated the possible effects of flavonoids (quercetin, kaempferol, apigenin, rutin and baicalein) on stimulation of CCK release in vitro using enteroendocrine STC-1 cells. In comparison with the control, quercetin, kaempferol and apigenin resulted in a significant increase in CCK secretion with quercetin showing the highest activity. On the other hand, no significant effect was seen by rutin and baicalein. To our knowledge, this is the first report to study the stimulation of CCK peptide hormone secretion from STC-1 cells by quercetin and kaempferol, rutin, apigenin and baicalein. Based on the cell-based results in this work, it can be suggested that the reported activity of flavonoids against food intake and weight could be mediated by stimulation of CCK signal which in turn is responsible for food intake reduction, but future animal and human studies are needed to confirm this conclusion at organism level. (C) 2016 Elsevier B.V. All rights reserved.
机译:动物实验表明,类黄酮可能通过减轻体重和食物摄入而具有抗肥胖作用。但是,可能涉及这些拟议效果的确切机制仍在研究中。食物摄入的复杂过程部分受到胃肠激素的调节。胆囊收缩素(CCK)是引起饱腹感信号的最著名的胃肠激素,其在食物摄入调节中起关键作用。响应于营养物质向小肠的摄入,它从内分泌细胞(I细胞)释放。在这项研究中,我们研究了类黄酮(槲皮素,山奈酚,芹菜素,芦丁和黄ical素)对肠内分泌STC-1细胞体外刺激CCK释放的可能作用。与对照相比,槲皮素,山奈酚和芹菜素导致CCK分泌显着增加,其中槲皮素显示出最高的活性。另一方面,芦丁和黄ical素未见明显作用。据我们所知,这是第一个研究槲皮素和山emp酚,芦丁,芹菜素和黄ical苷刺激STC-1细胞分泌CCK肽激素的报告。基于这项工作中基于细胞的结果,可以表明,所报道的黄酮类化合物对食物摄入和体重的活性可以通过刺激CCK信号来介导,而CCK信号又可以减少食物的摄入,但是未来的动物和人类研究需要在生物体水平上确认这一结论。 (C)2016 Elsevier B.V.保留所有权利。

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