首页> 美国卫生研究院文献>International Journal of Peptides >Interaction between Pirenzepine and Ninjinto a Traditional Japanese Herbal Medicine on the Plasma Gut-Regulated Peptide Levels in Humans
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Interaction between Pirenzepine and Ninjinto a Traditional Japanese Herbal Medicine on the Plasma Gut-Regulated Peptide Levels in Humans

机译:哌仑西平与Ninjinto(日本传统草药)之间的相互作用对人体血浆内脏调节肽水平的影响

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摘要

The Japanese herbal medicine (Kampo) Ninjinto has been used for the treatment of gastroenteritis, esogastritis, gastric atony, gastrectasis, vomiting, and anorexia. The pharmacological effects of Ninjinto on the gastrointestine are due to changes in the levels of gut-regulated peptide, such as motilin, somatostatin, calcitonin gene-related peptide (CGRP), substance P, and vasoactive intestinal polypeptide (VIP). The release of these peptides is controlled by acetylcholine (ACh) from the preganglionic fibers of the parasympathetic nerve. Thus, we examined the effects of the selective M1 muscarinic receptor antagonist pirenzepine on the elevation of Ninjinto-induced plasma the area under the plasma gut-regulated peptide concentration-time curve from 0 to 240 min (AUC0→240 min) in humans. Oral pretreatment with pirenzepine significantly reduced the Ninjinto-induced elevation of plasma motilin and substance P release (AUC0→240 min). Combined treatment with Ninjinto and pirenzepine significantly increased the release of plasma somatostatin (AUC0→240 min) compared with administration of Ninjinto alone or placebo. Ninjinto appeared to induce the release of substance P and motilin into plasma mainly through the activation of M1 muscarinic receptors, and pirenzepine may affect the pharmacologic action of Ninjinto by the elevation of plasma substance P, motilin, and somatostatin.
机译:日本草药(仁宝)Ninjinto已用于治疗肠胃炎,食管胃炎,胃无力,胃气胀,呕吐和厌食。 Ninjinto对胃肠道的药理作用是由于肠道调节肽(例如胃动蛋白,生长抑素,降钙素基因相关肽(CGRP),P物质和血管活性肠多肽(VIP))水平的变化所致。这些肽的释放是由副交感神经的神经节前纤维中的乙酰胆碱(ACh)控制的。因此,我们研究了选择性M1毒蕈碱受体拮抗剂pirenzepine对Ninjinto诱导的血浆升高的影响,该浓度是人体血浆肠调节肽浓度-时间曲线从0到240 min(AUC0→240 min)的面积。哌仑西平口服预处理可显着降低Ninjinto诱导的血浆胃动素升高和P物质释放(AUC0→240 min)。与单独使用Ninjinto或安慰剂相比,Ninjinto和pirenzepine的联合治疗显着增加了血浆生长抑素的释放(AUC0→240 min)。 Ninjinto似乎主要通过激活M1毒蕈碱受体来诱导P物质和胃动素释放到血浆中,并且哌仑西平可能通过升高P物质,胃动素和促生长素抑制素来影响Ninjinto的药理作用。

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