首页> 美国卫生研究院文献>Evidence-based Complementary and Alternative Medicine : eCAM >The Traditional Japanese Medicine Rikkunshito Promotes Gastric Emptying via the Antagonistic Action of the 5-HT3 Receptor Pathway in Rats
【2h】

The Traditional Japanese Medicine Rikkunshito Promotes Gastric Emptying via the Antagonistic Action of the 5-HT3 Receptor Pathway in Rats

机译:传统中药Rikkunshito通过5-HT3受体通路的拮抗作用促进大鼠胃排空

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。
获取外文期刊封面目录资料

摘要

The traditional Japanese medicine rikkunshito ameliorates the nitric oxide-associated delay in gastric emptying. Whether rikkunshito affects gastric motility associated with 5-hydroxytryptamine (serotonin: 5-HT) receptors or dopamine receptors is unknown. We examined the effects of rikkunshito on the delay in gastric emptying induced by 5-HT or dopamine using the phenol red method in male Wistar rats. 5-HT (0.01–1.0 mg kg−1, i.p.) dose dependently delayed gastric emptying, similar to the effect of the 5-HT3 receptor agonist 1-(3-chlorophenyl) biguanide (0.01–1.0 mg kg−1, i.p.). Dopamine also dose dependently delayed gastric emptying. The 5-HT3 receptor antagonist ondansetron (0.04–4.0 mg kg−1) and rikkunshito (125–500 mg kg−1) significantly suppressed the delay in gastric emptying caused by 5-HT or 1-(3-chlorophenyl) biguanide. Hesperidin (the most active ingredient in rikkunshito) suppressed the 5-HT-induced delayed gastric emptying in a dose-dependent manner, the maximum effect of which was similar to that of ondansetron (0.4 mg kg−1). The improvement obtained by rikkunshito or ondansetron in delaying gastric emptying was completely blocked by pretreatment with atropine. Rikkunshito appears to improve delay in gastric emptying via the antagonistic action of the 5-HT3 receptor pathway.
机译:日本传统药物rikkunshito改善了与一氧化氮相关的胃排空延迟。 rikkunshito是否会影响与5-羟色胺(5-羟色胺:5-HT)受体或多巴胺受体相关的胃动力。我们用酚红法研究了雄性Wistar大鼠中rikkunshito对5-HT或多巴胺诱导的胃排空延迟的影响。 5-HT(0.01–1.0 mg kg −1 ,ip)剂量依赖性地延迟胃排空,类似于5-HT3受体激动剂1-(3-氯苯基)双胍(0.01–1.0)的作用mg kg -1 ,ip)。多巴胺还可以剂量依赖性地延迟胃排空。 5-HT3受体拮抗剂恩丹西酮(0.04–4.0 mg kg −1 )和rikkunshito(125–500 mg kg −1 )显着抑制了由以下原因引起的胃排空延迟5-HT或1-(3-氯苯基)双胍。橙皮苷(rikkunshito中最有效的成分)以剂量依赖性方式抑制5-HT诱导的胃排空延迟,其最大作用类似于恩丹西酮(0.4 mg kg -1 )。 rikkunshito或恩丹西酮在延迟胃排空方面的改善被阿托品预处理完全阻止。 Rikkunshito似乎通过5-HT3受体途径的拮抗作用改善了胃排空的延迟。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号