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小半夏汤对豚鼠离体肠管运动的影响
引用本文:林艳艳,聂克,卢燕,张勇.小半夏汤对豚鼠离体肠管运动的影响[J].中国实验方剂学杂志,2013,19(21):245-249.
作者姓名:林艳艳  聂克  卢燕  张勇
作者单位:山东中医药大学, 济南 250355;山东中医药大学, 济南 250355;山东中医药大学, 济南 250355;山东中医药大学, 济南 250355
基金项目:山东省高等学校科技计划项目(J09LF07);教育部留学回国人员科研启动基金(教外司留[2007]1108号)
摘    要:目的: 观察小半夏汤对豚鼠离体肠管收缩的影响,初步探讨其止吐的作用机制。 方法: 利用离体浴槽,观察小半夏汤(生药,下同) 0, 0.1, 0.25, 0.5, 1, 2.5, 5, 10, 20, 40 g·L-1]对豚鼠离体肠管自主收缩平均张力、振幅和频率的影响;以呕吐相关受体激动剂乙酰胆碱(Ach)、组胺(His)、五羟色胺(5-HT)、多巴胺(DA)为工具药,观察小半夏汤0, 2, 5, 10 g·L-1对各工具药致豚鼠离体肠管收缩平均张力、振幅、频率和最大张力的影响。 结果: 小半夏汤能剂量依赖性地抑制豚鼠离体肠管自主收缩,降低其收缩平均张力、振幅和频率(与空白对照组相比,P<0.05或P<0.01);先加Ach,His,5-HT再加小半夏汤2,5,10 g·L-1或小半夏汤2,5,10 g·L-1预处理均能明显抑制3种工具药所致肠管收缩,减少肠管收缩平均张力、振幅、频率和最大张力(分别与给小半夏汤前和不给小半夏汤相比,P<0.05或P<0.01);小半夏汤能够增大DA致肠管收缩平均张力、振幅和频率(分别与给小半夏汤前和不给小半夏汤相比,P<0.05或P<0.01),但对肠管收缩最小张力无明显影响。 结论: 小半夏汤能够抑制豚鼠离体肠管自主收缩,其作用机制可能是通过阻断M受体、H1受体、5-HT受体和D2受体等呕吐相关受体而介导,或直接作用于肠平滑肌而起作用,其止呕机制有待进一步研究。

关 键 词:小半夏汤  离体肠管  M受体  H1受体  5-HT受体  D2受体
收稿时间:2013/3/18 0:00:00

Effects of XiaoBanXia Decoction on Movement of Isolated Ileum in Guinea Pig
LIN Yan-yan,NIE Ke,LU Yan and ZHANG Yong.Effects of XiaoBanXia Decoction on Movement of Isolated Ileum in Guinea Pig[J].China Journal of Experimental Traditional Medical Formulae,2013,19(21):245-249.
Authors:LIN Yan-yan  NIE Ke  LU Yan and ZHANG Yong
Institution:Shandong University of Traditional Chinese Medicine, Ji'nan 250355, China;Shandong University of Traditional Chinese Medicine, Ji'nan 250355, China;Shandong University of Traditional Chinese Medicine, Ji'nan 250355, China;Shandong University of Traditional Chinese Medicine, Ji'nan 250355, China
Abstract:Objective: To observe the effect of Xiaobanxia decoction on the movement of isolated ileum in guinea pig and analyze the mechanism of anti-emetic effect of Xiaobanxia decoction(XBXD). Method: The effects of XBXD(0, 0.1, 0.25, 0.5, 1, 2.5, 5, 10, 20, 40 g·L-1) on ileum spontaneous contraction tension, amplitude and frequency were investigated in organ bath. Emesis-relating agonists acetylcholine (Ach), histamine (His), 5-hydroxytryptamine (5-HT), dopamine (DA) were used as tool drugs, the inhibitory effect of XBXD (0, 2, 5, 10 g·L-1) on contraction tension, amplitude and frequency of isolated ileum in guinea pig were observed. Result: XBXD could dose-dependently inhibit ileum spontaneous contractions, reducing the average tension, amplitude, frequency (P<0.05 or P<0.01 vs control). Ach, His and 5-HT could stimulate ileum contraction, enhance the tension, amplitude and frequency. All the three doses (10, 5, 2 g·L-1) of XBXD could suppress the ileum contraction stimulated by above three tool drugs, significantly reduced the contraction tension, amplitude and frequency (P<0.05 or P<0.01 vs before XBXD or XBXD 0 g·L-1). DA could inhibit the spontaneous contraction, the middle and small dose (5, 2 g·L-1) of XBXD could antagonize the inhibitory effect of DA, and enhance the contraction tension, amplitude and frequency (P<0.05 or P<0.01 vs before XBXD or XBXD 0 g·L-1). Conclusion: XBXD can inhibit spontaneous contractile activity of ileum in guinea pig, the mechanism may be related to blocking M, H1, 5-HT and D2receptors or directly suppressing ileum smooth muscle. The mechanism of anti-emetic effect of XBXD needs further study.
Keywords:Xiaobanxia decoction  isolated ileum  M receptor  H1 receptor  5-HT receptor  D2 receptor
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