高良姜总黄酮对大鼠内脏高敏感性模型及镇痛作用研究

梁万年; 江涛; 陈艳芬; 冯毅凡; 楚博; 范华倩; 唐春萍

doi:10.11653/zgsyfjxzz2013070263

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高良姜总黄酮对大鼠内脏高敏感性模型及镇痛作用研究

更新时间：2024-01-04

- 高良姜总黄酮对大鼠内脏高敏感性模型及镇痛作用研究
- Effect of Total Flavonoids from on Visceral Hypersensitivity in Rat Model with Irritable Bowel Syndrome and Analgesic Effects
- 中国实验方剂学杂志 2013年19卷第7期页码：263-267
- 作者机构：
- 作者简介：
- 基金信息：
  
  广东省教育部产学研结合项目(2006D90504006);广东省自然科学基金项目(S2012040006768)
- DOI：10.11653/zgsyfjxzz2013070263
  中图分类号：
- 纸质出版日期：2013
- 稿件说明：
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梁万年, 江涛, 陈艳芬, 等. 高良姜总黄酮对大鼠内脏高敏感性模型及镇痛作用研究[J]. 中国实验方剂学杂志, 2013,19(7):263-267.

LIANG Wan-nian, JIANG Tao, CHEN Yan-fen, et al. Effect of Total Flavonoids from on Visceral Hypersensitivity in Rat Model with Irritable Bowel Syndrome and Analgesic Effects[J]. Chinese journal of experimental traditional medical formulae, 2013, 19(7): 263-267.
梁万年, 江涛, 陈艳芬, 等. 高良姜总黄酮对大鼠内脏高敏感性模型及镇痛作用研究[J]. 中国实验方剂学杂志, 2013,19(7):263-267. DOI： 10.11653/zgsyfjxzz2013070263.

LIANG Wan-nian, JIANG Tao, CHEN Yan-fen, et al. Effect of Total Flavonoids from on Visceral Hypersensitivity in Rat Model with Irritable Bowel Syndrome and Analgesic Effects[J]. Chinese journal of experimental traditional medical formulae, 2013, 19(7): 263-267. DOI： 10.11653/zgsyfjxzz2013070263.

摘要

目的: 研究高良姜总黄酮(GLJ)对乙酸诱导内脏高敏性肠易激综合征(IBS)模型大鼠的治疗作用及其镇痛作用。方法: 建立大鼠IBS模型

将实验动物随机分为模型组、匹维溴铵组(0.02 g·kg-1)、GLJ高、中、低剂量组(1

0.5

0.25 g·kg-1)

连续给药2 周后评估乙酸诱导IBS模型大鼠的腹部回缩反射(AWR)状态

观察GLJ对乙酸诱导IBS模型大鼠的治疗作用;采用热板法、乙酸扭体法、压尾法、甲醛法研究GLJ的镇痛作用。结果: GLJ能够有效降低乙酸诱导IBS模型大鼠内脏的敏感性(P<0.01或P<0.05);对热刺激、乙酸、甲醛所诱发的小鼠疼痛均有一定的抑制作用(P<0.01或P<0.05)。结论: GLJ对IBS模型大鼠有较好的治疗作用及镇痛作用。

Abstract

Objective: To study the therapeutic effect in visceral hypersensitivity rat model with irritable bowel syndrome (IBS) induced by acetic acid and analgesic effect of total flavonoids from Alpinia officinarum(GLJ) and supply experimental evidence to the therapy of irritable bowel syndrome. Method: IBS models in SD rats were established by acetic acid for 2 weeks

and then the rats were randomized into model group

pinaverium group

GLJ high dose group

GLJ middle dose group

and GLJ low dose group. After treatment for 2 weeks

the therapeutic effect of GLJ was assessed by observing the abdominal withdrawal reflex (AWR) condition. The analgesic effects of GLJ were observed in pain models of mice induced by hot plate

acetic acid

pressure and formalin. Result: GLJ could effectively reduce the sensitivity of visceral hypersensitivity rat model of IBS induced by acetic acid(P<0.01 or P<0.05) and had analgesic effect on the pain models of hot plate

acetic acid and formalin (P<0.01 or P<0.05). Conclusion: GLJ has better therapeutic effect on visceral hypersensitivity rat model of IBS and analgesic effect.

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