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Effect of Eupatorium arnottianum on Gastrointestinal Tract

机译:紫茎泽兰对胃肠道的影响

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Aims: Eupatorium arnottianum Griseb is used in popular medicine for gastric pains. So, the aim of this study was to investigate the possible spasmolytic effects of ethanolic and dichloromethanic extracts of the plant using preclinical methods. Place and Duration of Study: Department of Pharmacology, School of Pharmacy and Biochemistry, Universidad de Buenos Aires, from September 2015 to May 2016. Methodology: The effects of Eupatorium arnottianum extracts and its isolated compounds were evaluated on isolated rat jejunum. Intestinal transit of charcoal meal after the administration of extract was determined and compared with the control group. Also, phytochemical study was performed. Results: The extracts inhibited non competitively the cumulative concentration–response curves induced by acetylcholine (1.10-9–1.10-5 M), with similar inhibition at the highest concentration (2 mg/mL: 66.2±8.7% of inhibition for ethanolic extract and 61.5±10.5% of inhibition for dichlorometanic extract). Also, both extracts non-competitively inhibited the curve response concentration induced by CaCl2 (1.10-4 -3. 10-1 M) and significantly reduced the maximal response in a concentration-dependent manner. Furthermore, E. arnottianum (62, 125 and 250 mg/Kg, per oral) significantly decreased the propulsion of the charcoal meal through the gastrointestinal tract (68% of inhibition for 250 mg/Kg ethanolic extract, 42% of inhibition for 125 mg/Kg dichlorometanic extract). Finally, nepetin, the major compound of the ethanolic extract and two major compounds of dichlorometanic extract, jaceosidin and nepetin, reduced the maximal response of the acethylcholine in isolated jejunum (30 μg/mL: 75% of inhibition for jaceosidin and 89% of inhibition for nepetin). Conclusion: The results of the present study could demonstrate that Eupatorium arnottianum plays a spasmolytic role in gastrointestinal motility by interfering in calcium influx. Also nepetin and jaceosidin, major components of ethanolic and dichlorometanic extracts could be responsible for these properties.
机译:目的:紫茎泽兰(Eupatorium arnottianum Griseb)被用于治疗胃痛的流行药物。因此,本研究的目的是使用临床前方法研究植物乙醇和二氯甲烷提取物的可能的解痉作用。研究的地点和持续时间:布宜诺斯艾利斯大学药理与生物化学学院药理学系,从2015年9月至2016年5月。方法:对分离出的大鼠空肠进行评价紫茎泽兰提取物及其分离的化合物的作用。确定给予提取物后木炭粉的肠运输并与对照组比较。另外,进行了植物化学研究。结果:提取物非竞争性地抑制了乙酰胆碱(1.10 -9 –1.10 -5 M)诱导的累积浓度-响应曲线,在最高浓度下具有相似的抑制作用(2 mg / mL:对乙醇提取物的抑制率为66.2±8.7%,对二氯metanic提取物的抑制率为61.5±10.5%。此外,两种提取物均非竞争性地抑制CaCl 2 (1.10 -4 -3。10 -1 M)诱导的曲线反应浓度,并且以浓度依赖的方式显着降低了最大响应。此外,麻疯草(E. arnottianum)(分别为62、125和250 mg / Kg,每次口服)显着降低了木炭粉通过胃肠道的推动力(250 mg / Kg乙醇提取物抑制作用为68%,125 mg / kg抑制作用为42% / Kg二氯metanic提取物)。最后,荆芥苷(乙醇提取物的主要化合物和二氯metanic提取物的两种主要化合物,水杨苷和荆芥苷)降低了分离空肠中乙酰胆碱的最大响应(30μg/ mL:水杨苷的抑制作用为75%,水杨酸抑制作用为89%对于荆芥)。结论:本研究的结果可以证明,紫茎泽兰通过干扰钙的流入而在肠胃蠕动中起痉挛作用。荆芥油和芥子油苷,乙醇和二氯metanic提取物的主要成分也可能负责这些属性。

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