Suppr超能文献

山香圆叶的植物化学成分分析及其降血压潜力

Phytochemical analysis and hypotensive potential of Teucrium stocksianum Boiss.

机构信息

Laboratory of Cardiovascular Research and Integrative Pharmacology, College of Pharmacy, University of Sargodha, Pakistan.

Laboratory of Cardiovascular Research and Integrative Pharmacology, College of Pharmacy, University of Sargodha, Pakistan / Punjab University College of Pharmacy, University of the Punjab, Lahore, Pakistan.

出版信息

Pak J Pharm Sci. 2020 Nov;33(6(Supplementary)):2707-2713.

Abstract

Teucrium stocksianum Boiss. is an aromatic perennial herb. It has long been used traditionally in the treatment of hypertension in northern areas of Pakistan. The aim of this study was to evaluate its folkloric claim as hypotensive plant, phytochemical analysis and to predict potential phytoconstituent through in-silico studies. Hypotensive effect was investigated in anesthetized normotensive Sprague-Dawley rats. Recording of chronotropic and inotropic effect of plant extract in isolated right atria was done using tissue organ bath technique. Further, phytochemical characterization was performed through LC-MS. Whereas docking studies were carried out against M2 mAchR and Ca Channel receptor. Dose dependent reduction in systolic, diastolic, mean arterial pressure and heart rate was observed. Pretreatment with atropine and amlodipine significantly (p<0.001) reduced the hypotensive and negative chronotropic and inotropic effect. Phytochemical studies revealed the presence of twenty active compounds including Luteolin, Sarmentosin epoxide and Quinic acid. Docking studies showed pronounced interactions of majority of these phytochemicals with M2 mAch receptor in agonistic way and Ca Channel receptor in antagonistic way. Results speculate that dose dependent hypotensive and bradycardia effect of Teucrium stocksianum are mediated through muscarinic pathway and Caantagonism and is also well predicted by in-silico studies.

摘要

穗花香薷(Teucrium stocksianum Boiss.)是一种芳香的多年生草本植物。长期以来,它一直被巴基斯坦北部地区用于治疗高血压。本研究旨在评估其作为降压植物的民间说法,进行植物化学分析,并通过计算机模拟研究预测潜在的植物成分。在麻醉的正常血压 Sprague-Dawley 大鼠中研究了降压作用。使用组织器官浴技术在分离的右心房中记录植物提取物的变时和变力作用。进一步通过 LC-MS 进行植物化学表征。而对接研究是针对 M2 mAchR 和 Ca 通道受体进行的。观察到剂量依赖性降低收缩压、舒张压、平均动脉压和心率。阿托品类和氨氯地平预处理显著(p<0.001)降低了降压和负变时和变力作用。植物化学研究表明存在二十种活性化合物,包括木犀草素、桑枝素环氧化物和奎尼酸。对接研究表明,这些植物化学物质中的大多数与 M2 mAch 受体以激动方式和 Ca 通道受体以拮抗方式表现出明显的相互作用。结果表明,穗花香薷的剂量依赖性降压和心动过缓作用是通过毒蕈碱途径和 Ca 拮抗作用介导的,计算机模拟研究也很好地预测了这一点。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验