UMRCNRS7213, Laboratory of Biophotonics and Pharmacology, Faculty of Pharmacy, University of Strasbourg, Illkirch, France; Faculty of Pharmacy, The University of Lahore, Pakistan.
Dr. Panjwani Center for Molecular Medicine and Drugs Research, International Center for Chemical and Biological Sciences, University of Karachi 75270, Pakistan.
Phytomedicine. 2019 Feb;53:163-170. doi: 10.1016/j.phymed.2018.09.020. Epub 2018 Sep 5.
Zanthoxylum armatum DC (Z. armatum), belonging to Rutaceae family, has been traditionally used for the treatment of various diseases such as hypertension, abdominal pain, headache, fever, high altitude sickness, diarrhea, dysentery, and as a tonic, condiment, and an anthelmintic treatment.
The present study aims to evaluate the vasorelaxant effect of a methanolic extract of the fruits of Z. armatum, isolate the active components and characterize the underlying mechanism.
A methanolic extract of fruits of Z. armatum was prepared and its vasorelaxant effect was studied using porcine coronary artery rings. Thereafter, the methanolic extract was analyzed, and a major compound was isolated and its structure elucidated (tambulin). Different pharmacological tools were used to characterize the vasorelaxant effect of tambulin.
The methanolic extract and the isolated tambulin caused similar endothelium-independent relaxations of porcine coronary artery rings with and without endothelium indicating a direct relaxing effect at the vascular smooth muscle. Tambulin did not affect the relaxation curves to the endothelium-dependent vasodilators, bradykinin and the calcium ionophore A23187 in rings with endothelium. Tambulin (1 µM) slightly but significantly shifted leftwards the concentration-relaxation curve to the endothelium-independent vasodilators, sodium nitroprusside (SNP), forskolin (FC) and isoproterenol but not those to soluble guanylyl cyclase activators (YC-1 and BAY 41-2272) and K channel openers (levcromakalim and 1-EBIO). Pretreatment with tambulin inhibited, in a concentration-dependent manner, contractions to KCl, serotonin (5-HT), CaCl and U46619 in coronary artery rings without endothelium. Both the protein kinase A (H-89, 10 µM) and the protein kinase G (Rp-8-br-cyclic GMPS, 30 µM) inhibitors significantly reduced relaxations to tambulin in coronary artery rings without endothelium.
The present findings indicate that tambulin isolated from Z. armatum (fruits) is a major active principle inducing vasorelaxation through a direct effect at the vascular smooth muscle and involving both the cyclic AMP and/or cyclic GMP relaxing pathways.
花椒(Zanthoxylum armatum DC),属于芸香科,传统上用于治疗高血压、腹痛、头痛、发热、高原病、腹泻、痢疾等各种疾病,也可用作补品、调味料和驱虫剂。
本研究旨在评估花椒果实甲醇提取物的血管舒张作用,分离活性成分并探讨其潜在机制。
制备花椒果实甲醇提取物,研究其对猪冠状动脉环的血管舒张作用。然后对甲醇提取物进行分析,分离出主要化合物并对其结构进行鉴定(花椒毒素)。使用不同的药理学工具来表征花椒毒素的血管舒张作用。
甲醇提取物和分离得到的花椒毒素均引起具有和不具有内皮的猪冠状动脉环相似的内皮非依赖性舒张,表明其对血管平滑肌有直接的舒张作用。花椒毒素不影响具有内皮的血管环中内皮依赖性血管舒张剂缓激肽和钙离子载体 A23187 的舒张曲线。花椒毒素(1 μM)轻微但显著地向左移动了内皮非依赖性血管舒张剂硝普钠(SNP)、福斯高林(FC)和异丙肾上腺素的浓度-舒张曲线,但不影响可溶性鸟苷酸环化酶激活剂(YC-1 和 BAY 41-2272)和 K 通道开放剂(levcromakalim 和 1-EBIO)的曲线。花椒毒素预处理以浓度依赖性方式抑制了无内皮的冠状动脉环中对 KCl、5-羟色胺(5-HT)、CaCl 和 U46619 的收缩反应。蛋白激酶 A(H-89,10 μM)和蛋白激酶 G(Rp-8-br-cyclic GMPS,30 μM)抑制剂均显著降低了无内皮冠状动脉环中花椒毒素引起的舒张反应。
本研究结果表明,从花椒(果实)中分离得到的花椒毒素是一种主要的活性成分,通过直接作用于血管平滑肌诱导血管舒张,涉及环 AMP 和/或环 GMP 舒张途径。