阿克环素提取物(“病毒”)在离体大鼠主动脉环中的抗肾上腺素能作用

Nidya Lara, J. Rincón, M. Guerrero
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引用次数: 2

摘要

背景:治疗前列腺增生的症状是阿克环素(Kunth)的传统用途之一[N.V.]" Vira Vira ",合成科]在哥伦比亚。这种疾病的药物治疗主要依赖于α -1抗肾上腺素能药物,其机制尚未在以前使用波哥大进行研究。目的:研究大鼠离体主动脉环中大黄茎空部提取物的α -1抗肾上腺素能作用。方法:采用苯基肾上腺素(PE)或氯化钾刺激环,比较了枸杞子乙醇提取物、哌唑嗪(对照)和二甲基亚砜(对照)对环的影响。测定了乙醇提取物对PE加压效应的抑制能力(pD2′值)。为了量化bogotensis松弛剂的效力,将增加浓度的乙醇提取物(0.1µg/mL-0.1 mg/mL)累积加入到PE(0.1µM)或KCl (80 mM)预收缩的离体主动脉环中。为了探索一氧化氮(NO)可能的参与作用,将L-NAME(100µM)给予暴露于分离主动脉环中PE浓度累积增加的主动脉环(10µg/mL)。测定乙醇提取物的水溶液、丁醇和二氯甲烷组分(10µg/mL)。还进行了植物化学筛选。结果:普唑嗪和巴哥藤提取物对PE诱导的环收缩有明显的抑制作用,而对KCl诱导的环收缩的抑制作用较低。波哥藤乙醇提取物显示出高的降低PE压力反应的能力(pD´2:5.51),以及放松先前因PE而预收缩的环的总功效。对先前被KCl收缩的环的松弛作用和效力明显较低。L-NAME部分恢复了波哥大弧菌的抑制作用。水溶液馏分、丁醇馏分和二氯甲烷馏分的抑菌率低于乙醇馏分。植物化学筛选结果显示,黄酮类化合物和三萜代谢物显著存在。结论:上述结果提示波哥大藤具有平滑肌松弛作用,其机制与α -1抗肾上腺素能机制有关。这种反应部分依赖于NO,似乎是由于活性代谢物之间的相互作用,可能是类黄酮和/或萜类质的。
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ALPHA ANTIADRENERGIC EFFECT OF Achyrocline bogotensis EXTRACT (“Vira Vira”) IN ISOLATED RAT AORTIC RING
Background: The treatment of symptoms of prostatic hyperplasia is among the traditional uses of Achyrocline bogotensis (Kunth) [N.V. “Vira Vira”, Compositae] in Colombia. Pharmacological therapy for this disorder depends mainly on alpha-1 antiadrenergic agents, and the mechanism has not been studied previously using A. bogotensis. Objectives: To assess the alpha-1 antiadrenergic effect of the extract obtained from the aerial parts of A. bogotensis in isolated aortic rings from Wistar rats. Methods: The study compared the effects of the ethanol extract of A. bogotensis, prazosin (reference) and DMSO (control) in rings stimulated with phenylephrine (PE) or KCl. The capacity to reduce the PE pressor effect by the ethanol extract (pD2’ value) was determined. To quantify the A. bogotensis relaxant potency, increasing concentrations of the ethanol extract (0.1 µg/mL-0.1 mg/mL), were added cumulatively to isolated aortic rings pre-contracted with PE (0.1 µM) or KCl (80 mM). To explore the possible participation of nitric oxide (NO), L-NAME (100 µM) was administered to aortic rings exposed to cumulatively increasing concentrations of PE in isolated aortic rings in the presence of the extract (10 µg/mL). Aqueous, butanol and dichloromethane fractions (10 µg/mL) obtained from the ethanol extract were assayed. Phytochemical screening was also performed. Results: Prazosin and A. bogotensis extract notably reduced the contraction induced by PE whereas their inhibitory effect in rings contracted with KCl were lower. A. bogotensis ethanol extract showed a high capacity for reducing the PE pressor response (pD´2 : 5.51) as well as total efficacy for relaxing rings previously precontracted with PE. The relaxant efficacy and potency of A. bogotensis extract against rings previously contracted with KCl were notably lower. L-NAME partly reverted the inhibitory effect of A. bogotensis. Aqueous, butanol and dichloromethane fractions gave inhibitory responses lower than that obtained with the ethanol extract. Phytochemical screening of A. bogotensis extract revealed the significant presence of flavonoid and triterpene metabolites. Conclusions: These results suggest that A. bogotensis elicits a smooth muscle relaxant effect related to the alpha-1 antiadrenergic mechanism. This response is partially NO dependent and seems to be due to interactions among active metabolites likely to be of flavonoid and/or terpenoid nature.
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