探讨假马齿苋抗伤感受活性的可能作用机制。

Manju Bhaskar, A G Jagtap
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引用次数: 11

摘要

目的:早期的研究表明,假马齿苋(Bacopa monniera, BM),一种在印度草药中被描述为具有许多中枢神经作用的植物,被发现具有抗抑郁作用(甲醇提取物在20mg/kg和40mg/kg p.o)以及抗伤活性(水提取物(AE)在80mg /kg, 120mg /kg和160mg /kg p.o)。本研究旨在探讨假马齿苋(Bacopa monniera, AEBM)水提物(80mg /kg、120mg /kg和160mg /kg)的抗伤性作用机制。材料和方法:实验组小鼠和大鼠在严格的实验方案和条件下,分别给药AEBM,并与选择性α2受体阻滞剂育亨宾、选择性β1受体阻滞剂阿替洛尔、5 -羟色胺受体拮抗剂赛heptadine和非选择性阿片受体拮抗剂纳洛酮合用。结果:我们观察到AEBM在醋酸扭体试验中的抗伤感受作用可通过事先给予选择性育亨宾(1 mg/kg, i.p;AEBM处理组(14.50±2.26)和育亨宾预处理组(37.17±2.14),选择性β1阿替洛尔受体阻滞剂(1 mg/kg, i.p;AEBM处理组和育亨宾预处理组扭数分别为14.50±2.26和31.00±5.44)。在福尔马林试验中,AEBM减少舔舐时间的作用被先前用5 -羟色胺受体拮抗剂赛庚啶(1mg /kg, i.p;AEBM处理组和赛庚啶预处理组分别为47.33±2.25s和113.50±3.83s(ⅰ期0 ~ 5 min)和26.67±3.83s和88.17±7.27s(ⅱ期20 ~ 30 min)。AEBM患者甩尾潜伏期增加%可通过先前使用非选择性阿片受体拮抗剂纳洛酮(2mg/kg, i.p;aebm组和纳洛酮组分别为282.35和107.35)。结论:假马齿苋水提物的镇痛作用机制涉及内源性肾上腺素能、血清素能和阿片能系统。
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Exploring the possible mechanisms of action behind the antinociceptive activity of Bacopa monniera.

Aim: Earlier studies have demonstrated that Bacopa monniera (BM), a plant described in Ayurveda for many CNS actions was found to exhibit antidepressant (methanolic extract at 20mg/kg and 40mg/kg p.o.) as well as antinociceptive activity (aqueous extract (AE) at 80 mg/kg, 120 mg/kg and 160 mg/kg p.o.). The present study sought to explore the possible mechanisms of antinociceptive effects of aqueous extract of Bacopa monniera (AEBM) at 80 mg/kg, 120 mg/kg and 160 mg/kg given orally.

Materials and methods: AEBM was given singly as well as with selective α2 receptor blocker Yohimbine, selective β1 receptor blocker Atenolol, serotonin receptor antagonist Cyproheptadine and a non-selective opioid receptor antagonist naloxone in experimental groups of mice and rats under strict protocols and conditions.

Results: We observed that the antinociceptive effects of AEBM in the acetic acid writhing test was prevented by prior treatment with the selective Yohimbine (1 mg/kg, i.p; 14.50 ± 2.26 and 37.17 ± 2.14 writhes in the AEBM-treated and yohimbine pre-treated AEBM groups, respectively) and selective β1 Atenolol receptor blocker (1 mg/kg, i.p; 14.50 ± 2.26 and 31.00 ± 5.44 writhes in the AEBM-treated and yohimbine pre-treated AEBM groups, respectively). In the formalin test, the reduction in licking time with AEBM was found to be reversed by prior treatment with serotonin receptor antagonist Cyproheptadine (1 mg/kg, i.p; 47.33 ± 2.25s and 113.50 ± 3.83s (during phase I i.e. 0-5 min) and 26.67 ± 3.83s and 88.17 ± 7.27s (during phase II i.e. 20-30 min) in the AEBM-treated and Cyproheptadine pre-treated AEBM groups, respectively). The % increase in tail flick latency with AEBM was prevented by prior treatment with the non-selective opioid receptor antagonist naloxone (2mg/kg, i.p; 282.35 and 107.35 in the AEBM-treated and naloxone-treated groups, respectively).

Conclusions: Our results indicate, that the endogenous adrenergic, serotonergic and opioidergic systems are involved in the analgesic mechanism of action of the aqueous extract of Bacopa monniera.

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