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首页> 外文期刊>The Indian journal of medical research >Antinociceptive effects of gabapentin & its mechanism of action in experimental animal studies
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Antinociceptive effects of gabapentin & its mechanism of action in experimental animal studies

机译:加巴喷丁的镇痛作用及其在动物实验研究中的作用机理

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Background & objectives: Several studies have shown the possible analgesic effects of gabapentin, widely used as an antiepileptic. Thus, clinical studies have been carried out especially for neuropathic syndroms. This study was undertaken to investigate experimentally whether gabapentin has analgesic effects in mice and rats. Methods: The mice were divided into 10 groups (n=7) with various treatments to assess central and peripheral antinociceptive activity of gabapentin. Hot plate, tail clip and tail flick tests were applied for the investigation of central antinociceptive activity and the writhing test was applied for the investigation of peripheral antinociceptive activity. In addition, we also evaluated the levels of PGE 2 and nNOS on perfused hippocampus slices of rats. Results: Gabapentin showed a peripheral antinociceptive effect at all doses and a central antinociceptive effect at 30mg/kg dose. While the L-NAME and cyproheptadine changed the central and peripheral effects of gabapentin, naloxone did not change these effects. In vitro studies showed that gabapentin significantly increased nNOS level. PGE 2 and nNOS were found to have an important role in the antinociceptive effects of gabapentin at all doses and its combinations with L-NAME, cyproheptadine, indomethacine, and naloxone. As expected, PGE 2 levels decreased in all groups, while nNOS levels increased, which is believed to be an adaptation mechanism. Interpretation & conclusions: Our findings indicate that arachidonate, nitrergic and serotonergic systems play an important role in the antinociceptive activity of gabapentin except for the opioidergic system. Additionally, this effect occured centrally and peripherally. These effects were also mediated by nNOS and PGE2.
机译:背景与目的:多项研究表明加巴喷丁(广泛用作抗癫痫药)可能具有镇痛作用。因此,已经进行了临床研究,特别是针对神经性综合征。进行该研究以实验研究加巴喷丁在小鼠和大鼠中是否具有镇痛作用。方法:将小鼠分为10组(n = 7),用不同的处理方法评估加巴喷丁的中枢和外周镇痛作用。用热板,尾夹和甩尾试验研究中枢抗伤害感受活性,并用扭体试验观察周围抗伤害感受活性。此外,我们还评估了大鼠海马灌注切片上PGE 2 和nNOS的水平。结果:加巴喷丁在所有剂量下均具有外周镇痛作用,在30mg / kg剂量下均具有中枢镇痛作用。尽管L-NAME和赛庚啶改变了加巴喷丁的中枢和外周作用,但纳洛酮并未改变这些作用。体外研究表明,加巴喷丁可显着提高nNOS水平。发现PGE 2 和nNOS在所有剂量的加巴喷丁及其与L-NAME,赛庚啶,吲哚美辛和纳洛酮的组合中均具有重要的镇痛作用。正如预期的那样,所有组中PGE 2 的水平均下降,而nNOS的水平则上升,这被认为是一种适应机制。解释与结论:我们的发现表明,除阿片类药物系统外,花生四烯酸,硝能和5-羟色胺系统在加巴喷丁的抗伤害感受活性中也起着重要作用。此外,这种影响发生在中央和外围。这些效应也由nNOS和PGE2介导。

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