首页> 外文期刊>Journal of Pharmacy and Pharmacology >Nepetalactone: a new opioid analgesic from Nepeta caesarea Boiss (published errata appear in J Pharm Pharmacol 1998 Oct;50(10):1204 and 1998 Dec;50(12):following 1434)
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Nepetalactone: a new opioid analgesic from Nepeta caesarea Boiss (published errata appear in J Pharm Pharmacol 1998 Oct;50(10):1204 and 1998 Dec;50(12):following 1434)

机译:硝基甲酸酯:来自Nepeta Caesarea Boiss的新阿片类阿片镇痛药(发表的勘误表演于1998年10月1998年的J Pharm Pharmacolol; 50(10):1204和1998年DEC; 50(12):以下1434年)

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摘要

The essential oils of Nepeta species including Nepeta phyllochlamys P. H. Davis, N. nuda L. ssp. nuda, and N. caesarea Boiss. have been screened by use of the tail-flick and tail immersion (52.5 degrees C) methods. Of the species studied, only N. caesarea showed significant analgesic activity, besides marked sedation, which was also blocked by naloxone, indicating involvement of opioid receptors. Moreover, it was only active on mechanical, not thermal, algesic response which suggests specificity for specific opioid receptor subtypes, excluding mu-opioid receptors. Because 4a alpha,7alpha,7a alpha-nepetalactone is the main component of the essential oil of N. caesarea, and is present at very high levels (92-95%), it is concluded that 4a alpha,7alpha,7a alpha-nepetalactone is the active principle and has a specific opioid receptor subtype agonistic activity.
机译:近锥体种类的精油,包括奈特·菲尼霍克马狄尔州的P.H.戴维斯,N. Nuda L. SSP。 NUDA和N.Caesarea Boiss。 通过使用尾部轻弹和尾部浸泡(52.5℃)方法进行筛选。 除了标记的镇静之外,所研究的物种仅显示N.CaESarea显示出显着的镇痛活性,这也被纳洛酮阻断,表明阿片受体受体。 此外,它仅在机械,而不是热,艾尔氏响应上,这表明特异性阿片受体亚型的特异性,不包括MU-阿片受体。 因为4Aα,7Aα-硝基甲酸酯是N.Caesarea精油的主要成分,并且存在于非常高的水平(92-95%),得出结论,4Aα,7Alpha,7aα-硝基丙酮 是活性原理,具有特定的阿片类受体亚型激动活动。

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