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阿片类镇痛药增加兔脑脊液中内源性阿片样活性能力的比较。

Comparison of the ability of opioid analgesics to increase endogenous opioid-like activity in the cerebrospinal fluid of rabbits.

作者信息

Kachur J F, Rosemond R, Welch S, Bowman E R, Martin B R, Brase D A, Dewey W L

出版信息

Life Sci. 1985 Dec 30;37(26):2549-55. doi: 10.1016/0024-3205(85)90613-7.

Abstract

We have previously demonstrated that the acute administration of morphine increases the level of endogenous substances, which have antinociceptive activity, in cerebrospinal fluid (CSF). The present study was conducted to determine whether other opioid analgesics exert a similar effect. CSF was withdrawn from the cisterna magna of anesthetized rabbits before and after s.c. injections of meperidine, pentazocine, levorphanol and methadone, and was bioassayed for opioid-like activity in the mouse tail-flick and phenylquinone writhing tests. The opioid-like activity of CSF taken 60 min after meperidine (50 mg/kg) was significantly increased in both bioassays, and the CSF level of meperidine was insufficient to account for this effect. Pentazocine (25-75 mg/kg) also significantly increased opioid-like activity in rabbit CSF, but the effects of methadone (5-10 mg/kg) and levorphanol (20 mg/kg) were less marked. Dextrorphan (20 mg/kg), diazepam (10 mg/kg) and pentobarbital (20 mg/kg) administration did not significantly increase opioid-like activity in CSF. It is concluded that the antinociceptive action of some opioid analgesics in rabbits may be mediated in part by the release of endogenous antinociceptive substances.

摘要

我们之前已经证明,急性给予吗啡会增加脑脊液(CSF)中具有抗伤害感受活性的内源性物质的水平。本研究旨在确定其他阿片类镇痛药是否也有类似作用。在皮下注射哌替啶、喷他佐辛、左啡诺和美沙酮之前及之后,从麻醉兔的枕大池抽取脑脊液,并在小鼠甩尾试验和苯醌扭体试验中对其进行阿片样活性生物测定。在两种生物测定中,哌替啶(50mg/kg)注射60分钟后采集的脑脊液的阿片样活性均显著增加,且脑脊液中哌替啶的水平不足以解释这种效应。喷他佐辛(25 - 75mg/kg)也显著增加了兔脑脊液中的阿片样活性,但美沙酮(5 - 10mg/kg)和左啡诺(20mg/kg)的作用不太明显。给予右啡烷(20mg/kg)、地西泮(10mg/kg)和戊巴比妥(20mg/kg)并未显著增加脑脊液中的阿片样活性。结论是,一些阿片类镇痛药在兔体内的抗伤害感受作用可能部分是由内源性抗伤害感受物质的释放介导的。

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