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镇痛持续时间与阿片类药物药代动力学变量的关系。

Relationship of duration of analgesia to opioid pharmacokinetic variables.

作者信息

Levine J, Gordon N C, Poole T, Benowitz N

出版信息

Brain Res. 1983 Dec 19;289(1-2):391-4. doi: 10.1016/0006-8993(83)90049-5.

Abstract

That physiological effects are directly related to concentration at the site of action has been validated for only a few classes of drugs. For opiates, a direct correlation is known to exist between concentration and magnitude of analgesia, but has not been shown for duration of analgesia. These experiments in rats, using opiates whose elimination half-lives differ by a factor of 2 1/2, in a range of doses that produce 10-90% of maximal analgesic effect, show that duration is not dependent on dose or rate of elimination of opiate analgesics. The data suggest that analgesic duration is not determined by the pharmacokinetics of opiates at the receptors where these drugs act to elicit analgesia.

摘要

只有少数几类药物的生理效应已被证实与作用部位的浓度直接相关。对于阿片类药物,已知浓度与镇痛强度之间存在直接相关性,但镇痛持续时间与浓度的关系尚未得到证实。在这些大鼠实验中,使用消除半衰期相差2.5倍的阿片类药物,剂量范围为产生最大镇痛效果的10%-90%,结果表明,镇痛持续时间并不取决于阿片类镇痛药的剂量或消除速率。数据表明,镇痛持续时间并非由阿片类药物在引发镇痛作用的受体处的药代动力学所决定。

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