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亮氨酸脑啡肽对脊髓镇痛的增强作用。

The potentiation of spinal analgesia by leucine enkephalin.

作者信息

Larson A A, Vaught J L, Takemori A E

出版信息

Eur J Pharmacol. 1980 Feb;61(4):381-3. doi: 10.1016/0014-2999(80)90077-1.

DOI:10.1016/0014-2999(80)90077-1
PMID:6892802
Abstract

In two strains of rats, intrathecal administration of morphine and met-enkephalin was found to produce a dose-dependent analgesic effect as measured by the tail-flick assay. Prior administration of leu-enkelphalin at a dose which had no analgesic effect was found to reduce significantly the analgesic ED50 of both morphine and met-enkephalin. Met-enkephalin pretreatment, at a similar sub-analgesic dose, was without effect. Thus, a differential interaction of the enkephalins with morphine is evident at spinal structures.

摘要

在两种品系的大鼠中,通过甩尾试验发现鞘内注射吗啡和甲硫氨酸脑啡肽可产生剂量依赖性镇痛作用。预先给予无镇痛作用剂量的亮氨酸脑啡肽可显著降低吗啡和甲硫氨酸脑啡肽的镇痛半数有效剂量(ED50)。以类似的亚镇痛剂量进行甲硫氨酸脑啡肽预处理则无此效果。因此,脑啡肽与吗啡在脊髓结构上存在明显的差异相互作用。

相似文献

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The potentiation of spinal analgesia by leucine enkephalin.亮氨酸脑啡肽对脊髓镇痛的增强作用。
Eur J Pharmacol. 1980 Feb;61(4):381-3. doi: 10.1016/0014-2999(80)90077-1.
2
Role of mu and delta receptors in the supraspinal and spinal analgesic effects of [D-Pen2, D-Pen5]enkephalin in the mouse.μ和δ受体在小鼠中[D-青霉胺2,D-青霉胺5]脑啡肽的脊髓上和脊髓镇痛作用中的作用
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Differential effects of leucine and methionine enkephalin on morphine-induced analgesia, acute tolerance and dependence.亮氨酸脑啡肽和蛋氨酸脑啡肽对吗啡诱导的镇痛、急性耐受及依赖性的不同作用。
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Opiate and peptide interaction: effect of enkephalins on morphine analgesia.阿片类药物与肽的相互作用:脑啡肽对吗啡镇痛的影响。
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Methionine-enkephalin antagonism and endorphin potentiation of narcotic-induced analgesia.蛋氨酸脑啡肽对麻醉诱导镇痛的拮抗作用及内啡肽对其的增强作用。
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Different mu receptor subtypes mediate spinal and supraspinal analgesia in mice.不同的μ受体亚型介导小鼠的脊髓和脊髓上镇痛作用。
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Analgesic activity of a novel bivalent opioid peptide compared to morphine via different routes of administration.一种新型二价阿片肽与吗啡经不同给药途径的镇痛活性比较。
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Analgesic effects of intraventricular morphine and enkephalins in nondependent and morphine-dependent rats.脑室内注射吗啡和脑啡肽对非成瘾和吗啡成瘾大鼠的镇痛作用。
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Eur J Pharmacol. 1984 Mar 16;99(1):15-21. doi: 10.1016/0014-2999(84)90427-8.

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