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脑室内注射吗啡肽和β-酪蛋白衍生吗啡样肽的镇痛活性:与吗啡(微)受体结合亲和力的相关性。

Analgesic activity of intracerebroventricular administration of morphiceptin and beta-casomorphins: correlation with the morphine (micro) receptor binding affinity.

作者信息

Chang K J, Cuatrecasas P, Wei E T, Chang J K

出版信息

Life Sci. 1982 May 3;30(18):1547-51. doi: 10.1016/0024-3205(82)90242-9.

Abstract

Analgesic activities of morphiceptin, beta-casomorphins, [D-Ala2, D-Leu5]enkephalin and Sandoz peptide, FK 33-824, were examined by intracerebroventricular administration in rats. Their relative potencies in vivo were compared with their receptors binding activities. The receptors binding affinities were determined from the competition curves against [3H]naloxone binding in the absence and presence of sodium ions for morphine (micro) receptors and against 125I-[D-A1A2, D-Leu]enkephalin binding for enkephalin (delta) receptors. A good correlation between analgesic activity and morphine (micro) receptor but not enkephalin (delta) receptor binding affinity was obtained. These data extend the hypothesis that morphine (micro) receptors mediate the major portion of the analgesic activity of opioids.

摘要

通过向大鼠脑室内给药,研究了吗啡肽、β-酪蛋白吗啡、[D-Ala2,D-Leu5]脑啡肽和山道士肽FK 33-824的镇痛活性。将它们在体内的相对效力与其受体结合活性进行了比较。通过在有无钠离子存在的情况下,针对吗啡(μ)受体与[3H]纳洛酮结合的竞争曲线,以及针对脑啡肽(δ)受体与125I-[D-A1A2,D-Leu]脑啡肽结合的竞争曲线,测定受体结合亲和力。结果发现镇痛活性与吗啡(μ)受体结合亲和力之间存在良好的相关性,但与脑啡肽(δ)受体结合亲和力之间不存在相关性。这些数据扩展了如下假说,即吗啡(μ)受体介导了阿片类药物镇痛活性的主要部分。

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