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4,5-环氧吗啡喃结构与细胞增殖的体外调节之间的关系

Relationship between 4,5-epoxymorphinan structure and in vitro modulation of cell proliferation.

作者信息

Hutchinson Mark R, Somogyi Andrew A

机构信息

Department of Clinical and Experimental Pharmacology, Level 5, Medical School North, University of Adelaide, Frome Road, Adelaide 5005, South Australia, Australia.

出版信息

Eur J Pharmacol. 2004 Jun 28;494(2-3):251-62. doi: 10.1016/j.ejphar.2004.04.049.

Abstract

Morphine belongs to the class of compounds known as 4,5-epoxymorphinans, which can alter immune function directly via receptors expressed by immune cells. However, the opioid characteristics of these receptors are not clear. Therefore, the aim of this study was to investigate the in vitro immunomodulatory effects of 24 structurally related 4,5-epoxymorphinans to allow further characterisation of the receptor that mediates the immunomodulation and to ascertain if there is any structure-effect relationship. The immunomodulation of 4,5-epoxymorphinans using isolated mouse splenocytes stimulated with concanavalin A resulted in five types of responses: an inverted bell shaped curve (oxycodone, inhibitory EC(50)=1.6 nM), an inhibitory concentration response curve (buprenorphine, inhibitory EC(50)=12.6 microM), an inverted bell-shaped curve with induction (morphine, induction EC(50)=1.7 microM), an induction concentration response curve (oxymorphone, induction EC(50)=20 nM), and the lack of any response (e.g. noroxycodone). Non-stereoselectivity, naloxone-insensitivity, naloxone-sensitivity and non-classical opioid rank order of effect were all observed. A structure-effect relationship was developed and significant evidence for non-classical opioid receptor function on immune cells was concluded.

摘要

吗啡属于被称为4,5-环氧吗啡烷的化合物类别,这类化合物可通过免疫细胞表达的受体直接改变免疫功能。然而,这些受体的阿片样物质特性尚不清楚。因此,本研究的目的是调查24种结构相关的4,5-环氧吗啡烷的体外免疫调节作用,以便进一步表征介导免疫调节的受体,并确定是否存在任何构效关系。使用伴刀豆球蛋白A刺激的分离小鼠脾细胞对4,5-环氧吗啡烷进行免疫调节产生了五种类型的反应:倒钟形曲线(羟考酮,抑制性半数有效浓度(EC50)=1.6 nM)、抑制性浓度反应曲线(丁丙诺啡,抑制性EC50=12.6 μM)、具有诱导作用的倒钟形曲线(吗啡,诱导性EC50=1.7 μM)、诱导性浓度反应曲线(羟吗啡酮,诱导性EC50=20 nM)以及无任何反应(例如去甲羟考酮)。观察到了非立体选择性、纳洛酮不敏感性、纳洛酮敏感性以及非经典阿片样物质效应的等级顺序。建立了构效关系,并得出了免疫细胞上非经典阿片样物质受体功能的重要证据。

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