[Opioid receptors of the CNS: function, structure and distribution].

Ceskoslovenska fysiologie Pub Date : 2004-01-01
R Slamberová
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Abstract

Even though the alkaloids of opium, such as morphine and codeine, were isolated at the beginning of 19th century, the opioid receptors were not determined until 1970's. The discovery of endogenous opioid peptides, such as endorphins, enkephalins and dynorphins, has helped to differentiate between the specific opioid receptor subtypes, mu, delta and kappa, that are used up to now. Opioid receptors are distributed in the central nervous system unevenly. Each receptor subtype has its own specific and nonspecific agonists and antagonists. Opioides, as exogenous opioid receptor agonists, are drugs that are often used in medicine for their analgesic effects, but they are also some of the most heavily abused drugs in the world. Opioides may also induce long-term changes in the numbers and binding activities of opioid receptors. Some of our studies in fact demonstrate that prenatal morphine exposure can alter opioid receptors of adult rats. This may begin to provide insight into the sources of some of the morphological and behavioral changes in the progeny of mothers that received or abused opioides during pregnancy.

[中枢神经系统阿片受体:功能、结构和分布]。
虽然鸦片中的生物碱,如吗啡和可待因,在19世纪初就被分离出来,但阿片受体直到20世纪70年代才被确定。内源性阿片肽的发现,如内啡肽、脑啡肽和啡肽,有助于区分目前使用的特定阿片受体亚型mu、delta和kappa。阿片受体在中枢神经系统中分布不均匀。每种受体亚型都有自己的特异性和非特异性激动剂和拮抗剂。阿片类药物作为外源性阿片受体激动剂,因其镇痛作用在医学上经常被使用,但也是世界上滥用最严重的药物之一。阿片也可能引起阿片受体数量和结合活性的长期变化。事实上,我们的一些研究表明,产前吗啡暴露可以改变成年大鼠的阿片受体。这可能开始为在怀孕期间接受或滥用阿片类药物的母亲的后代的一些形态和行为变化的来源提供见解。
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