Suppr超能文献

在小鼠输精管中进行的阿片受体结合研究显示出耐受性但无依赖性。

Opiate receptor binding studies in the mouse vas deferens exhibiting tolerance without dependence.

作者信息

Rubini P, Schulz R, Wüster M, Herz A

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1982 May;319(2):142-6. doi: 10.1007/BF00503928.

Abstract

The apparent lack of dependence in highly opiate-tolerant isolated mouse vas deferens may conflict with unitary theories postulating a common biochemical mechanism for both phenomena. Therefore, attention focused on binding sites of the opiate receptors which in this tissue are located presynaptically. Binding studies conducted with homogenate of highly tolerant vasa deferentia revealed no significant different results as compared to naive tissues. Further studies examined the effect of guanine nucleotide on opiate receptor interaction. Apparently, mu-, delta- and kappa-opiate receptors in the mouse vas deferens proved resistant to the regulatory action of guanine nucleotide in naive and tolerant tissues. From these experiments, it is concluded that the binding characteristics of opiate receptors in the mouse vas deferens do not change with chronic activation. In addition, the lack of an effect of guanine nucleotide on opiate binding leads to the suggestion that binding sites are not coupled to adenylate cyclase in this tissue. Taken together, these findings draw the attention to the coupling mechanism of opiate receptors in the mouse vas deferens which may play a key role in the adaptational mechanisms following chronic opiate exposure.

摘要

在对阿片类药物高度耐受的离体小鼠输精管中,明显缺乏依赖性,这可能与假设这两种现象存在共同生化机制的单一理论相冲突。因此,注意力集中在阿片受体的结合位点上,在该组织中,这些受体位于突触前。与未处理的组织相比,用高度耐受的输精管匀浆进行的结合研究没有显示出显著不同的结果。进一步的研究考察了鸟嘌呤核苷酸对阿片受体相互作用的影响。显然,在未处理和耐受的组织中,小鼠输精管中的μ、δ和κ阿片受体对鸟嘌呤核苷酸的调节作用具有抗性。从这些实验可以得出结论,小鼠输精管中阿片受体的结合特性不会随着慢性激活而改变。此外,鸟嘌呤核苷酸对阿片结合缺乏影响,这表明在该组织中结合位点与腺苷酸环化酶不偶联。综上所述,这些发现引起了人们对小鼠输精管中阿片受体偶联机制的关注,该机制可能在慢性阿片暴露后的适应机制中起关键作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验