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不同类型的阿片类激动剂与μ、δ和κ阿片类结合位点的相互作用存在显著差异。

Different types of opiate agonists interact distinguishably with mu, delta and kappa opiate binding sites.

作者信息

Pfeiffer A, Herz A

出版信息

Life Sci. 1982;31(12-13):1355-8. doi: 10.1016/0024-3205(82)90380-0.

Abstract

The present studies were undertaken to evaluate whether different types of opiate agonists interact in a distinguishable manner with mu, delta and kappa opiate binding sites. Two approaches were employed: (a) the well known effects of metal ions on opiate agonist binding affinities of subsite selective ligands were studied at mu, delta and kappa sites in rat brain homogenates. Binding parameters were obtained by simultaneous computeranalysis of displacement curves using the prototypic ligands dihydromorphine (DHM), (D-Ala2, D-Leu5) enkephalin (DADL) and ethylketocyclazocine (EKC) of the mu, delta and kappa binding sites respectively. The results show that the effects of metal ions depend not only on the binding site, but also on the ligand under investigation. (b) The interaction of the delta agonist DADL with the mu agonist DHM was investigated at mu binding sites by characterizing the type of competition occurring between the two ligands. The interaction was of the noncompetitive type. It therefore appears that the various opiate agonists either interact preferentially with different parts of a larger receptor site area or bind to topographically distinct sites on a single receptor molecule which are coupled allosterically.

摘要

开展本研究是为了评估不同类型的阿片类激动剂是否以可区分的方式与μ、δ和κ阿片类结合位点相互作用。采用了两种方法:(a) 在大鼠脑匀浆的μ、δ和κ位点研究金属离子对亚位点选择性配体的阿片类激动剂结合亲和力的众所周知的影响。使用μ、δ和κ结合位点的原型配体二氢吗啡 (DHM)、(D-Ala2, D-Leu5) 脑啡肽 (DADL) 和乙基酮环唑新 (EKC),通过对置换曲线进行同步计算机分析获得结合参数。结果表明,金属离子的影响不仅取决于结合位点,还取决于所研究的配体。(b) 通过表征两种配体之间发生的竞争类型,在μ结合位点研究δ激动剂DADL与μ激动剂DHM的相互作用。这种相互作用是非竞争性的。因此,各种阿片类激动剂似乎要么优先与较大受体位点区域的不同部分相互作用,要么与单个受体分子上拓扑上不同的位点结合,这些位点通过变构相互偶联。

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