首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Mutual Enhancement of Opioid and Adrenergic Receptors by Combinations of Opioids and Adrenergic Ligands Is Reflected in Molecular Complementarity of Ligands: Drug Development Possibilities
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Mutual Enhancement of Opioid and Adrenergic Receptors by Combinations of Opioids and Adrenergic Ligands Is Reflected in Molecular Complementarity of Ligands: Drug Development Possibilities

机译:阿片类药物和肾上腺素配体的组合对阿片样物质和肾上腺素受体的相互增强反映在配体的分子互补性中:药物开发的可能性

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摘要

Crosstalk between opioid and adrenergic receptors is well characterized and due to interactions between second messenger systems, formation of receptor heterodimers, and extracellular allosteric binding regions. Both classes of receptors bind both sets of ligands. We propose here that receptor crosstalk may be mirrored in ligand complementarity. We demonstrate that opioids bind to adrenergic compounds with micromolar affinities. Additionally, adrenergic compounds bind with micromolar affinities to extracellular loops of opioid receptors while opioids bind to extracellular loops of adrenergic receptors. Thus, each compound type can bind to the complementary receptor, enhancing the activity of the other compound type through an allosteric mechanism. Screening for ligand complementarity may permit the identification of other mutually-enhancing sets of compounds as well as the design of novel combination drugs or tethered compounds with improved duration and specificity of action.
机译:阿片受体与肾上腺素能受体之间的串扰已得到很好的表征,这是由于第二信使系统之间的相互作用,受体异二聚体的形成以及细胞外变构结合区的缘故。两种受体都结合两组配体。我们在这里提出受体串扰可以反映在配体的互补性中。我们证明,阿片类药物以微摩尔亲和力与肾上腺素化合物结合。另外,肾上腺素能化合物以微摩尔亲和力与阿片受体的细胞外环结合,而阿片类物质与肾上腺素能受体的细胞外环结合。因此,每种化合物类型均可与互补受体结合,通过变构机制增强另一种化合物的活性。配体互补性的筛选可以允许鉴定其他相互增强的化合物,以及设计新颖的联合药物或具有改善的作用时间和特异性的栓系化合物。

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