CGP7930: GABAB受体的正变构调节剂

C. L. Adams, A. J. Lawrence
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引用次数: 48

摘要

CGP7930(3-(3′,5′-二叔丁基-4′-羟基)苯基-2,2-二甲基丙醇)是GABAB受体的正变构调节剂。已经发现CGP7930在开放或高亲和力状态下调节GABAB受体,增加激动剂对受体的亲和力和激动剂刺激后的信号转导功效。GABAB异质亚基B2参与信号转导,但不参与配体结合,似乎是CGP7930和类似变构调节剂的作用位点。当在naïve动物中单独使用时,CGP7930在啮齿动物中作为抗焦虑药而没有其他明显的行为影响,并且还被证明可以减少啮齿动物对尼古丁,可卡因或酒精的自我给药,这表明通过阳性变构调节剂对GABAB受体的“微调”可能能够调节这些药物的滥用。巴氯芬,GABAB激动剂,目前被发现用于治疗成瘾和各种其他疾病,但这可能导致脱靶效应和耐受性。CGP7930与巴氯芬联合使用可以增强其效力,理论上可以将有害影响降至最低。CGP7930需要进一步的研究,但这种化合物和其他类似的化合物在临床环境中具有潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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CGP7930: A Positive Allosteric Modulator of the GABAB Receptor

CGP7930 (3-(3′,5′-Di-tert-butyl-4′-hydroxy)phenyl-2,2-dimethylpropanol) is a positive allosteric modulator of the metabotropic GABAB receptor. CGP7930 has been found to modulate the GABAB receptor in the open, or high affinity, state increasing agonist affinity for the receptor and signal transduction efficacy following agonist stimulation. The GABAB heteromeric subunit B2, involved in signal transduction but not ligand binding, seems to be the site of action of CGP7930 and similar allosteric modulators. When administered alone in naïve animals, CGP7930 acts as an anxiolytic in rodents without other overt behavioral effects and has also been demonstrated to reduce self-administration of nicotine, cocaine, or alcohol in rodents, suggesting that “fine tuning” of the GABAB receptor by positive allosteric modulators may be able to regulate abuse of these drugs. Baclofen, the GABAB agonist, is currently finding use in treating addiction and various other disorders, but this can result in off-target effects and tolerance. CGP7930 when co-administered with baclofen enhances its potency, which could in theory minimize deleterious effects. Further study of CGP7930 is required, but this compound, and others like it, holds potential in a clinical setting.

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