Neuroscience Institute, Section of Cagliari, National Research Council of Italy, I-09042, Monserrato (CA), Italy.
Alcohol Alcohol. 2024 Mar 16;59(3). doi: 10.1093/alcalc/agae018.
Positive allosteric modulators (PAMs) of the GABAB receptor constitute a new class of GABAB-receptor ligands. GABAB PAMs reproduce several pharmacological effects of the orthosteric GABAB receptor agonist, baclofen, although displaying a better safety profile.
This paper reviews the reducing or, frequently, even suppressing effects of all GABAB PAMs tested to date on multiple alcohol-related behaviours in laboratory rodents exposed to validated experimental models of human alcohol use disorder.
Acute or repeated treatment with CGP7930, GS39783, BHF177, rac-BHFF, ADX71441, CMPPE, COR659, ASP8062, KK-92A, and ORM-27669 reduced excessive alcohol drinking, relapse- and binge-like drinking, operant alcohol self-administration, reinstatement of alcohol seeking, and alcohol-induced conditioned place preference in rats and mice.
These effects closely mirrored those of baclofen; notably, they were associated to remarkably lower levels of tolerance and toxicity. The recent transition of ASP8062 to clinical testing will soon prove whether these highly consistent preclinical data translate to AUD patients.
GABAB 受体的正变构调节剂 (PAMs) 构成了 GABAB 受体配体的一个新类别。尽管 GABAB PAMs 显示出更好的安全性特征,但它们复制了正位 GABAB 受体激动剂巴氯芬的几种药理学作用。
本文综述了迄今为止测试的所有 GABAB PAMs 对暴露于经验证的人类酒精使用障碍实验模型的实验室啮齿动物的多种与酒精相关行为的减少或甚至抑制作用。
急性或重复使用 CGP7930、GS39783、BHF177、rac-BHFF、ADX71441、CMPPE、COR659、ASP8062、KK-92A 和 ORM-27669 可减少大鼠和小鼠的过度饮酒、复发样和 binge 样饮酒、操作性酒精自我给药、酒精寻求的复燃以及酒精诱导的条件性位置偏好。
这些作用与巴氯芬非常相似;值得注意的是,它们与明显更低水平的耐受性和毒性相关。最近,ASP8062 已过渡到临床测试,这将很快证明这些高度一致的临床前数据是否适用于 AUD 患者。