Positive allosteric modulators of the GABAB receptor: a new class of ligands with therapeutic potential for alcohol use disorder

被引:1
|
作者
Colombo, Giancarlo [1 ,2 ]
机构
[1] Natl Res Council Italy, Neurosci Inst, Sect Cagliari, I-09042 Monserrato, CA, Italy
[2] Natl Res Council Italy, Neurosci Inst, Sect Cagliari, SS 55,km 4,500, I-09042 Monserrato, CA, Italy
来源
ALCOHOL AND ALCOHOLISM | 2024年 / 59卷 / 03期
关键词
GABAB receptor; positive allosteric modulators; baclofen; alcohol-related behaviours; animal models of alcohol use disorder; ANIMAL-MODELS; B RECEPTOR; MOTIVATIONAL PROPERTIES; RAC-BHFF; SP RATS; BACLOFEN; GS39783; ETHANOL; REDUCTION; SEEKING;
D O I
10.1093/alcalc/agae018
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
Background: 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. Aims: 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. Results: 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. Conclusions: 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.
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页数:9
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