School of Pharmaceutical Sciences of Ribeirao Preto (FCFRP), University of Sao Paulo (USP), Ribeirao Preto, Brazil.
Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.
Basic Clin Pharmacol Toxicol. 2021 Jul;129(1):3-14. doi: 10.1111/bcpt.13595. Epub 2021 May 17.
The endocannabinoid 2-arachidonoylglycerol (2-AG) is an atypical neurotransmitter synthesized on demand in response to a wide range of stimuli, including exposure to stress. Through the activation of cannabinoid receptors, 2-AG can interfere with excitatory and inhibitory neurotransmission in different brain regions and modulate behavioural, endocrine and emotional components of the stress response. Exposure to chronic or intense unpredictable stress predisposes to maladaptive behaviour and is one of the main risk factors involved in developing mood disorders, such as major depressive disorder (MDD). In this review, we describe the molecular mechanisms involved in 2-AG signalling in the brain of healthy and stressed animals and discuss how such mechanisms could modulate stress adaptation and susceptibility to depression. Furthermore, we review preclinical evidence indicating that the pharmacological modulation of 2-AG signalling stands as a potential new therapeutic target in treating MDD. Particular emphasis is given to the pharmacological augmentation of 2-AG levels by monoacylglycerol lipase (MAGL) inhibitors and the modulation of CB2 receptors.
内源性大麻素 2-花生四烯酸甘油酯 (2-AG) 是一种非典型神经递质,可根据需要合成以响应各种刺激,包括暴露于压力之下。通过激活大麻素受体,2-AG 可以干扰不同脑区的兴奋性和抑制性神经传递,并调节应激反应的行为、内分泌和情绪成分。暴露于慢性或强烈的不可预测的压力会导致适应不良的行为,这是导致情绪障碍(如重度抑郁症 (MDD) 的主要风险因素之一。在这篇综述中,我们描述了 2-AG 信号在健康和应激动物大脑中的分子机制,并讨论了这些机制如何调节应激适应和对抑郁的易感性。此外,我们还回顾了临床前证据,表明 2-AG 信号的药理学调节是治疗 MDD 的潜在新治疗靶点。特别强调了通过单酰基甘油脂肪酶 (MAGL) 抑制剂增加 2-AG 水平和调节 CB2 受体的药理学方法。