阿那达胺
导水管周围灰质
内大麻素系统
心理学
抗焦虑药
大麻素
大麻素受体
厌恶性刺激
单酰甘油脂肪酶
神经科学
化学
药理学
焦虑
医学
敌手
受体
中枢神经系统
精神科
生物化学
中脑
作者
Rayssa C. Briânis,Rita Lima,Fabrício A. Moreira,Daniele C. Aguiar
标识
DOI:10.1097/fbp.0000000000000639
摘要
The endocannabinoid system modulates the stress coping strategies in the dorsolateral periaqueductal grey (dlPAG). The most relevant endocannabinoids, anandamide and 2-arachidonoylglycerol (2-AG) exert inhibitory control over defensive reactions mediated by the dlPAG. However, the protective role of anandamide is limited by its lack of effect in higher concentrations. Thus, the 2-AG emerges as a complementary target for developing new anxiolytic compounds. Nevertheless, the role of 2-AG on stress responsivity may vary according to the nature of the stimulus. In this study, we verified whether the dlPAG injection of 2-AG or inhibitors of its hydrolysis induce anxiolytic-like effects in male Wistar rats exposed to behavioral models in which physical stress (mild electric shock) is a critical component, namely the contextual fear conditioning test (CFC) and the Vogel conflict test (VCT). We also investigated the contribution of cannabinoid receptor type 1 (CB 1 ) and type 2 (CB 2 ) in such effects. The facilitation of 2-AG signaling in the dlPAG reduced contextual fear expression and exhibited an anxiolytic-like effect in the VCT in a mechanism dependent on activation of CB 1 and CB 2 . However, the VCT required a higher dose than CFC. Further, the monoacylglycerol inhibitors, which inhibit the hydrolysis of 2-AG, were effective only in the CFC. In conclusion, we confirmed the anti-aversive properties of 2-AG in the dlPAG through CB 1 and CB 2 mechanisms. However, these effects could vary according to the type of stressor and the anxiety model employed.
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