Section on Medicinal Chemistry, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, 5625 Fishers Lane, Rockville, MD 20852, USA.
Laboratory of Biophotonics and Quantum Biology, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, 5625 Fishers Lane, Rockville, MD 20852, USA.
Int J Mol Sci. 2024 May 3;25(9):5012. doi: 10.3390/ijms25095012.
Cannabinoid receptors CBR and CBR are G-protein coupled receptors acted upon by endocannabinoids (eCBs), namely 2-arachidonoylglycerol (2-AG) and -arachidonoyl ethanolamine (AEA), with unique pharmacology and modulate disparate physiological processes. A genetically encoded GPCR activation-based sensor that was developed recently-GRAB-has been shown to be capable of monitoring real-time changes in eCB levels in cultured cells and preclinical models. However, its responsiveness to exogenous synthetic cannabinoid agents, particularly antagonists and allosteric modulators, has not been extensively characterized. This current study expands upon the pharmacological characteristics of GRAB to enhance the understanding of fluorescent signal alterations in response to various functionally indiscriminate cannabinoid ligands. The results from this study could enhance the utility of the GRAB sensor for in vitro as well as in vivo studies of cannabinoid action and may aid in the development of novel ligands.
大麻素受体 CBR 和 CBR 是 G 蛋白偶联受体,受内源性大麻素(eCBs)的作用,即 2-花生四烯酸甘油(2-AG)和 -花生四烯酸乙醇胺(AEA),具有独特的药理学特性,并调节不同的生理过程。最近开发的一种基于基因编码的 GPCR 激活的传感器-GRAB-已被证明能够在培养细胞和临床前模型中监测 eCB 水平的实时变化。然而,它对外源合成大麻素药物,特别是拮抗剂和变构调节剂的反应性尚未得到广泛表征。本研究扩展了 GRAB 的药理学特征,以增强对各种功能上无差别的大麻素配体响应荧光信号变化的理解。本研究的结果可以提高 GRAB 传感器在大麻素作用的体外和体内研究中的实用性,并可能有助于新型配体的开发。