Department of Pharmacology and Physiology and Henry and Amelia Nasrallah Center for Neuroscience Saint Louis University School of Medicine, St Louis, MO 63104, USA.
Endocrinology. 2021 Aug 1;162(8). doi: 10.1210/endocr/bqab108.
Cocaine- and amphetamine-regulated transcript encodes an eponymous peptide, CARTp, which exerts diverse pharmacologic actions in the central and peripheral nervous systems, as well as in several endocrine organs, including pancreas. Here we review those diverse actions, the physiological relevance of which had remained unestablished until recently. With the identification of a CARTp receptor, GPR160, the physiologic importance and therapeutic potential of CARTp or analogs are being revealed. Not only is the CARTp-GPR160 interaction essential for the circadian regulation of appetite and thirst but also for the transmission of nerve injury-induced pain. Molecular approaches now are uncovering additional physiologically relevant actions and the development of acute tissue-specific gene compromise approaches may reveal even more physiologically relevant actions of this pluripotent ligand/receptor pair.
可卡因和苯丙胺调节转录物编码一个同名肽,CARTp,它在中枢和外周神经系统以及包括胰腺在内的几个内分泌器官中发挥多种药理作用。在这里,我们回顾了这些不同的作用,直到最近,这些作用的生理相关性还没有得到确定。随着 CARTp 受体 GPR160 的鉴定,CARTp 或类似物的生理重要性和治疗潜力正在被揭示。不仅 CARTp-GPR160 相互作用对于食欲和口渴的昼夜节律调节至关重要,而且对于神经损伤引起的疼痛的传递也是如此。目前,分子方法正在揭示其他具有生理相关性的作用,急性组织特异性基因缺陷方法的发展可能会揭示这种多能配体/受体对更多具有生理相关性的作用。