Department of Pharmacology and Physiology, Saint Louis University School of Medicine, St. Louis, MO 63104, USA; Henry and Nasrallah Center for Neuroscience, Saint Louis University School of Medicine, St. Louis, MO 63104, USA.
Department of Pharmacology and Physiology, Saint Louis University School of Medicine, St. Louis, MO 63104, USA.
Physiol Behav. 2021 Jun 1;235:113380. doi: 10.1016/j.physbeh.2021.113380. Epub 2021 Mar 8.
The existence of the peptide encoded by the cocaine- and amphetamine-regulated transcript (Cartpt) has been recognized since 1981, but it was not until 1995, that the gene encoding CART peptide (CART) was identified. With the availability of the predicted protein sequence of CART investigators were able to identify sites of peptide localization, which then led to numerous approaches attempting to clarify CART's multiple pharmacologic effects and even provide evidence of potential physiologic relevance. Although not without controversy, a picture emerged of the importance of CART in ingestive behaviors, reward behaviors and even pain sensation. Despite the wealth of data hinting at the significance of CART, in the absence of an identified receptor, the full potential for this peptide or its analogs to be developed into therapeutic agents remained unrealized. There was evidence favoring the action of CART via a G protein-coupled receptor (GPCR), but despite multiple attempts the identity of that receptor eluded investigators until recently. Now with the identification of the previously orphaned GPCR, GPR160, as a receptor for CART, focus on this pluripotent neuropeptide will in all likelihood experience a renaissance and the potential for the development of pharmcotherapies targeting GPR160 seems within reach.
可卡因和安非他命调节转录本(CARTpt)编码的肽的存在自 1981 年以来就已被认识,但直到 1995 年,编码 CART 肽(CART)的基因才被确定。随着 CART 的预测蛋白序列的出现,研究人员能够确定肽的定位部位,这随后导致了许多尝试,试图阐明 CART 的多种药理作用,甚至提供潜在的生理相关性的证据。尽管存在争议,但 CART 在摄食行为、奖励行为甚至疼痛感觉中的重要性已经显现出来。尽管有大量数据表明 CART 的重要性,但由于没有确定的受体,这种肽或其类似物作为治疗剂的全部潜力仍未实现。有证据表明 CART 通过 G 蛋白偶联受体(GPCR)发挥作用,但尽管进行了多次尝试,该受体的身份仍未被研究人员确定,直到最近。现在,先前被认为是孤儿的 GPCR,GPR160,被确定为 CART 的受体,对这种多能神经肽的关注很可能会复兴,针对 GPR160 开发药物治疗的潜力似乎触手可及。