Laboratory of Cell Signaling-Obesity and Comorbidities Research Center, University of Campinas, Campinas, Brazil.
Department of Physiology and Biophysics, Institute of Biomedical Sciences, University of Sao Paulo, Sao Paulo, Brazil.
Neurosci Lett. 2022 Jun 11;781:136660. doi: 10.1016/j.neulet.2022.136660. Epub 2022 Apr 27.
Currently, up to 35% off all drugs approved for the treatment of human diseases belong to the G-protein-coupled receptor (GPCR) family. Out of the almost 800 existing GPCRs, 25% have no known endogenous ligands and are regarded as orphan receptors; many of these are currently under investigation as potential pharmacological targets. Here, we hypothesised that orphan GPCRs expressed in the hypothalamus could be targets for the treatment of obesity and other metabolic diseases. Using bioinformatic tools, we identified 78 class A orphan GPCRs that are expressed in the hypothalamus of mice. Initially, we selected two candidates and determined their responsivities to nutritional interventions: GPR162, the GPCR with highest expression in the hypothalamus, and GPR68, a GPCR with intermediate expression in the hypothalamus and that has never been explored for its potential involvement in metabolic regulation. GPR162 expression was not modified by fasting/feeding or by the consumption of a high-fat diet, and was therefore not subsequently evaluated. Conversely, GPR68 expression increased in response to the consumption of a high-fat diet and reduced under fasting conditions. Using immunofluorescence, GPR68 was identified in both proopiomelanocortin-expressing and agouti-related peptide-expressing neurons in the hypothalamic arcuate nucleus. Acute inhibition of GPR68 with an allosteric modulator promoted an increase in the expression of the orexigenic agouti-related peptide and neuropeptide Y, whereas 4- and 12-h inhibition of GPR68 resulted in increased caloric intake. Thus, GPR68 has emerged as an orphan GPCR that is expressed in the hypothalamus and is involved in the regulation of feeding.
目前,用于治疗人类疾病的所有获批药物中,有多达 35%属于 G 蛋白偶联受体(GPCR)家族。在现有的近 800 种 GPCR 中,有 25%没有已知的内源性配体,被认为是孤儿受体;其中许多目前正在被研究作为潜在的药理学靶点。在这里,我们假设在下丘脑中表达的孤儿 GPCR 可能是治疗肥胖症和其他代谢疾病的靶点。使用生物信息学工具,我们鉴定出 78 种在小鼠下丘脑表达的 A 类孤儿 GPCR。最初,我们选择了两个候选者,并确定了它们对营养干预的反应性:GPR162,在下丘脑中表达最高的 GPCR,和 GPR68,在下丘脑中表达中等的 GPCR,并且从未探索过其在代谢调节中的潜在作用。GPR162 的表达不受禁食/进食或高脂肪饮食的影响,因此未进行后续评估。相反,GPR68 的表达在高脂肪饮食的消耗下增加,在禁食条件下减少。通过免疫荧光,在下丘脑弓状核中发现 GPR68 存在于表达前阿黑皮素原的神经元和表达刺鼠相关肽的神经元中。用别构调节剂急性抑制 GPR68 可促进食欲性刺鼠相关肽和神经肽 Y 的表达增加,而 GPR68 的 4 小时和 12 小时抑制导致热量摄入增加。因此,GPR68 作为一种在下丘脑中表达并参与进食调节的孤儿 GPCR 而出现。