Nogueira Pedro A S, Moura-Assis Alexandre, Zanesco Ariane M, Bombassaro Bruna, Gallo-Ferraz Ana L, Simões Marcela R, Engel Daiane F, Razolli Daniela S, Gaspar Joana M, Junior Jose Donato, Velloso Licio A
Laboratory of Cell Signaling-Obesity and Comorbidities Research Center, University of Campinas, Campinas, Brazil.
Laboratory of Cell Signaling-Obesity and Comorbidities Research Center, University of Campinas, Campinas, Brazil; School of Pharmacy, Federal University of Ouro Preto, Minas Gerais, Brazil.
Neurosci Lett. 2023 Jan 1;792:136955. doi: 10.1016/j.neulet.2022.136955. Epub 2022 Nov 5.
GPR139 is an orphan G-protein-coupled receptor that is expressed in restricted areas of the nervous system, including the hypothalamus. In this study, we hypothesized that GPR139 could be involved in the regulation of energy balance and metabolism. In the first part of the study, we confirmed that GPR139 is expressed in the hypothalamus and particularly in proopiomelanocortin and agouti-related peptide neurons of the mediobasal hypothalamus. Using a lentivirus with a short-hairpin RNA, we inhibited the expression of GPR139 bilaterally in the mediobasal hypothalamus of mice. The intervention promoted a 40% reduction in the hypothalamic expression of GPR139, which was accompanied by an increase in body mass, a reduction in fasting blood glucose levels, and an increase in insulin levels. In the hypothalamus, inhibition of GPR139 was accompanied by a reduction in the expression of orexin. As previous studies using a pharmacological antagonist of orexin showed a beneficial impact on type 2 diabetes and glucose metabolism, we propose that the inhibition of hypothalamic GPR139 could be acting indirectly through the orexin system to control systemic glucose and insulin. In conclusion, this study advances the characterization of GPR139 in the hypothalamus, demonstrating its involvement in the regulation of body mass, blood insulin, and glycemia.
GPR139是一种孤儿G蛋白偶联受体,在包括下丘脑在内的神经系统特定区域表达。在本研究中,我们假设GPR139可能参与能量平衡和代谢的调节。在研究的第一部分,我们证实GPR139在下丘脑中表达,特别是在中基底下丘脑的阿片-促黑素细胞皮质素原和刺鼠相关肽神经元中表达。我们使用携带短发夹RNA的慢病毒,双侧抑制小鼠中基底下丘脑中GPR139的表达。该干预使下丘脑GPR139的表达降低了40%,同时伴有体重增加、空腹血糖水平降低和胰岛素水平升高。在下丘脑中,GPR139的抑制伴随着食欲素表达的降低。由于先前使用食欲素药理学拮抗剂的研究显示对2型糖尿病和葡萄糖代谢有有益影响,我们提出抑制下丘脑GPR139可能通过食欲素系统间接作用来控制全身葡萄糖和胰岛素。总之,本研究推进了对下丘脑中GPR139的表征,证明其参与体重、血液胰岛素和血糖的调节。