The orphan G protein-coupled receptor, GPR139, is expressed in the hypothalamus and is involved in the regulation of body mass, blood glucose, and insulin

被引:5
作者
Nogueira, Pedro A. S. [1 ]
Moura-Assis, Alexandre [1 ]
Zanesco, Ariane M. [1 ]
Bombassaro, Bruna [1 ]
Gallo-Ferraz, Ana L. [1 ]
Simoes, Marcela R. [1 ]
Engel, Daiane F. [1 ,2 ]
Razolli, Daniela S. [1 ]
Gaspar, Joana M. [1 ,3 ]
Donato Junior, Jose [4 ]
Velloso, Licio A. [1 ,5 ]
机构
[1] Univ Estadual Campinas, Obes & Comorbid Res Ctr, Lab Cell Signaling, Campinas, Brazil
[2] Univ Fed Ouro Preto, Sch Pharm, Ouro Preto, MG, Brazil
[3] Univ Fed Santa Catarina, Sch Biol Sci, Dept Biochem, Florianopolis, SC, Brazil
[4] Univ Sao Paulo, Inst Biomed Sci, Dept Physiol & Biophys, Sao Paulo, Brazil
[5] Natl Inst Sci & Technol Neuroimmunomodulat, Rio De Janeiro, Brazil
基金
巴西圣保罗研究基金会;
关键词
Obesity; Caloric intake; Energy expenditure; Proopiomelanocortin; G-protein-coupled receptor; ENERGY-BALANCE; AMINO-ACIDS; FOOD-INTAKE; NARCOLEPSY; DISCOVERY; SLEEP; INHIBITION; SUVOREXANT; GENETICS; INSOMNIA;
D O I
10.1016/j.neulet.2022.136955
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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.
引用
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页数:8
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共 40 条
[1]   Toward a Wiring Diagram Understanding of Appetite Control [J].
Andermann, Mark L. ;
Lowell, Bradford B. .
NEURON, 2017, 95 (04) :757-778
[2]   Narcolepsy in orexin knockout mice:: Molecular genetics of sleep regulation [J].
Chemelli, RM ;
Willie, JT ;
Sinton, CM ;
Elmquist, JK ;
Scammell, T ;
Lee, C ;
Richardson, JA ;
Williams, SC ;
Xiong, YM ;
Kisanuki, Y ;
Fitch, TE ;
Nakazato, M ;
Hammer, RE ;
Saper, CB ;
Yanagisawa, M .
CELL, 1999, 98 (04) :437-451
[3]   Hindbrain circuits in the control of eating behaviour and energy balance [J].
Cheng, Wenwen ;
Gordian, Desiree ;
Ludwig, Mette Q. ;
Pers, Tune H. ;
Seeley, Randy J. ;
Myers, Martin G., Jr. .
NATURE METABOLISM, 2022, 4 (07) :826-835
[4]   AMPK is essential for energy homeostasis regulation and glucose sensing by POMC and AgRP neurons [J].
Claret, Marc ;
Smith, Mark A. ;
Batterham, Rachel L. ;
Selman, Colin ;
Choudhury, Agharul I. ;
Fryer, Lee G. D. ;
Clements, Melanie ;
Al-Qassab, Hind ;
Heffron, Helen ;
Xu, Allison W. ;
Speakman, John R. ;
Barsh, Gregory S. ;
Viollet, Benoit ;
Vaulont, Sophie ;
Ashford, Michael L. J. ;
Carling, David ;
Withers, Dominic J. .
JOURNAL OF CLINICAL INVESTIGATION, 2007, 117 (08) :2325-2336
[5]   A central thermogenic-like mechanism in feeding regulation: An interplay between arcuate nucleus T3 and UCP2 [J].
Coppola, Anna ;
Liu, Zhong-Wu ;
Andrews, Zane B. ;
Paradis, Eric ;
Roy, Marie-Claude ;
Friedman, Jeffrey M. ;
Ricquier, Daniel ;
Richard, Denis ;
Horvath, Tamas L. ;
Gao, Xiao-Bing ;
Diano, Sabrina .
CELL METABOLISM, 2007, 5 (01) :21-33
[6]   Integration of NPY, AGRP, and melanocortin signals in the hypothalamic paraventricular nucleus: Evidence of a cellular basis for the adipostat [J].
Cowley, MA ;
Pronchuk, N ;
Fan, W ;
Dinulescu, DM ;
Colmers, WF ;
Cone, RD .
NEURON, 1999, 24 (01) :155-163
[7]   The partial inhibition of hypothalamic IRX3 exacerbates obesity [J].
de Araujo, Thiago Matos ;
Razolli, Daniela S. ;
Correa-da-Silva, Felipe ;
de Lima-Junior, Jose C. ;
Gaspar, Rodrigo S. ;
Sidarta-Oliveira, Davi ;
Victorio, Sheila C. ;
Donato, Jose, Jr. ;
Kim, Young-Bum ;
Velloso, Licio A. .
EBIOMEDICINE, 2019, 39 :448-460
[8]   UCP2 protects hypothalamic cells from TNF-α-induced damage [J].
Degasperi, Giovanna R. ;
Romanatto, Talita ;
Denis, Raphael G. P. ;
Araujo, Eliana P. ;
Moraes, Juliana C. ;
Inada, Natalia M. ;
Vercesi, Anibal E. ;
Velloso, Licio A. .
FEBS LETTERS, 2008, 582 (20) :3103-3110
[9]   Feeding signals and brain circuitry [J].
Dietrich, Marcelo O. ;
Horvath, Tamas L. .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2009, 30 (09) :1688-1696
[10]   Central Regulation of Metabolism by Growth Hormone [J].
Donato, Jose, Jr. ;
Wasinski, Frederick ;
Furigo, Isadora C. ;
Metzger, Martin ;
Frazao, Renata .
CELLS, 2021, 10 (01) :1-14