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生长激素促分泌素受体对奖赏相关行为的有趣的配体依赖性和非配体依赖性作用

THE INTRIGUING LIGAND-DEPENDENT AND LIGAND-INDEPENDENT ACTIONS OF THE GROWTH HORMONE SECRETAGOGUE RECEPTOR ON REWARD-RELATED BEHAVIORS.

作者信息

Cornejo María P, Mustafá Emilio R, Barrile Franco, Cassano Daniela, De Francesco Pablo N, Raingo Jesica, Perello Mario

机构信息

Laboratory of Neurophysiology of the Multidisciplinary Institute of Cell Biology [IMBICE, Argentine Research Council (CONICET) and Scientific Research Commission, Province of Buenos Aires (CIC-PBA). National University of La Plata], 1900 La Plata, Buenos Aires, Argentina.

Laboratory of Electrophysiology of the IMBICE, 1900 La Plata, Buenos Aires, Argentina.

出版信息

Neurosci Biobehav Rev. 2021 Jan;120:401-416. doi: 10.1016/j.neubiorev.2020.10.017. Epub 2020 Nov 4.

Abstract

The growth hormone secretagogue receptor (GHSR) is a G-protein-coupled receptor (GPCR) highly expressed in the brain, and also in some peripheral tissues. GHSR activity is evoked by the stomach-derived peptide hormone ghrelin and abrogated by the intestine-derived liver-expressed antimicrobial peptide 2 (LEAP2). In vitro, GHSR displays ligand-independent actions, including a high constitutive activity and an allosteric modulation of other GPCRs. Beyond its neuroendocrine and metabolic effects, cumulative evidence shows that GHSR regulates the activity of the mesocorticolimbic pathway and modulates complex reward-related behaviors towards different stimuli. Here, we review current evidence indicating that ligand-dependent and ligand-independent actions of GHSR enhance reward-related behaviors towards appetitive stimuli and drugs of abuse. We discuss putative neuronal networks and molecular mechanisms that GHSR would engage to modulate such reward-related behaviors. Finally, we briefly discuss imaging studies showing that ghrelin would also regulate reward processing in humans. Overall, we conclude that GHSR is a key regulator of the mesocorticolimbic pathway that influences its activity and, consequently, modulates reward-related behaviors via ligand-dependent and ligand-independent actions.

摘要

生长激素促分泌素受体(GHSR)是一种G蛋白偶联受体(GPCR),在大脑以及一些外周组织中高度表达。胃源性肽激素ghrelin可激活GHSR的活性,而肠源性肝脏表达的抗菌肽2(LEAP2)则可使其失活。在体外,GHSR表现出不依赖配体的作用,包括高组成性活性以及对其他GPCR的变构调节。除了其神经内分泌和代谢作用外,越来越多的证据表明,GHSR可调节中脑边缘叶通路的活性,并调节对不同刺激的复杂奖赏相关行为。在此,我们综述当前的证据,表明GHSR的配体依赖性和非配体依赖性作用可增强对食欲性刺激和滥用药物的奖赏相关行为。我们讨论了GHSR可能参与调节此类奖赏相关行为的假定神经网络和分子机制。最后,我们简要讨论了成像研究,这些研究表明ghrelin也可调节人类的奖赏处理。总体而言,我们得出结论,GHSR是中脑边缘叶通路的关键调节因子,它通过配体依赖性和非配体依赖性作用影响该通路的活性,进而调节奖赏相关行为。

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