Kumar Jigna Rajesh, Rajkumar Ramamoorthy, Jayakody Tharindunee, Marwari Subhi, Hong Jia Mei, Ma Sherie, Gundlach Andrew L, Lai Mitchell K P, Dawe Gavin S
Department of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
Neurobiology and Ageing Programme, Life Sciences Institute, National University of Singapore, Singapore.
Br J Pharmacol. 2017 May;174(10):1061-1076. doi: 10.1111/bph.13564. Epub 2016 Sep 6.
Relaxin-3 has been proposed to modulate emotional-behavioural functions such as arousal and behavioural activation, appetite regulation, stress responses, anxiety, memory, sleep and circadian rhythm. The nucleus incertus (NI), in the midline tegmentum close to the fourth ventricle, projects widely throughout the brain and is the primary site of relaxin-3 neurons. Over recent years, a number of preclinical studies have explored the function of the NI and relaxin-3 signalling, including reports of mRNA or peptide expression changes in the NI in response to behavioural or pharmacological manipulations, effects of lesions or electrical or pharmacological manipulations of the NI, effects of central microinfusions of relaxin-3 or related agonist or antagonist ligands on physiology and behaviour, and the impact of relaxin-3 gene deletion or knockdown. Although these individual studies reveal facets of the likely functional relevance of the NI and relaxin-3 systems for human physiology and behaviour, the differences observed in responses between species (e.g. rat vs. mouse), the clearly identified heterogeneity of NI neurons and procedural differences between laboratories are some of the factors that have prevented a precise understanding of their function. This review aims to draw attention to the current preclinical evidence available that suggests the relevance of the NI/relaxin-3 system to the pathology and/or symptoms of certain neuropsychiatric disorders and to provide cognizant directions for future research to effectively and efficiently uncover its therapeutic potential.
This article is part of a themed section on Recent Progress in the Understanding of Relaxin Family Peptides and their Receptors. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v174.10/issuetoc.
松弛素-3被认为可调节诸如觉醒和行为激活、食欲调节、应激反应、焦虑、记忆、睡眠和昼夜节律等情绪行为功能。不确定核(NI)位于靠近第四脑室的中线被盖区,广泛投射至全脑,是松弛素-3神经元的主要部位。近年来,多项临床前研究探讨了NI和松弛素-3信号传导的功能,包括关于NI中mRNA或肽表达变化对行为或药理学操作的反应报告、NI损伤或电刺激或药理学操作的影响、向中枢微量注射松弛素-3或相关激动剂或拮抗剂配体对生理和行为的影响,以及松弛素-3基因缺失或敲低的影响。尽管这些单独的研究揭示了NI和松弛素-3系统对人类生理和行为可能具有功能相关性的多个方面,但在不同物种(如大鼠与小鼠)之间观察到的反应差异、NI神经元明确的异质性以及不同实验室之间的操作差异等因素,都阻碍了对其功能的精确理解。本综述旨在引起人们对现有临床前证据的关注,这些证据表明NI/松弛素-3系统与某些神经精神疾病的病理和/或症状相关,并为未来研究提供明确方向,以便有效且高效地发掘其治疗潜力。
本文是关于松弛素家族肽及其受体理解的最新进展主题部分的一部分。要查看本部分的其他文章,请访问http://onlinelibrary.wiley.com/doi/10.1111/bph.v174.10/issuetoc。