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代谢型谷氨酸受体在神经内分泌功能调控中的作用。

Role of metabotropic glutamate receptors in the control of neuroendocrine function.

作者信息

Durand Daniela, Pampillo Macarena, Caruso Carla, Lasaga Mercedes

机构信息

Research Center in Reproduction, School of Medicine, University of Buenos Aires, Paraguay 2155, Piso 10, 1121 Buenos Aires, Argentina.

出版信息

Neuropharmacology. 2008 Sep;55(4):577-83. doi: 10.1016/j.neuropharm.2008.06.022. Epub 2008 Jun 20.

Abstract

Glutamate exerts its effects through binding and activation of two classes of specific receptors: ionotropic (iGluRs) and metabotropic (mGluRs). Group I mGluR includes mGluR1 and mGluR5 subtypes, group II includes mGluR2 and mGluR3 subtypes and group III includes the subtypes mGluR 4, 6, 7 and 8. Glutamate and its receptors are found in all key hypothalamic areas critically involved in reproduction and neuroendocrine function. To date, considerable data support an important role for iGluRs in the control of neuroendocrine function; however, the role of mGluRs as regulators of hypothalamic-pituitary function has not been clearly elucidated. mGluRs could be exerting a fine tune on the release of hypothalamic factors that regulate hormone release such as Substance P, GABA, alpha-MSH and CRH. Group II mGluR exert a direct inhibitory effect on anterior pituitary prolactin and GH secretion. Moreover, some group II mGluR agonists, like LY 354,740 and LY 379,268, can modulate PRL secretion from the anterior pituitary through their actions as dopamine receptor agonists. Evidence suggests a role for group III mGluR subtypes in stress-related behavioral disorders. Several reports indicate that selective ligands for mGluR subtypes have potential for the treatment of a wide variety of neurological and psychiatric disorders, including depression, anxiety disorders, schizophrenia, epilepsy and Alzheimer's disease among others. Since converging lines of evidence suggest a role for mGluRs subtypes in neuroendocrine regulation of hormone secretion, mGluRs neuroendocrine actions must be taken in consideration to insure proper treatment of these diseases. Moreover, discovery of selective agonists provides an opportunity to investigate the physiological role of mGluR subtypes and to directly test the neuroendocrine actions of mGluRs. Finally, mGluRs selective agonists may have an impact in the treatment of conditions involving chronic stress, such as depression and anxiety disorders, since they regulate neuroendocrine stress circuits involving the HPA axis and stress-sensitive hormones such as oxytocin and prolactin. This review aims to provide a survey of our current understanding of the effects of mGluR activation on neuroendocrine function.

摘要

谷氨酸通过与两类特定受体结合并激活来发挥其作用

离子型(离子型谷氨酸受体,iGluRs)和代谢型(代谢型谷氨酸受体,mGluRs)。I组代谢型谷氨酸受体包括mGluR1和mGluR5亚型,II组包括mGluR2和mGluR3亚型,III组包括mGluR4、6、7和8亚型。谷氨酸及其受体存在于下丘脑所有关键区域,这些区域在生殖和神经内分泌功能中起关键作用。迄今为止,大量数据支持离子型谷氨酸受体在神经内分泌功能控制中起重要作用;然而,代谢型谷氨酸受体作为下丘脑 - 垂体功能调节因子的作用尚未得到明确阐明。代谢型谷氨酸受体可能对调节激素释放的下丘脑因子如P物质、γ-氨基丁酸、α-促黑素和促肾上腺皮质激素释放激素的释放起到微调作用。II组代谢型谷氨酸受体对垂体前叶催乳素和生长激素分泌具有直接抑制作用。此外,一些II组代谢型谷氨酸受体激动剂,如LY 354,740和LY 379,268,可通过作为多巴胺受体激动剂的作用来调节垂体前叶催乳素的分泌。有证据表明III组代谢型谷氨酸受体亚型在与应激相关的行为障碍中起作用。几份报告表明,代谢型谷氨酸受体亚型的选择性配体具有治疗多种神经和精神疾病的潜力,包括抑郁症、焦虑症、精神分裂症、癫痫和阿尔茨海默病等。由于越来越多的证据表明代谢型谷氨酸受体亚型在激素分泌的神经内分泌调节中起作用,因此在确保对这些疾病进行适当治疗时必须考虑代谢型谷氨酸受体的神经内分泌作用。此外,选择性激动剂的发现为研究代谢型谷氨酸受体亚型的生理作用以及直接测试代谢型谷氨酸受体的神经内分泌作用提供了机会。最后,代谢型谷氨酸受体选择性激动剂可能对涉及慢性应激的疾病如抑郁症和焦虑症的治疗产生影响,因为它们调节涉及下丘脑 - 垂体 - 肾上腺轴和应激敏感激素如催产素和催乳素的神经内分泌应激回路。本综述旨在概述我们目前对代谢型谷氨酸受体激活对神经内分泌功能影响的理解。

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