Chronic Stress-Induced Elevation of Melanin-Concentrating Hormone in the Locus Coeruleus Inhibits Norepinephrine Production and Associated With Depression-Like Behaviors in Rats.

IF 4.5 2区 医学 Q1 CLINICAL NEUROLOGY
Nurhumar Kurban, Yu Qin, Hui-Ling Zhao, Xiao Hu, Xi Chen, Yi-Yi Zhao, Yu-Shuo Peng, Hong-Bo Wang, Su-Ying Cui, Yong-He Zhang
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Abstract

Background: Melanin-concentrating hormone (MCH) is a hypothalamic neuropeptide that projects throughout the central nervous system, including the noradrenergic locus coeruleus (LC). Our previous study suggested that MCH/MCH receptor 1 (MCHR1) in the LC may be involved in the regulation of depression. The present study investigated whether the role of MCH/MCHR1 in the LC in depression-like behaviors is associated with the regulation of norepinephrine.

Method: Chronic unpredictable stress (CUS) and an acute intra-LC microinjection of MCH induced depression-like behaviors in rats. The MCHR1 antagonist SNAP-94847 was also microinjected in the LC in rats that were suffering CUS or treated with MCH. The sucrose preference, forced swim, and locomotor tests were used for behavioral evaluation. Immunofluorescence staining, enzyme-linked immunosorbent assay, western blot, and high-performance liquid chromatography with electrochemical detection were used to explore the mechanism of MCH/MCHR1 in the regulation of depression-like behaviors.

Results: CUS induced an abnormal elevation of MCH levels and downregulated MCHR1 in the LC, which was highly correlated with the formation of depression-like behaviors. SNAP-94847 exerted antidepressant effects in CUS-exposed rats by normalizing tyrosine hydroxylase, dopamine β hydroxylase, and norepinephrine in the LC. An acute microinjection of MCH induced depression-like behaviors through its action on MCHR1. MCHR1 antagonism in the LC significantly reversed the MCH-induced downregulation of norepinephrine production by normalizing MCHR1-medicated cAMP-PKA signaling.

Conclusions: Our study confirmed that the MCH/MCHR1 system in the LC may be involved in depression-like behaviors by downregulating norepinephrine production. These results improve our understanding of the pathogenesis of depression that is related to the MCH/MCHR1 system in the LC.

慢性应激诱导的黑色素浓缩荷尔蒙在大鼠神经节位置的升高会抑制去甲肾上腺素的分泌,并与抑郁样行为相关。
背景:黑色素浓缩激素(MCH)是一种下丘脑神经肽,可投射到整个中枢神经系统,包括去甲肾上腺素能区(LC)。我们之前的研究表明,LC 中的 MCH/MCH 受体 1(MCHR1)可能参与了抑郁症的调控。本研究探讨了MCH/MCHR1在抑郁样行为中的作用是否与去甲肾上腺素的调节有关:方法:慢性不可预测应激(CUS)和急性LC内显微注射MCH诱导大鼠抑郁样行为。此外,还在大鼠LC内注射了MCHR1拮抗剂SNAP-94847。行为评估采用了蔗糖偏好、强迫游泳和运动试验。采用免疫荧光染色、ELISA、Western blot和HPLC-ECD等方法探讨MCH/MCHR1在抑郁样行为中的调控机制:结果:CUS诱导LC中MCH水平异常升高并下调MCHR1,这与抑郁样行为的形成高度相关。SNAP-94847通过使LC中的酪氨酸羟化酶、多巴胺β羟化酶和去甲肾上腺素正常化,对暴露于CUS的大鼠产生抗抑郁作用。通过对 MCHR1 的作用,MCH 的急性显微注射可诱导抑郁样行为。在LC中拮抗MCHR1可使MCHR1介导的cAMP-PKA信号转导正常化,从而显著逆转MCH诱导的去甲肾上腺素分泌下调:我们的研究证实,LC 中的 MCH/MCHR1 系统可能通过下调去甲肾上腺素的分泌参与了抑郁样行为。这些结果加深了我们对与 LC 中 MCH/MCHR1 系统有关的抑郁症发病机制的理解。
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来源期刊
CiteScore
8.40
自引率
2.10%
发文量
230
审稿时长
4-8 weeks
期刊介绍: The central focus of the journal is on research that advances understanding of existing and new neuropsychopharmacological agents including their mode of action and clinical application or provides insights into the biological basis of psychiatric disorders and thereby advances their pharmacological treatment. Such research may derive from the full spectrum of biological and psychological fields of inquiry encompassing classical and novel techniques in neuropsychopharmacology as well as strategies such as neuroimaging, genetics, psychoneuroendocrinology and neuropsychology.
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