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基底外侧杏仁核5-羟色胺2C受体调节慢性甲基苯丙胺给药诱导的情绪障碍相关症状。

Basolateral Amygdala Serotonin 2C Receptor Regulates Emotional Disorder-Related Symptoms Induced by Chronic Methamphetamine Administration.

作者信息

Wang Zhuo, Li Chen, Ding Jiuyang, Li Yanning, Zhou Zhihua, Huang Yanjun, Wang Xiaohan, Fan Haoliang, Huang Jian, He Yitong, Li Jianwei, Chen Jun, Qiu Pingming

机构信息

Department of Infertility and Sexual Medicine, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.

School of Forensic Medicine, Southern Medical University, Guangzhou, China.

出版信息

Front Pharmacol. 2021 Feb 8;12:627307. doi: 10.3389/fphar.2021.627307. eCollection 2021.

Abstract

Globally, methamphetamine (MA) is the second most abused drug, with psychotic symptoms being one of the most common adverse effects. Emotional disorders induced by MA abuse have been widely reported both in human and animal models; however, the mechanisms underlying such disorders have not yet been fully elucidated. In this study, a chronic MA administration mouse model was utilized to elucidate the serotonergic pathway involved in MA-induced emotional disorders. After 4 weeks of MA administration, the animals exhibited significantly increased depressive and anxious symptoms. Molecular and morphological evidence showed that chronic MA administration reduced the expression of the 5-hydroxytryptamine (5-HT) rate-limiting enzyme, tryptophan hydroxylase 2, in the dorsal raphe and the concentrations of 5-HT and its metabolite 5-hydroxyindoleacetic acid in the basolateral amygdala (BLA) nuclei. Alterations in both 5-HT and 5-HT receptor levels occurred simultaneously in BLA; quantitative polymerase chain reaction, western blotting, and fluorescence analysis revealed that the expression of the 5-HT2C receptor (5-HTR) increased. Neuropharmacology and virus-mediated silencing strategies confirmed that targeting 5-HTR reversed the depressive and anxious behaviors induced by chronic MA administration. In the BLA, 5-HTR-positive cells co-localized with GABAergic interneurons. The inactivation of 5-HTR ameliorated impaired GABAergic inhibition and decreased BLA activation. Thus, herein, for the first time, we report that the abnormal regulation of 5-HTR is involved in the manifestation of emotional disorder-like symptoms induced by chronic MA use. Our study suggests that 5-HTR in the BLA is a promising clinical target for the treatment of MA-induced emotional disorders.

摘要

在全球范围内,甲基苯丙胺(MA)是第二大滥用药物,精神病性症状是其最常见的不良反应之一。MA滥用所致的情绪障碍在人类和动物模型中均有广泛报道;然而,此类障碍背后的机制尚未完全阐明。在本研究中,利用慢性给予MA的小鼠模型来阐明参与MA所致情绪障碍的5-羟色胺能通路。给予MA 4周后,动物表现出抑郁和焦虑症状显著增加。分子和形态学证据表明,慢性给予MA可降低中缝背核中5-羟色胺(5-HT)限速酶色氨酸羟化酶2的表达,以及基底外侧杏仁核(BLA)核团中5-HT及其代谢产物5-羟吲哚乙酸的浓度。BLA中5-HT和5-HT受体水平同时发生改变;定量聚合酶链反应、蛋白质免疫印迹和荧光分析显示5-HT2C受体(5-HTR)的表达增加。神经药理学和病毒介导的沉默策略证实,靶向5-HTR可逆转慢性给予MA所致的抑郁和焦虑行为。在BLA中,5-HTR阳性细胞与GABA能中间神经元共定位。5-HTR失活改善了受损的GABA能抑制并降低了BLA的激活。因此,我们首次在此报告,5-HTR的异常调节参与了慢性使用MA所致的情绪障碍样症状的表现。我们的研究表明,BLA中的5-HTR是治疗MA所致情绪障碍的一个有前景的临床靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/def2/7897655/61f45899ccc8/fphar-12-627307-g001.jpg

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