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背侧海马中表达的 miR-181a 通过靶向 PRKAA1 调节可卡因 CPP 的复燃。

miR-181a expressed in the dorsal hippocampus regulates the reinstatement of cocaine CPP by targeting PRKAA1.

机构信息

Department of Neurosurgery, Tangdu Hospital, The Fourth Military Medical University, Xi'an, Shaanxi 710038, China; Shaanxi University of Chinese Medicine, Xian Yang, Shaanxi 712046, China.

Xi'an Technological University, Xi'an 710021, China.

出版信息

Behav Brain Res. 2024 Aug 5;471:115097. doi: 10.1016/j.bbr.2024.115097. Epub 2024 Jun 14.

Abstract

Neuroadaptive changes in the hippocampus underlie addictive-like behaviors in humans or animals chronically exposed to cocaine. miR-181a, which is widely expressed in the hippocampus, acts as a regulator for synaptic plasticity, while its role in drug reinstatement is unclear. In this study, we found that miR-181a regulates the reinstatement of cocaine conditioned place preference(CPP), and altered miR-181a expression changes the complexity of hippocampal neurons and the density and morphology of dendritic spines. By using a luciferase gene reporter, we found that miR-181a targets PRKAA1, an upstream molecule in the mTOR pathway. High miR-181a expression reduced the expression of the PRKAA1 mRNA and promoted mTOR activity and the reinstatement of cocaine CPP. These results indicate that miR-181a is involved in neuronal structural plasticity induced by reinstatement of cocaine CPP, possibly through the activation of the mTOR signaling pathway. This study provides new microRNA targets and a theoretical foundation for the prevention of cocaine-induced reinstatement.

摘要

海马体中的神经适应性变化是人类或动物长期接触可卡因后产生类似成瘾行为的基础。miR-181a 在海马体中广泛表达,作为突触可塑性的调节剂,但其在药物复吸中的作用尚不清楚。在这项研究中,我们发现 miR-181a 调节可卡因条件性位置偏好(CPP)的复吸,改变 miR-181a 的表达会改变海马神经元的复杂性以及树突棘的密度和形态。通过使用荧光素酶基因报告,我们发现 miR-181a 靶向 mTOR 通路的上游分子 PRKAA1。高表达的 miR-181a 降低了 PRKAA1 mRNA 的表达,促进了 mTOR 活性和可卡因 CPP 的复吸。这些结果表明,miR-181a 参与了可卡因 CPP 复吸诱导的神经元结构可塑性,可能通过激活 mTOR 信号通路。这项研究为预防可卡因诱导的复吸提供了新的 microRNA 靶点和理论基础。

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