Rhynchophylline inhibits methamphetamine dependence via modulating the miR-181a-5p/GABRA1 axis

冰毒- 甲基苯丙胺 药理学 离体 有条件地点偏好 体内 拮抗剂 生物碱 化学 小RNA 医学 生物 体外 生物化学 立体化学 生物技术 单体 有机化学 吗啡 丙烯酸酯 基因 聚合物
作者
Mingjin Jiang,Jing Li,Chaohua Luo,Chen Zhu,Zhijie Chen,Wei Bai,Tianyu Hu,Chuan-Hua Feng,Chan Li,Zhixian Mo
出处
期刊:Journal of Ethnopharmacology [Elsevier]
卷期号:314: 116635-116635 被引量:3
标识
DOI:10.1016/j.jep.2023.116635
摘要

Uncaria rhynchophylla (Miq.) Miq. ex Havil. is a plant species that is routinely devoted in traditional Chinese medicine to treat central nervous system disorders. Rhynchophylline (Rhy), a predominant alkaloid isolated from Uncaria rhynchophylla (Miq.) Miq. ex Havil., has been demonstrated to reverse methamphetamine-induced (METH-induced) conditioned place preference (CPP) effects in mice, rats and zebrafish. The precise mechanism is still poorly understood, thus further research is necessary. This study aimed to investigate the role of miRNAs in the inhibitory effect of Rhy on METH dependence. A rat CPP paradigm and a PC12 cell addiction model were established. Microarray assays were used to screen and identify the candidate miRNA. Behavioral assessment, real-time PCR, dual-luciferase reporter assay, western blotting, stereotaxic injection of antagomir/agomir and cell transfection experiments were performed to elucidate the effect of the candidate miRNA and intervention mechanism of Rhy on METH dependence. Rhy successfully reversed METH-induced CPP effect and the upregulated miR-181a-5p expression in METH-dependent rat hippocampus and PC12 cells. Moreover, suppression of miR-181a-5p by antagomir 181a reversed METH-induced CPP effect. Meanwhile, overexpression of miR-181a-5p by agomir 181a in combination with low-dose METH (0.5 mg/kg) elicited a significant CPP effect, which was blocked by Rhy through inhibiting miR-181a-5p. Finally, the result demonstrated that miR-181a-5p exerted its regulatory role by targeting γ-aminobutyric acid A receptor α1 (GABRA1) both in vivo and in vitro. This finding reveals that Rhy inhibits METH dependence via modulating the miR-181a-5p/GABRA1 axis, which may be a promising target for treatment of METH dependence.
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