Wang Zhuo, Zheng Rui, Wang Xiaohan, Huang Xuekun, Huang Jian, Gu Cihang, He Yitong, Wu Shuo, Chen Jingyuan, Yang Qintai, Qiu Pingming
Department of Infertility and Sexual Medicine, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Guangzhou Key Laboratory of Forensic Multi-Omics for Precision Identification, School of Forensic Medicine, Southern Medical University, Guangzhou, China.
Front Mol Neurosci. 2022 May 2;15:884790. doi: 10.3389/fnmol.2022.884790. eCollection 2022.
Methamphetamine (Meth) is a predominantly abused neurostimulant, and its abuse is often associated with multiple neurological symptoms. Olfaction, the sense of smell, is a highly neurotransmission-dependent physiological process; however, the effect of Meth on olfactory function and its underlying mechanisms remain largely unknown. This study aimed to explore the impact of Meth abuse on the olfactory system and the potential mechanisms. Chronic Meth abuse was induced by daily administration of Meth in male mice for 4 weeks, and we then systematically examined olfactory performance. Behavioral tests found that Meth-treated animals showed increased olfactory threshold, decreased olfactory sensitivity, reduced olfactory-dependent discrimination, and difficulty in seeking buried food. Notably, the increased deposition of α-synuclein (α-syn) in the olfactory bulb was detected. Adeno-associated virus (AAV)-mediated α-syn intervention therapy in the olfactory bulb significantly alleviated Meth-induced olfactory function impairment, and 8 weeks of aerobic exercise showed similar effects through the same principle of α-syn intervention. Notably, exercise-mediated reduction of α-syn inhibited abnormal firing activity and restored the inhibitory synaptic regulation of mitral cells in the olfactory bulb. These findings suggest the involvement of α-syn in the pathogenic mechanisms of Meth-induced olfactory dysfunction and shed light on the possible therapeutic applications of aerobic exercise in Meth-induced olfactory dysfunction.
甲基苯丙胺(冰毒)是一种主要被滥用的神经兴奋剂,其滥用往往与多种神经症状相关。嗅觉,即嗅觉功能,是一个高度依赖神经传递的生理过程;然而,冰毒对嗅觉功能的影响及其潜在机制在很大程度上仍不清楚。本研究旨在探讨冰毒滥用对嗅觉系统的影响及其潜在机制。通过每天给雄性小鼠注射冰毒4周诱导慢性冰毒滥用,然后我们系统地检测嗅觉表现。行为测试发现,接受冰毒治疗的动物嗅觉阈值升高、嗅觉敏感性降低、嗅觉依赖性辨别能力下降以及寻找埋藏食物困难。值得注意的是,检测到嗅球中α-突触核蛋白(α-syn)的沉积增加。腺相关病毒(AAV)介导的嗅球α-syn干预治疗显著减轻了冰毒诱导的嗅觉功能损害,并且8周的有氧运动通过相同的α-syn干预原理显示出类似的效果。值得注意的是,运动介导的α-syn减少抑制了异常放电活动,并恢复了嗅球中二尖瓣细胞的抑制性突触调节。这些发现表明α-syn参与了冰毒诱导的嗅觉功能障碍的致病机制,并为有氧运动在冰毒诱导的嗅觉功能障碍中的可能治疗应用提供了线索。