Wang Jing, Hao Yulei, Ma Di, Feng Liangshu, Yang Feng, An Pingxu, Su Xingqi, Feng Jiachun
Department of Neurology and Neuroscience Center, The First Hospital of Jilin University, Changchun, Jilin, China.
Department of Neurology, Jining First People's Hospital, Jining, Shandong, China.
Front Pharmacol. 2025 Feb 17;16:1526270. doi: 10.3389/fphar.2025.1526270. eCollection 2025.
The recreational abuse of addictive drugs poses considerable challenges to public health, leading to widespread neurotoxicity and neurological dysfunction. This review comprehensively examines the neurotoxic mechanisms, clinical manifestations, and treatment strategies associated with six commonly abused substances: methamphetamine, cocaine, synthetic cathinones, ketamine, nitrous oxide and heroin. Despite their diverse pharmacological properties, these drugs converge on shared neurotoxic pathways, including oxidative stress, mitochondrial dysfunction, excitotoxicity, and neuroinflammation. Psychostimulants, such as methamphetamine, cocaine and synthetic cathinones, disrupt monoaminergic neurotransmission, causing cognitive impairment, psychiatric disturbances, and neurovascular damage. Dissociative anesthetics, including ketamine and nitrous oxide, impair glutamatergic transmission and mitochondrial function, thereby exacerbating excitotoxicity and neuronal apoptosis. Opioids, such as heroin, primarily target the brain's reward system and induce oxidative stress, neuroinflammation, and cerebrovascular complications. Treatment strategies remain limited, focusing on symptomatic management, neuroprotective interventions, and behavioral therapies. Emerging approaches, such as antioxidants, NMDA receptor modulators, and cognitive rehabilitation, show promise but require further validation. By highlighting the underlying mechanisms and therapeutic challenges, this review provides a foundation for developing targeted interventions and advancing research on drug-induced neurotoxicity.
成瘾性药物的娱乐性滥用对公共卫生构成了巨大挑战,导致广泛的神经毒性和神经功能障碍。本综述全面研究了与六种常见滥用物质相关的神经毒性机制、临床表现和治疗策略,这六种物质分别是甲基苯丙胺、可卡因、合成卡西酮、氯胺酮、一氧化二氮和海洛因。尽管这些药物具有不同的药理特性,但它们都汇聚于共同的神经毒性途径,包括氧化应激、线粒体功能障碍、兴奋性毒性和神经炎症。精神兴奋剂,如甲基苯丙胺、可卡因和合成卡西酮,会破坏单胺能神经传递,导致认知障碍、精神障碍和神经血管损伤。分离性麻醉剂,包括氯胺酮和一氧化二氮,会损害谷氨酸能传递和线粒体功能,从而加剧兴奋性毒性和神经元凋亡。阿片类药物,如海洛因,主要作用于大脑的奖赏系统,并引发氧化应激、神经炎症和脑血管并发症。治疗策略仍然有限,主要集中在对症治疗、神经保护干预和行为疗法。新兴方法,如抗氧化剂、NMDA受体调节剂和认知康复,显示出前景,但需要进一步验证。通过强调潜在机制和治疗挑战,本综述为制定有针对性的干预措施和推进药物诱导神经毒性的研究提供了基础。