ACS Chem Neurosci. 2024 Nov 6;15(21):3863-3873. doi: 10.1021/acschemneuro.4c00519. Epub 2024 Oct 9.
Tianeptine () is an unusual antidepressant in that its mechanism of action appears to be independent from any activity at serotonin receptors or monoamine transporters. In fact, tianeptine has been shown to be a moderately potent agonist for the mu opioid receptor (MOR) and to a lesser extent the delta opioid receptor (DOR). Additionally, tianeptine's efficacy may be related to its action on glutamate-mediated pathways of neuroplasticity. Regardless of which neurotransmitter system is primarily responsible for the observed efficacy, the MOR agonist activity is problematic with respect to abuse liability. Increasing numbers of case reports have demonstrated that tianeptine is indeed being used recreationally at doses far beyond what are considered therapeutically relevant or safe, and scheduling reclassifications or outright bans on tianeptine products are ongoing around the world. It is the aim of this review to discuss the medicinal chemistry and pharmacology of tianeptine and to summarize this intriguing discrepancy between tianeptine's historical use as a safe and effective antidepressant and its emerging potential for abuse.
天冬普汀()是一种不同寻常的抗抑郁药,因为其作用机制似乎独立于 5-羟色胺受体或单胺转运体的任何活性。事实上,天冬普汀已被证明是一种中等效力的 μ 阿片受体(MOR)激动剂,对 δ 阿片受体(DOR)的作用较小。此外,天冬普汀的疗效可能与其对谷氨酸介导的神经可塑性途径的作用有关。无论哪种神经递质系统主要负责观察到的疗效,MOR 激动剂活性在滥用倾向方面存在问题。越来越多的病例报告表明,天冬普汀确实在娱乐场所被大量滥用,剂量远远超过治疗相关或安全的剂量,对天冬普汀产品进行重新分类或全面禁止的情况正在全球范围内发生。本文旨在讨论天冬普汀的药物化学和药理学,并总结其作为安全有效的抗抑郁药的历史用途与其潜在滥用之间的这种有趣差异。