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锂作用的机制:新旧发现

The Mechanisms of Lithium Action: The Old and New Findings.

作者信息

Sakrajda Kosma, Rybakowski Janusz K

机构信息

Molecular and Cell Biology Unit, Poznan University of Medical Sciences, 60-572 Poznan, Poland.

Department of Adult Psychiatry, Poznan University of Medical Sciences, 60-572 Poznan, Poland.

出版信息

Pharmaceuticals (Basel). 2025 Mar 26;18(4):467. doi: 10.3390/ph18040467.

Abstract

Despite lithium's presence in modern psychiatry for three-quarters of a century, the mechanisms of its therapeutic action have not been fully elucidated. This article presents the evolution of the views on these mechanisms, and both the old and new findings are discussed. Among the old mechanisms, lithium's effect on the purinergic system; electrolyte metabolism; membrane transport; and second messenger systems, namely, cyclic nucleotide and phosphatidylinositol (PI), glycogen synthase kinase-3beta (GSK-3β), brain-derived neurotrophic factor, and neurotransmitters, are discussed. The new data were obtained from in vitro studies, molecular biology, and genetic research. They showed the effects of lithium on the immune system, biological rhythms, telomere functions, and mitochondria. In this article, each lithium mechanism is considered in the light of its association with the pathogenesis of bipolar disorder or/and as a marker of the lithium response. Although not exhaustive, this review elucidates the multiple potential mechanisms of lithium action. It was also observed that many seemingly "old" mechanisms have experienced a resurgence in research conducted during the 21st century. Additionally, many studies converged on the previously postulated mechanisms of lithium inhibiting GSK-3β and PI.

摘要

尽管锂在现代精神病学领域已存在了四分之三个世纪,但其治疗作用机制尚未完全阐明。本文介绍了对这些机制的观点演变,并对新旧发现进行了讨论。在旧机制中,探讨了锂对嘌呤能系统、电解质代谢、膜转运以及第二信使系统(即环核苷酸和磷脂酰肌醇(PI)、糖原合酶激酶-3β(GSK-3β)、脑源性神经营养因子和神经递质)的影响。新数据来自体外研究、分子生物学和基因研究。这些数据显示了锂对免疫系统、生物节律、端粒功能和线粒体的作用。在本文中,每种锂机制都根据其与双相情感障碍发病机制的关联或/和作为锂反应标志物来进行考量。尽管并不详尽,但本综述阐明了锂作用的多种潜在机制。还观察到,许多看似“旧”的机制在21世纪的研究中重新兴起。此外,许多研究都集中在先前推测的锂抑制GSK-3β和PI的机制上。

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本文引用的文献

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