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锂作为双相情感障碍的神经保护剂:综述

Lithium as a Neuroprotective Agent for Bipolar Disorder: An Overview.

作者信息

Ochoa Enrique L M

机构信息

Department of Psychiatry and Behavioral Sciences, Volunteer Clinical Faculty, University of California at Davis, 2230 Stockton Boulevard, Sacramento, CA, 95817, USA.

出版信息

Cell Mol Neurobiol. 2022 Jan;42(1):85-97. doi: 10.1007/s10571-021-01129-9. Epub 2021 Aug 6.

Abstract

Lithium (Li) is a first option treatment for adult acute episodes of Bipolar Disorder (BD) and for the prophylaxis of new depressed or manic episodes. It is also the preferred choice as maintenance treatment. Numerous studies have shown morphological abnormalities in the brains of BD patients, suggesting that this highly heritable disorder may exhibit progressive and deleterious changes in brain structure. Since treatment with Li ameliorates these abnormalities, it has been postulated that Li is a neuroprotective agent in the same way atypical antipsychotics are neuroprotective in patients diagnosed with schizophrenia spectrum disorders. Li's neuroprotective properties are related to its modulation of nerve growth factors, inflammation, mitochondrial function, oxidative stress, and programmed cell death mechanisms such as autophagy and apoptosis. Notwithstanding, it is not known whether Li-induced neuroprotection is related to the inhibition of its putative molecular targets in a BD episode: the enzymes inositol-monophosphatase, (IMPase), glycogen-synthase-kinase 3β (GSK3), and Protein kinase C (PKC). Furthermore, it is uncertain whether these neuroprotective mechanisms are correlated with Li's clinical efficacy in maintaining mood stability. It is expected that in a nearby future, precision medicine approaches will improve diagnosis and expand treatment options. This will certainly contribute to ameliorating the medical and economic burden created by this devastating mood disorder.

摘要

锂(Li)是双相情感障碍(BD)成人急性发作以及预防新的抑郁或躁狂发作的一线治疗药物。它也是维持治疗的首选。大量研究表明BD患者大脑存在形态学异常,这表明这种高度遗传性疾病可能在脑结构上呈现进行性和有害性变化。由于锂治疗可改善这些异常,因此有人推测锂是一种神经保护剂,就像非典型抗精神病药物对诊断为精神分裂症谱系障碍的患者具有神经保护作用一样。锂的神经保护特性与其对神经生长因子、炎症、线粒体功能、氧化应激以及自噬和凋亡等程序性细胞死亡机制的调节有关。尽管如此,尚不清楚锂诱导的神经保护是否与它在BD发作中对其假定分子靶点(即肌醇单磷酸酶(IMPase)、糖原合酶激酶3β(GSK3)和蛋白激酶C(PKC))的抑制有关。此外,这些神经保护机制是否与锂在维持情绪稳定方面的临床疗效相关也不确定。预计在不久的将来,精准医学方法将改善诊断并扩大治疗选择。这肯定有助于减轻这种毁灭性情绪障碍所造成的医疗和经济负担。

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