Forlenza O V, De-Paula V J R, Diniz B S O
†Laboratory of Neuroscience (LIM-27), Department and Institute of Psychiatry, Faculty of Medicine, University of Sao Paulo, SP, Brazil.
‡Department of Mental Health and National Institute of Science and Technology, Molecular Medicine, Faculty of Medicine, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
ACS Chem Neurosci. 2014 Jun 18;5(6):443-50. doi: 10.1021/cn5000309. Epub 2014 May 6.
Lithium is a well-established therapeutic option for the acute and long-term management of bipolar disorder and major depression. More recently, based on findings from translational research, lithium has also been regarded as a neuroprotective agent and a candidate drug for disease-modification in certain neurodegenerative disorders, namely, Alzheimer's disease (AD), amyotrophic lateral sclerosis (ALS), and, more recently, Parkinson's disease (PD). The putative neuroprotective effects of lithium rely on the fact that it modulates several homeostatic mechanisms involved in neurotrophic response, autophagy, oxidative stress, inflammation, and mitochondrial function. Such a wide range of intracellular responses may be secondary to two key effects, that is, the inhibition of glycogen synthase kinase-3 beta (GSK-3β) and inositol monophosphatase (IMP) by lithium. In the present review, we revisit the neurobiological properties of lithium in light of the available evidence of its neurotrophic and neuroprotective properties, and discuss the rationale for its use in the treatment and prevention of neurodegenerative diseases.
锂是双相情感障碍和重度抑郁症急性及长期治疗的一种成熟的治疗选择。最近,基于转化研究的结果,锂也被视为一种神经保护剂,以及某些神经退行性疾病(即阿尔茨海默病(AD)、肌萎缩侧索硬化症(ALS),以及最近发现的帕金森病(PD))疾病修饰的候选药物。锂的假定神经保护作用基于这样一个事实,即它调节参与神经营养反应、自噬、氧化应激、炎症和线粒体功能的几种稳态机制。如此广泛的细胞内反应可能继发于两个关键作用,即锂对糖原合酶激酶-3β(GSK-3β)和肌醇单磷酸酶(IMP)的抑制作用。在本综述中,我们根据锂的神经营养和神经保护特性的现有证据,重新审视锂的神经生物学特性,并讨论其用于治疗和预防神经退行性疾病的理论依据。