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Lithium and its neuroprotective and neurotrophic effects: potential treatment for post-ischemic stroke sequelae.

机译:锂及其神经保护和神经营养作用:缺血性中风后遗症的潜在治疗方法。

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Post-stroke cognitive impairment has a high prevalence in stroke patients and is associated with poor short and long term outcomes, including a negative impact on functional recovery. There is evidence that post-stroke impairment is the direct result of stroke induced neurological injury. Gray matter atrophy has been implicated in the development of post-stroke cognitive impairment and is the result of a series of neurochemical processes that are activated by ischemia. Lithium, traditionally used as a mood stabilizer, has been recognized in the last 10 years for its robust neuroprotective and neurotrophic effects against diverse insults, such as ischemia, both in vitro and in vivo. This has generated several preclinical and clinical studies of lithium treatment for managing neurodegenerative diseases and cerebral ischemia. Evidence suggests that lithium may protect against the cerebral atrophy and neuronal degeneration induced by the neurochemical processes and pathways known to regulate cell death and atrophy after an ischemic event. Lithium-mediated neurotroprotective and neurotrophic effects involve mechanisms highly relevant to the post-stroke population including the increased expression of brain-derived neurotrophic factor (BDNF) and Bcl-2, and inhibition of GSK-3beta. Lithium-induced increases in human gray matter have been reported and occur within a time frame consistent with the known effects of lithium through increased expression of BDNF, Bcl-2 and GSK-3beta inhibition. This article reviews the evidence to support the use of lithium to reduce neuronal damage post-stroke through 1) mechanisms of excitotoxicity and post-ischemic inflammation; and 2) neurotrophic signaling cascades. Lithium's relevant actions in preclinical and clinical studies will be reviewed and presented to support the neuroprotective and neurotrophic effects of lithium as well as other clinical considerations in using lithium in the post-ischemic stroke population.
机译:脑卒中后认知障碍在脑卒中患者中患病率很高,并与不良的短期和长期结果相关,包括对功能恢复的负面影响。有证据表明,中风后损伤是中风诱发的神经系统损伤的直接结果。灰质萎缩已与中风后认知功能障碍的发展有关,并且是由缺血激活的一系列神经化学过程的结果。传统上用作情绪稳定剂的锂在过去十年中因其对多种损伤(例如,体内和体外)的强大神经保护作用和神经营养作用而得到公认。这已经产生了用于治疗神经退行性疾病和脑缺血的锂治疗的一些临床前和临床研究。有证据表明,锂可能预防由缺血性事件后调节细胞死亡和萎缩的神经化学过程和途径引起的脑萎缩和神经元变性。锂介导的神经营养和神经营养作用涉及与中风后人群高度相关的机制,包括脑源性神经营养因子(BDNF)和Bcl-2的表达增加以及对GSK-3beta的抑制。锂诱导的人类灰质增加已经报道,并在一定的时间范围内发生,这与锂通过增加BDNF,Bcl-2和GSK-3beta抑制表达的已知作用一致。本文回顾了支持锂通过以下方法减少中风后神经元损害的证据:1)兴奋性毒性和缺血后炎症的机制; 2)神经营养信号级联。将对锂在临床前和临床研究中的相关作用进行回顾和介绍,以支持锂在缺血性中风后人群中使用锂的神经保护作用和神经营养作用以及其他临床考虑因素。

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