Department of Emergency, Affiliated Hospital of Weifang Medical University, Weifang, Shandong 261031, P.R. China.
Department of Neurology Ⅱ, Affiliated Hospital of Weifang Medical University, Weifang, Shandong 261031, P.R. China.
Int J Med Sci. 2024 Jan 1;21(2):284-298. doi: 10.7150/ijms.88195. eCollection 2024.
Ischemic stroke ranks among the foremost clinical causes of mortality and disability, instigating neuronal degeneration, fatalities, and various sequelae. While standard treatments, such as intravenous thrombolysis and endovascular thrombectomy, prove effective, they come with limitations. Hence, there is a compelling need to develop neuroprotective agents capable of improving the functional outcomes of the nervous system. Numerous preclinical studies have demonstrated that lithium can act in multiple molecular pathways, including glycogen synthase kinase 3(GSK-3), the Wnt signaling pathway, the mitogen-activated protein kinase (MAPK)/ extracellular signal-regulated kinase (ERK) signaling pathway, brain-derived neurotrophic factor (BDNF), mammalian target of rapamycin (mTOR), and glutamate receptors. Through these pathways, lithium has been shown to affect inflammation, autophagy, apoptosis, ferroptosis, excitotoxicity, and other pathological processes, thereby improving central nervous system (CNS) damage caused by ischemic stroke. Despite these promising preclinical findings, the number of clinical trials exploring lithium's efficacy remains limited. Additional trials are imperative to thoroughly ascertain the effectiveness and safety of lithium in clinical settings. This review delineates the mechanisms underpinning lithium's neuroprotective capabilities in the context of ischemic stroke. It elucidates the intricate interplay between these mechanisms and sheds light on the involvement of mitochondrial dysfunction and inflammatory markers in the pathophysiology of ischemic stroke. Furthermore, the review offers directions for future research, thereby advancing the understanding of the potential therapeutic utility of lithium and establishing a theoretical foundation for its clinical application.
缺血性脑卒中是导致死亡和残疾的主要临床原因之一,可引发神经元变性、死亡和多种后遗症。尽管静脉溶栓和血管内取栓等标准治疗方法有效,但它们也存在局限性。因此,迫切需要开发能够改善神经系统功能预后的神经保护剂。大量临床前研究表明,锂可以作用于多个分子途径,包括糖原合酶激酶 3(GSK-3)、Wnt 信号通路、丝裂原活化蛋白激酶(MAPK)/细胞外信号调节激酶(ERK)信号通路、脑源性神经营养因子(BDNF)、哺乳动物雷帕霉素靶蛋白(mTOR)和谷氨酸受体。通过这些途径,锂已被证明可以影响炎症、自噬、细胞凋亡、铁死亡、兴奋性毒性和其他病理过程,从而改善缺血性脑卒中引起的中枢神经系统(CNS)损伤。尽管这些有前景的临床前发现,但探索锂疗效的临床试验数量仍然有限。需要更多的试验来彻底确定锂在临床环境中的有效性和安全性。本综述阐述了锂在缺血性脑卒中背景下的神经保护作用的机制。它阐明了这些机制之间的复杂相互作用,并揭示了线粒体功能障碍和炎症标志物在缺血性脑卒中病理生理学中的参与。此外,该综述为未来的研究提供了方向,从而加深了对锂潜在治疗用途的理解,并为其临床应用奠定了理论基础。