Tabassum Sidra, Wu Silin, Lee Chang-Hun, Yang Bosco Seong Kyu, Gusdon Aaron M, Choi Huimahn A, Ren Xuefang S
Novel Treatments for Acute Brain Injury Institute, Texas Medical Center, TX, USA; Department of Neurosurgery, McGovern Medical School, University of Texas Health Science Center, Houston, TX, USA.
Department of New Biology, Daegu Gyeongbuk Institute of Science and Technology, Daegu, Republic of Korea.
Neurotherapeutics. 2025 Jan;22(1):e00515. doi: 10.1016/j.neurot.2024.e00515. Epub 2024 Dec 24.
Traumatic brain injury (TBI) is a leading cause of morbidity and mortality worldwide, with limited effective therapeutic options currently available. Recent research has highlighted the pivotal role of mitochondrial dysfunction in the pathophysiology of TBI, making mitochondria an attractive target for therapeutic intervention. This review comprehensively examines advancements in mitochondrial-targeted therapies for TBI, bridging the gap from basic research to clinical applications. We discuss the underlying mechanisms of mitochondrial damage in TBI, including oxidative stress, impaired bioenergetics, mitochondrial dynamics, and apoptotic pathways. Furthermore, we highlight the complex interplay between mitochondrial dysfunction, inflammation, and blood-brain barrier (BBB) integrity, elucidating how these interactions exacerbate injury and impede recovery. We also evaluate various preclinical studies exploring pharmacological agents, gene therapy, and novel drug delivery systems designed to protect and restore mitochondrial function. Clinical trials and their outcomes are assessed to evaluate the translational potential of mitochondrial-targeted therapies in TBI. By integrating findings from bench to bedside, this review emphasizes promising therapeutic avenues and addresses remaining challenges. It also provides guidance for future research to pave the way for innovative treatments that improve patient outcomes in TBI.
创伤性脑损伤(TBI)是全球发病和死亡的主要原因,目前有效的治疗选择有限。最近的研究强调了线粒体功能障碍在TBI病理生理学中的关键作用,使线粒体成为治疗干预的一个有吸引力的靶点。这篇综述全面审视了针对TBI的线粒体靶向治疗的进展,弥合了从基础研究到临床应用的差距。我们讨论了TBI中线粒体损伤的潜在机制,包括氧化应激、生物能量学受损、线粒体动力学和凋亡途径。此外,我们强调了线粒体功能障碍、炎症和血脑屏障(BBB)完整性之间的复杂相互作用,阐明了这些相互作用如何加剧损伤并阻碍恢复。我们还评估了各种临床前研究,这些研究探索了旨在保护和恢复线粒体功能的药物制剂、基因治疗和新型药物递送系统。评估临床试验及其结果,以评估线粒体靶向治疗在TBI中的转化潜力。通过整合从实验室到床边的研究结果,这篇综述强调了有前景的治疗途径并解决了剩余的挑战。它还为未来的研究提供指导,为改善TBI患者预后的创新治疗铺平道路。