Scholpa Natalie E, Schnellmann Rick G
Department of Pharmacology and Toxicology, College of Pharmacy, University of Arizona, Tucson, Arizona (N.E.S., R.G.S.); and Southern Arizona VA Health Care System, Tucson, Arizona (R.G.S.).
Department of Pharmacology and Toxicology, College of Pharmacy, University of Arizona, Tucson, Arizona (N.E.S., R.G.S.); and Southern Arizona VA Health Care System, Tucson, Arizona (R.G.S.)
J Pharmacol Exp Ther. 2017 Dec;363(3):303-313. doi: 10.1124/jpet.117.244806. Epub 2017 Sep 21.
Spinal cord injury (SCI) is characterized by an initial trauma followed by a progressive cascade of damage referred to as secondary injury. A hallmark of secondary injury is vascular disruption leading to vasoconstriction and decreased oxygen delivery, which directly reduces the ability of mitochondria to maintain homeostasis and leads to loss of ATP-dependent cellular functions, calcium overload, excitotoxicity, and oxidative stress, further exacerbating injury. Restoration of mitochondria dysfunction during the acute phases of secondary injury after SCI represents a potentially effective therapeutic strategy. This review discusses the past and present pharmacological options for the treatment of SCI as well as current research on mitochondria-targeted approaches. Increased antioxidant activity, inhibition of the mitochondrial permeability transition, alternate energy sources, and manipulation of mitochondrial morphology are among the strategies under investigation. Unfortunately, many of these tactics address single aspects of mitochondrial dysfunction, ultimately proving largely ineffective. Therefore, this review also examines the unexplored therapeutic efficacy of pharmacological enhancement of mitochondrial biogenesis, which has the potential to more comprehensively improve mitochondrial function after SCI.
脊髓损伤(SCI)的特征是初始创伤后接着是一系列称为继发性损伤的渐进性损伤。继发性损伤的一个标志是血管破坏,导致血管收缩和氧气输送减少,这直接降低了线粒体维持内环境稳定的能力,并导致依赖ATP的细胞功能丧失、钙超载、兴奋性毒性和氧化应激,进一步加剧损伤。在脊髓损伤后继发性损伤的急性期恢复线粒体功能障碍是一种潜在有效的治疗策略。本综述讨论了过去和现在治疗脊髓损伤的药理学选择以及目前针对线粒体的研究方法。增加抗氧化活性、抑制线粒体通透性转换、替代能源以及操纵线粒体形态是正在研究的策略。不幸的是,这些策略中的许多都只解决了线粒体功能障碍的单个方面,最终证明大多无效。因此,本综述还研究了药物增强线粒体生物合成尚未探索的治疗效果,这有可能更全面地改善脊髓损伤后的线粒体功能。