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基于线粒体的脊髓损伤治疗方法:线粒体生物合成作为潜在的药理学靶点

Mitochondrial-Based Therapeutics for the Treatment of Spinal Cord Injury: Mitochondrial Biogenesis as a Potential Pharmacological Target.

作者信息

Scholpa Natalie E, Schnellmann Rick G

机构信息

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.)

出版信息

J Pharmacol Exp Ther. 2017 Dec;363(3):303-313. doi: 10.1124/jpet.117.244806. Epub 2017 Sep 21.

DOI:10.1124/jpet.117.244806
PMID:28935700
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5676296/
Abstract

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.

摘要

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。

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本文引用的文献

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Cardiovasc Diabetol. 2017 Feb 7;16(1):19. doi: 10.1186/s12933-017-0501-2.
2
Development of Therapeutics That Induce Mitochondrial Biogenesis for the Treatment of Acute and Chronic Degenerative Diseases.开发诱导线粒体生物合成用于治疗急慢性退行性疾病的疗法。
J Med Chem. 2016 Dec 8;59(23):10411-10434. doi: 10.1021/acs.jmedchem.6b00669. Epub 2016 Sep 27.
3
Inflammogenesis of Secondary Spinal Cord Injury.继发性脊髓损伤的炎症发生机制
Front Cell Neurosci. 2016 Apr 13;10:98. doi: 10.3389/fncel.2016.00098. eCollection 2016.
4
Lentivirus-mediated PGC-1α overexpression protects against traumatic spinal cord injury in rats.慢病毒介导的PGC-1α过表达可保护大鼠免受创伤性脊髓损伤。
Neuroscience. 2016 Jul 22;328:40-9. doi: 10.1016/j.neuroscience.2016.04.031. Epub 2016 Apr 27.
5
Effectiveness of minocycline and FK506 alone and in combination on enhanced behavioral and biochemical recovery from spinal cord injury in rats.米诺环素和FK506单独及联合使用对大鼠脊髓损伤后行为和生化恢复增强的有效性。
Pharmacol Biochem Behav. 2016 Jun;145:45-54. doi: 10.1016/j.pbb.2016.04.003. Epub 2016 Apr 19.
6
Synergistic Effects of Cilostazol and Probucol on ER Stress-Induced Hepatic Steatosis via Heme Oxygenase-1-Dependent Activation of Mitochondrial Biogenesis.西洛他唑和普罗布考通过血红素加氧酶-1依赖性激活线粒体生物合成对内质网应激诱导的肝脂肪变性的协同作用。
Oxid Med Cell Longev. 2016;2016:3949813. doi: 10.1155/2016/3949813. Epub 2016 Jan 6.
7
Time representation of mitochondrial morphology and function after acute spinal cord injury.急性脊髓损伤后线粒体形态和功能的时间表征
Neural Regen Res. 2016 Jan;11(1):137-43. doi: 10.4103/1673-5374.175061.
8
Mitochondrial division inhibitor 1 (Mdivi-1) offers neuroprotection through diminishing cell death and improving functional outcome in a mouse model of traumatic brain injury.线粒体分裂抑制剂1(Mdivi-1)通过减少细胞死亡和改善创伤性脑损伤小鼠模型的功能结局来提供神经保护作用。
Brain Res. 2016 Jan 1;1630:134-43. doi: 10.1016/j.brainres.2015.11.016. Epub 2015 Nov 17.
9
Mitochondrial Biogenesis as a Pharmacological Target: A New Approach to Acute and Chronic Diseases.线粒体生物发生作为药物靶点:急性和慢性疾病的新方法。
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BMC Genomics. 2015 Oct 20;16:822. doi: 10.1186/s12864-015-2054-7.