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Dual Regeneration of Muscle and Nerve by Intramuscular Infusion of Mitochondria in a Nerve Crush Injury Model

去神经支配 坐骨神经 线粒体 肌肉萎缩 医学 萎缩 腓肠肌 心肌细胞 神经损伤 MFN2型 解剖 内科学 内分泌学 麻醉 骨骼肌 化学 细胞生物学 生物 线粒体融合 线粒体DNA 生物化学 基因
作者
Meei‐Ling Sheu,Chiung‐Chyi Shen,Hsi‐Kai Tsou,Meng Yang,Hong‐Lin Su,Jason P. Sheehan,Ming‐Hong Chang,Hong-Shiu Chen,Hung-Chuan Pan
出处
期刊:Neurosurgery [Lippincott Williams & Wilkins]
卷期号:89 (1): E49-E59 被引量:7
标识
DOI:10.1093/neuros/nyab105
摘要

Peripheral nerve injuries result in muscle denervation and apoptosis of the involved muscle, which subsequently reduces mitochondrial content and causes muscle atrophy. The local injection of mitochondria has been suggested as a useful tool for restoring the function of injured nerves or the brain.To determine outcomes following the administration of isolated mitochondria into denervated muscle after nerve injury that have not been investigated.Muscle denervation was conducted in a sciatic nerve crushed by a vessel clamp and the denervated gastrocnemius muscle was subjected to 195 μg hamster green fluorescent protein (GFP)-mitochondria intramuscular infusion for 10 min.The mitochondria were homogeneously distributed throughout the denervated muscle after intramuscular infusion. The increases in caspase 3, 8-oxo-dG, Bad, Bax, and ratio of Bax/Bcl-2 levels in the denervated muscle were attenuated by mitochondrial infusion, and the downregulation of Bcl-2 expression was prevented by mitochondrial infusion. In addition, the decrease in the expression of desmin and the acetylcholine receptor was counteracted by mitochondrial infusion; this effect paralleled the amount of distributed mitochondria. The restoration of the morphology of injured muscles and nerves was augmented by the local infusion of mitochondria. Mitochondrial infusion also led to improvements in sciatic functional indexes, compound muscle action potential amplitudes, and conduction latencies as well as the parameters of CatWalk (Noldus) gait analysis.The local infusion of mitochondria can successfully prevent denervated muscle atrophy and augment nerve regeneration by reducing oxidative stress in denervated muscle.
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