Department of Hand and Foot Surgery, The Second Hospital of Jilin University, Changchun, 130012, China.
Institute of Stem Cells and Regenerative Medicine, Department of Physiology, Guangdong Medical University, Dongguan, 523808, China.
Biochem Biophys Res Commun. 2019 Jan 22;508(4):1126-1132. doi: 10.1016/j.bbrc.2018.11.124. Epub 2018 Dec 12.
Brachial plexus root avulsion causes severe sequelae Treatments and prognosis face many problems, including inflammatory reaction, oxidative damage, and myelin related inhibitory effect. l-Theanine has anti-inflammatory, anti-oxidative, and neuroprotective effects. NEP1-40 competitively inhibits Nogo-66 receptor (NgR1) promotes axonal regeneration. Forty-eight Sprague-Dawley rats were randomly assigned into four groups to establish an animal model of brachial plexus root avulsion. Inflammation and oxidative damage were evaluated by spectrophotometry and motor function of the upper limbs was assessed via Terzis grooming test after modeling. Immunofluorescence and hematoxylin and eosin staining were utilized to determine the content of reactive oxygen species, activation of microglial cells, neuroprotection, and nerve regeneration. Compared with the control group, the L-Theanine + NEP1-40 group had significantly decreased myeloperoxidase, malondialdehyde, interleukin-6, reactive oxygen species, and microglial cells, significantly increased score on the Terzis grooming test, increased motor neuron content, and thickened muscle fibers, increased area, and appearance of large and clear motor endplate structures. The results of this study suggest that l-Theanine combined with NEP1-40significantly promoted nerve regeneration after brachial plexus root avulsion, and may be a potential treatment for promoting nerve regeneration. Possible mechanisms underlying these results are alleviation of oxidative damage and inflammatory responses in the injured area and antagonism of myelin inhibition.
臂丛神经根撕脱伤导致严重后遗症,治疗和预后面临诸多问题,包括炎症反应、氧化损伤和髓鞘相关抑制作用。茶氨酸具有抗炎、抗氧化和神经保护作用。NEP1-40 竞争性抑制 Nogo-66 受体(NgR1),促进轴突再生。将 48 只 Sprague-Dawley 大鼠随机分为四组,建立臂丛神经根撕脱伤动物模型。建模后,通过分光光度法评估炎症和氧化损伤,通过 Terzis 梳理试验评估上肢运动功能。免疫荧光和苏木精-伊红染色用于测定活性氧含量、小胶质细胞激活、神经保护和神经再生。与对照组相比,茶氨酸+NEP1-40 组髓过氧化物酶、丙二醛、白细胞介素-6、活性氧和小胶质细胞明显减少,Terzis 梳理试验评分明显升高,运动神经元含量增加,肌纤维增粗,面积增大,大而清晰的运动终板结构外观。本研究结果表明,茶氨酸联合 NEP1-40 可显著促进臂丛神经根撕脱伤后的神经再生,可能是促进神经再生的一种潜在治疗方法。其结果的可能机制是减轻损伤部位的氧化损伤和炎症反应,以及拮抗髓鞘抑制。