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补阳还五汤对脊髓损伤后Ⅰ型胶原蛋白和Ⅳ型胶原蛋白表达的影响 被引量:16

Effects of Buyang Huanwu decoction on the expression of collagen type Ⅰ and Ⅳ after spinal cord injury
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摘要 背景:研究表明,Ⅰ型胶原蛋白和Ⅳ型胶原蛋白有利于脊髓损伤后肢体运动功能的恢复。目的:通过观察脊髓损伤大鼠肢体运动功能变化及Ⅰ型胶原蛋白和Ⅳ型胶原蛋白的表达,探讨补阳还五汤对脊髓损伤后大鼠肢体运动功能改善的可能机制。方法:实验方案经福建中医药大学动物实验伦理委员会批准[批准号为SYXK(闽)2013-005]。将54只大鼠随机分为3组:假手组(n=18)、模型组(n=18)和补阳还五汤组(n=18)。假手术组切除椎板后立即缝合伤口,其余2组切除椎板后应用NYU脊髓打击器建立脊髓损伤模型。造模后第1天开始补阳还五汤组给予补阳还五汤1 mL灌胃,模型组和假手术组术后蒸馏水1 mL灌胃。干预后1,3,5,7 d对各组大鼠进行BBB肢体运动功能评分;干预7 d后取材,尼式染色观察脊髓神经元形态和免疫组织化学检测Ⅰ型胶原蛋白和Ⅳ型胶原蛋白表达;电镜观察脊髓髓鞘超微结构,Western blot检测Ⅰ型胶原蛋白和Ⅳ型胶原蛋白的蛋白表达量。结果与结论:(1)干预第5天后,补阳还五汤组的BBB肢体运动功能评分显著高于同期的模型组(P <0.05);(2)尼式染色显示补阳还五汤组的细胞形态较为完整,细胞水肿较轻,瘀血面积较小,神经元恢复情况好于模型组;(3)电镜实验发现补阳还五汤组的髓鞘形态较模型组完整,水肿情况较轻,与尼式染色结果一致;(4)免疫组织化学显示补阳还五汤组的Ⅰ型胶原蛋白和Ⅳ型胶原蛋白的表达量均较模型组显著增多(P <0.05);(5)Western blot显示补阳还五汤组的Ⅰ型胶原蛋白和Ⅳ型胶原蛋白的表达量均较模型组显著增多(P <0.05);(6)结果说明,补阳还五汤能够改善脊髓损伤后大鼠的肢体运动功能障碍,其机制可能与增加Ⅰ型胶原蛋白和Ⅳ型胶原蛋白表达有关。 BACKGROUND: Collagen type I and IV are shown to be beneficial for limb locomotion recovery after spinal cord injury.OBJECTIVE: To explore the mechanism of Buyang Huanwu decoction on the rehabilitation of limb locomotion of rats after spinal cord injury by observing the changes of limb locomotion and expression levels of collagen type I and IV.METHODS: The study was approved by the Experimental Animal Ethics Committee of Fujian University of Traditional Chinese Medicine,approval number: SYXK2013-005. Fifty-four Sprague-Dawley rats were divided into three groups, sham, model and Buyang Huanwu decoction groups(n=18/group). Rats in the sham group underwent the laminectomy and rats in the other groups were used for establishing the spinal cord injury model by NYU impactor. The rats in the Buyang Huanwu decoction group, and sham and model groups were administrated 1 mL of Buyang Huanwu decoction and normal saline via gavage, respectively, at 1 day post-injury. Basso, Beattie, and Bresnahan limb locomotion scores were evaluated at 1, 3, 5 and 7 days after injury. At 7 days after injury, samples were removed for Nissl staining to observe the morphology of spinal cord neurons and the expression levels of collagen type I and IV were detected by immunohistochemistry. The ultrastructures of medullary sheath were observed under transmission electron microscope. The expression levels of collagen type I and IV proteins were detected by western blot assay.RESULTS AND CONCLUSION:(1) The Basso, Beattie, and Bresnahan limb locomotion scores from the fifth day after modeling in the Buyang Huanwu decoction group were significantly higher than those in the model group(P < 0.05).(2) Nissl staining showed that in the Buyang Huanwu decoction group, the structure of neurons was complete, cell edema was slight, hemostasis area was small, and the recovery of neurons was better than that in the model group.(3) Transmission electron microscope showed that the structure of myelin sheath in the Buyang Huanwu decoction group was better than that in the model group, and with slight edema, which were similar with the Nissl staining results.(4) Immunohistochemistry results showed that the expression levels of collagen type I and IV in the Buyang Huanwu decoction group were significantly higher than those in the model group(P < 0.05).(5) Western blot assay results showed that expressions of collagen type I and IV proteins in the Buyang Huanwu decoction group were significantly higher than those in the model group(P < 0.05).(6) In summary,Buyang Huanwu decoction can promote the rehabilitation of limb locomotion of rats after spinal cord injury, possibly by up-regulating the expressions of collagen type I and IV.
作者 林晓敏 潘伟滨 吴玉琼 范筱 Lin Xiaomin;Pan Weibin;Wu Yuqiong;Fan Xiao(Zhangzhou Health Vocational College,Zhangzhou 363000,Fujian Province,China;Qingdao Municipal Hospital,Qingdao 266000,Shandong Province,China)
出处 《中国组织工程研究》 CAS 北大核心 2019年第31期4986-4991,共6页 Chinese Journal of Tissue Engineering Research
基金 福建省中青年教师教育科研社科项目(社科)(JAS161084),项目负责人:潘伟滨~~
关键词 脊髓损伤 补阳还五汤 Ⅰ型胶原蛋白 Ⅳ型胶原蛋白 髓鞘 超微结构 spinal cord injury Buyang Huanwu decoction collagen type Ⅰ collagen type Ⅳ medullary sheath ultrastructure
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