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急性脊髓损伤模型大鼠与白细胞介素1受体拮抗剂的保护作用
作者姓名:黄颉刚  宗少晖  欧 超  熊春翔  赵玉玺
作者单位:广西医科大学,微生物学教研室,第一附属医院脊柱骨病外科,医学科学实验中心,广西壮族自治区南宁市 530021
基金项目:课题由广西医科大学博士启动基金(308010)及广西教育厅科研基金(桂教200710LX063)资助,名称:白细胞介素1受体拮抗剂对急性脊髓损伤的组织学研究。
摘    要:背景:白细胞介素1受体拮抗剂对大鼠急性脊髓损伤后脊髓功能修复具有保护作用,但具体机制不明。 目的:观察白细胞介素1受体拮抗剂对大鼠急性脊髓损伤组织神经丝蛋白质200和胶质纤维酸性蛋白的影响。 方法:SD大鼠随机分成假手术组,生理盐水对照组和白细胞介素1受体拮抗剂治疗组。采用改良Allen氏打击法建立急性脊髓损伤大鼠模型。分别在建模后1,48和72 h获取损伤段8 mm脊髓标本。 结果和结论:免疫组织化学染色检测,白细胞介素1受体拮抗剂治疗组神经丝蛋白质200和胶质纤维酸性蛋白的表达较假手术组和生理盐水组高,差异有显著性意义(P < 0.05)。提示白细胞介素1受体拮抗剂可使急性脊髓损伤大鼠模型损伤段脊髓神经丝蛋白质200和胶质纤维酸性蛋白表达增加,对急性脊髓损伤发挥保护作用。

关 键 词:急性脊髓损伤  白细胞介素1受体拮抗剂  神经丝蛋白质200  胶质纤维酸性蛋白  炎症反应  
收稿时间:2011-04-20

Effect of interleukin-1 receptor antagonist on neurofilament protein 200 and glial fibrillary acidic protein expression in a rat model of acute spinal cord injury
Authors:Huang Jie-gang  Zong Shao-hui  Ou Chao  Xiong Chun-xiang  Zhao Yu-xi
Institution:Department of Microbiology, Department of Spine Surgery, First Affiliated Hospital of Guangxi Medical University, Central Laboratory of Medical Sciences, Guangxi Medical University Nanning   530021, Guangxi Zhuang Autonomous Region, China
Abstract:BACKGROUND: Interleukin-1 receptor shows protective effects on spinal cord function recovery in rats with acute spinal cord injury, but the precise mechanism remains poorly understood. OBJECTIVE:To investigate the effect of interleukin-1 receptor antagonist (IL-1Ra) on neurofilament protein 200 (NF 200) and glial fibrillary acidic protein (GFAP) expression in rat acute spinal cord injury tissue. METHODS:A total of 90 Sprague-Dawley rats were randomly divided into three groups: sham-operated, normal saline and IL-1Ra treatment group. Acute spinal cord injury models were established by improved Allen’s method. At 1, 48 and 72 hours after model establishment, an 8-mm spinal cord segment was dissected longitudinally from the lesion site in each group. The NF200 and GFAP expression was detected by immunohistochemical staining. RESULTS AND CONCLUSION: NF200 and GFAP expression in the IL-1Ra trentment group was significantly higher than that in the sham-operated and normal saline group (P < 0.05). These results showed that IL-1Ra can increase NF200 and GFAP expression in the injured spinal cord segment and exhibit protective effect on acute spinal cord injury.
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