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甘草酸二铵对脊髓缺血再灌注损伤后IL-4/IL-8/TNF-α表达的影响 被引量:1

Effects of diammonium glycyrrhizinate on expression of IL-4/IL-8/TNF-α in rats with spinal cord ischemia-reperfusion injury
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摘要 目的初步探讨甘草酸二铵(Diammonium Glycyrrhizinate,DG)对脊髓缺血再灌注损伤后脊髓组织中炎性细胞因子IL-4、IL-8、TNF-α表达的影响。方法雄性SD大鼠90只,随机分为空白对照组、阴性对照组、DG干预组三组,通过外科手术法造成大鼠腰段脊髓的缺血再灌注损伤,组织匀浆后采用ELISA检测IL-4、IL-8、TNF-α的表达。结果与阴性对照组比较:空白对照组IL-4在24、72、168h有统计学意义(P<0.05),DG干预组IL-4在3、24h时间段有统计学意义(P<0.05);阴性对照组IL-8各时间段均有统计学意义(P<0.05);DG干预组IL-824、72h时间段有统计学意义(P<0.05);空白对照组TNF-α各时间段均有统计学意义(P<0.05);DG干预组TNF-α全部时间段均有统计学意义(P<0.05)。结论脊髓缺血再灌注损伤后IL-4、IL-8、TNF-α的表达明显发生变化,DG可能通过影响IL-4、IL-8、TNF-α的表达发挥保护作用。 Objective To evaluate effects of diammonium glycyrrhiryzinate on ischemia-reperfusion injury of spinal cord and it's influence on the expression of IL-4,IL-8 as well as TNF-α in spinal cord tissue.Methods Ninety male Sprauge-Dawley rats were randomly divided into the control group(n=10),negative control group(n=40)and DG intervention group(n=40).The spinal cord ischemia-reperfusion model was established by surge method and assay the TNF-α,IL-4,IL-8 levels by ELISA.Results Comparing with the blank group,the IL-4 of negative control group at 24h,72h,168h time period was significantly different(P0.05),and the DG intervention group in 3h,24h was significantly different(P0.05);The IL-8 of negative control was significantly different in each period(P0.05),and the IL-8 of DG intervention group was significant different at 24h and 72h time period(P0.05);The TNF-a of negative control group was significantly different at each time section(P0.05),and the DG intervention group were significant different at all the time(P0.05).Conclusion Significant changes with regard to the expression of IL-4,IL-8 and TNF-α in lumbar spinal cord is found after ischemia-reperfusion injury,and DG may protect the spinal cord by influencing the IL-4,IL-8,TNF-αexpression.
出处 《宁夏医学杂志》 CAS 2010年第6期510-512,共3页 Ningxia Medical Journal
基金 银川市科技攻关资助项目(2008053)
关键词 甘草酸二铵 脊髓缺血再灌注损伤 炎性因子 Diammonium glycyrrhizinate Spinal cord ischemia-reperfusion Inflammatory cytokines
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