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作 者:苏岑[1] 张兴利[1] 黄韵如[1] 郑和鑫[1] 肖献忠[1] 曾庆仁[2] 谭斯品[1,2]
机构地区:[1]中南大学基础医学院,中国湖南长沙410078 [2]中南大学细胞与分子生物学实验教学中心,中国湖南长沙410083
出 处:《生命科学研究》2012年第4期319-323,共5页Life Science Research
基 金:中南大学学生潜质发掘专项项目(201011200090);湖南省自然科学基金资助项目(10JJ4016);教育部留学人员回国科研启动基金资助项目
摘 要:采用盲肠结扎穿孔(cecal ligation and puncture,CLP)法制备脓毒性休克大鼠模型,探讨血管活性肠肽(vasoactive intestinal peptide,VIP)对脓毒性休克大鼠肝损伤的保护作用及其可能机制.将48只雄性SD大鼠随机分成4组:假手术组(SO,n=12)、CLP组(n=12)、VIP组(n=12)和生理盐水组(NS,n=12).VIP组大鼠在行CLP术后即刻给予6 nmol VIP,应用酶联免疫吸附试验(ELISA)检测各组大鼠血清谷丙转氨酶ALT和谷草转氨酶AST水平,同时检测血清炎症因子:促炎因子肿瘤坏死因子-α(TNF-α),抑炎因子白介素-10(IL-10)的变化;取大鼠肝脏组织行病理检查.在6 h以后的各时间点,与NS组比较,VIP组TNF-α水平明显降低,IL-10水平持续升高,VIP组AST和ALT水平自12 h始明显降低,肝脏病理损伤明显改善.实验表明,VIP通过抑制促炎因子的生成并促进抗炎因子的产生在大鼠脓毒性休克肝损伤中发挥保护作用.Cecla ligation and puncture(CLP) was performed to produce septic shock rat model.Vasoactive intestinal peptide(VIP) was injected to investigate its protective effects on liver injury of septic shock rats and its possible mechanism.Forty-eight adult Sprague-dawley rats were randomly divided into 4 groups,with 12 animals in each group: sham operation group(SO group),CLP group,VIP group and normal Salin group(NS group).The rats in VIP group were given intravenous injection of VIP(6 nmol per art) instantly after the CLP operation.Enzyme-linked immunosorbent assays(ELASA) was performed to measure the serum con-centrations of alanine amiotransferase(ALT) and aspartate aminotransferase(AST),also the concentration of pro-inflammatory cytokines such as tumor necrosis factor(TNF-α),anti-inflammatory cytokines such as inter-leukin-10(IL-10) were measured.Rat liver was harvested for pathological examinations.At each time point after 6 h,in VIP group,the rat serum TNF-α concentration was decreased meanwhile IL-10 level was in-creased.After 12 h,ALT and AST concentration was decreased with markedly alleviated organ pathological injuries.Thus,it is proved that VIP exerts protective effects on liver injury of septic shock rats through in-hibiting production of proinflammatory factors and stimulating the production of anti-inflammatory cytokines.
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