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[1]张立亚,崔尧丽,王 兵,等.z-VAD-FMK与Necrostatin-1联合对MODS大鼠器官的保护作用研究[J].天津医科大学学报,2014,20(02):85-088.
 ZHANG Li-ya,CUI Yao-li,WANG Bing,et al. Protective effect of z-VAD-FMK and Necrostatin-1 on the organs of rats with MODS[J].Journal of Tianjin Medical University,2014,20(02):85-088.
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z-VAD-FMK与Necrostatin-1联合对MODS大鼠器官的保护作用研究(PDF)
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《天津医科大学学报》[ISSN:1006-8147/CN:12-1259/R]

卷:
20卷
期数:
2014年02期
页码:
85-088
栏目:
基础医学
出版日期:
2014-03-20

文章信息/Info

Title:
 Protective effect of z-VAD-FMK and Necrostatin-1 on the organs of rats with MODS
文章编号:
1006-8147(2014)02-0085-04
作者:
张立亚1崔尧丽2王 兵2王勇强2王玉亮3
 (1.天津医科大学一中心临床学院,天津300192;2.天津市第一中心医院ICU,天津 300192;3.卫生部危重病急救医学重点实验室,天津 300384)
Author(s):
 ZHANG Li-ya1 CUI Yao-li2 WANG Bing2 WANG Yong-qiang2 WANG Yu-liang3
 (1. Clinical Medicine College, First Central Hospital, Tianjin Medical University, Tianjin 300192, China; 2. Intensive Medicine, Tianjin First Center Hospital, Tianjin 300192, China; 3. Key Laboratory of the Ministry of Health of Critical Care Emergency Medicine, Tianjin 300384, China)
关键词:
多器官功能障碍综合征z-VAD-FMKNecrostatin-1大鼠
Keywords:
 MODS z-VAD-FMK Necrostatin-1 rat
分类号:
R36
DOI:
-
文献标志码:
A
摘要:
 目的: 探讨z-VAD-FMK与Necrostatin-1联合对MODS大鼠器官的保护作用。 方法: 采用失血性休克-内毒素“二次打击”建立大鼠MODS动物模型。将80只雄性SD大鼠随机分为4组:z-VAD-FMK组、Nec-1组、z-VAD-FMK+Nec-1组、模型组,每组20只,观察72 h死亡率。另取40只雄性SD大鼠随机分为5组:假手术组、z-VAD-FMK组、Nec-1组、z-VAD-FMK+Nec-1组、模型组,每组8只,分别于注射内毒素和生理盐水后24 h收集血清和肝、肺、肠组织。全自动生化仪检测血清ALT、AST的变化,血气分析仪检测PaO2的变化,双抗体夹心酶联免疫法检测血清TNF-α、IL-β的变化,HE染色观察肝、肺、肠组织的病理学改变。 结果 : 大鼠遭受失血性休克-内毒素“二次打击”后,血清ALT、AST明显升高(P < 0.01),动脉氧分压PaO2显著下降(P < 0.01),血清炎性因子TNF-α、IL-1β水平明显升高(P < 0.01),光镜下见肝窦明显扩张、淤血,肝小叶结构紊乱,肝细胞部分变性、坏死;肺泡壁结构被破坏、肺间质充血、大量炎性细胞浸润;肠绒毛结构被破坏、部分绒毛顶部细胞、隐窝细胞变性、坏死,大量炎性细胞浸润。而z-VAD-FMK组、Nec-1组及z-VAD-FMK+Nec-1组ALT、AST升高程度、PaO2下降程度、TNF-α、IL-1β升高程度均显著低于模型组(P < 0.01),以z-VAD-FMK+Nec-1组变化最明显。72 h死亡率均较模型组显著降低(P < 0.05)。结论 : z-VAD-FMK、Nec-1、z-VAD-FMK+Nec-1联合治疗均可显著减轻MODS大鼠的器官损伤,联合治疗效果更佳。
Abstract:
Objective: To investigate the protective effect of z-VAD-FMK and Necrostatin-1 on the organs of rats with MODS. Methods: Adult male SD rats were used and rat model was produced by hemorrhagic shock based on injecting LPS. A total of 80 rats were randomly divided into four groups: z-VAD-FMK group; Nec-1 group; z-VAD-FMK+Nec-1 group, with 20 rats in each group. And the 72 h mortality was observed. In addition, other 40 rats were randomly divided into five groups: sham group; z-VAD-FMK group; Nec-1 group; z-VAD-FMK+Nec-1 group; model group, with 8 rats in each group. The samples of different groups were collected at 24 h after injecting LPS or normal saline. Serum ALT and AST were detected by automatic biochemistry analyzer. PaO2 was detected by blood gas analyzer. And serum TNF-αand IL-βwere detected by ELISA. The pathological changes of liver, lung and intestine were observed by H&E staining. Results: After hemorrhagic shock, the expression of ALT, AST, TNF-αand IL-β significantly increased (P < 0.01) while the level of PaO2 markedly reduced (P < 0.01). Under light microscopy, hepatic sinus expansion, liver cells degeneration, necrosis, as well as infiltration of abundant inflammatory cells were observed; the structure of alveolar walls were destroyed and the pulmonary interstitial hyperemia and infiltration of abundant inflammatory cells were observed; the structure of intestinal villi were destroyed and the top part of villi cells and crypt cells degeneration, necrosis, as well as infiltration of abundant inflammatory cells were observed. Compared with model group, the up-regulation degree of ALT, AST, TNF-αand IL-βand the PaO2 reductionwere smaller in z-VAD-FMK group, Nec-1 group and z-VAD-FMK+Nec-1 group (P < 0.01). And the changes in z-VAD-FMK+Nec-1 group were the most significant. In addition, the 72 h mortality significantly reduced (P < 0.05). Conclusion: The z-VAD-FMK, Nec-1 and z-VAD-FMK+Nec-1 can significantly reduce the organ damage of rats with MODS, and combining z-VAD-FMK and Nec-1 can bring marked results.

参考文献/References:

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备注/Memo

备注/Memo:
基金项目 国家临床重点专科建设经费及国家自然科学基金资助项目(81301624)
作者简介 张立亚(1988-),女,硕士在读,研究方向:多器官功能障碍综合征发病机制研究; 通信作者:王勇强,E-mail:yongqiangwang1962@sina.com。
更新日期/Last Update: 2014-03-30