肠缺血/再灌注损伤后白介素1-β水平与磷脂酶A2激活的关系

 
 


颜光涛
*,  郝秀华, 薛辉, 王录焕, 李英丽, 石丽萍
(
解放军总医院基础医学研究所生物化学研究室,北京 100853)

 
 

 

 
 

摘 要:
为了探讨肠缺血/再灌注损伤后IL-1β基因表达和蛋白含量变化与磷脂酶A2抑制之间的关系,采用大鼠肠缺血/再灌注损伤模型, 在对照组、损伤组和磷脂酶A2抑制剂处理组动物中收集血清、肺灌洗液、腹腔灌洗液及全身重要脏器组织样品, 采用放射免疫法测定IL-1β含量, 并用RT-PCR法测定肺组织中IL-1β和Ⅱ型PLA2基因表达。结果表明, 损伤后6 h血清中IL-1β含量明显高于对照组;损伤后13 h, 腹腔液中IL-1β也明显高于对照组;损伤后肝组织中IL-1β水平有明显增加,而肺、肾、肠组织中IL-1β没有明显变化。损伤后肺灌洗液中IL-1β也明显高于对照组水平, 肺组织中IL-1β mRNA表达增加, 而Ⅱ型PLA2 mRNA在损伤后表达反而有所下降。采用磷脂酶A2抑制剂氯喹、环氧化物酶抑制剂消炎痛、血小板活化因子受体阻断剂SR27417, IL-1β蛋白和基因表达有不同的改变。提示肠缺血/再灌注损伤后一定时间内, 肝内IL-1β    mRNA表达和血中IL-1β水平明显增高, 但是否与磷脂酶A2激活或其代谢产物的释放有关尚需进一步证明。

关键词: 
肠缺血/再灌注损伤; 白介素-1β; 磷脂酶A2
学科分类号:
Q593; R392-33

 
 

 

 

Interleukin-1β  expression and phospholipase A2 activation after intestinal  ischemia/reperfusion injury

 


YAN Guang-Tao, HAO Xiu-Hua, XUE Hui, WANG Lu-Huan, LI Ying-LI, SHI Li-Ping
(Laboratory of Biochemistry, Basic Medicine Institute, General Hospital of PLA, Beijing 100853)

 


Abstract: 
The experiments were carried out to explore the interactions between IL-1 beta gene expression, protein level and phospholipase A2 PLA2 inhibition after intestinal ischemia/reperfusion injury. Using a rat intestinal ischemia/reperfusion injury model, after collecting the serum, lung lavage, abdomen cavity lavage and important organ tissue samples from control, injury and PLA2 inhibitor treated groups, IL-1 beta level was measured by radioimmunoassay,  and the mRNA expression of IL-1beta and type PLA2 was determined by RT-PCR. After 6 hours of injury the IL-1 beta level in serum  was significantly higher than that in the control group; an increase in IL-1 beta was also observed in abdomen cavity lavage  1 or 3 hours after injury. IL-1 beta was significantly increased in liver tissue after injury, but was not changed obviously in the lung, kidney and intestinal tissues. IL-1 beta in the lung lavage was significantly higher than that of control group. The mRNA expression of IL-1beta in lung tissue was increased after injury, but type PLA2 mRNA expression was decreased. There were different changes in IL-1 beta level and gene expression after treatments with PLA2 inhibitor chloroquine, cyclo-oxidase inhibitor indomethacin, or PAF receptor antagonist SR27417 respectively  after injury. All these results indicate that after intestinal ischemia/ reperfusion injury, the IL-1 beta level and mRNA gene expression are significantly increased, however, the relationship among  IL-1 beta,  PLA2  activation and its metabolites releases remains to be further elucidated.

Key words:
intestinal ischemia/reperfusion injury; interleukin-1beta; phospholipase A2
 

     
     
 

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