期刊文献+

匹立尼酸对肝脏缺血-再灌注大鼠血清TNF-α和IL-1β的影响

Effects of pirinixic acid on serum TNF-α and IL-1β in rats with hepatic ischemia-reperfusion injury
下载PDF
导出
摘要 目的观察匹立尼酸(Wy14643)对肝脏缺血-再灌注大鼠血清肿瘤坏死因子α(TNF-α)和白细胞介素1β(IL-1β)的影响。方法SD雄性大鼠30只,体重220-280g,随机均分为五组:W1、W2、W2组、缺血-再灌注组(LR组)和假手术组(S组)。阻断左、中侧肝动脉及其门静脉(缺血约70%)90min后再灌注建立大鼠缺血-再灌注模型,S组操作同前但不阻断血管。缺血前1h,W1、W2、W3组分别经腹腔注射Wy146431、5、10mg/kg,I-R组和S组注射等容积生理盐水。4h后取腹主动脉血测定血清TNF-α和IL-1β水平。结果再灌注4h后,S组血清TNPα和IL-1β水平明显低于其它四组(P〈0.05);W2、W3组明显低于LR组(P〈0.05)。结论预先给予匹立尼酸可降低肝脏缺血一再灌注后血清TNF-α和IL-1β水平。 Objective To observe the effects of pirinixic acid (Wy14643) on serum TNF-α and IL-1β in rats with hepatic ischemia-reperfusion (I-R) injury. Methods Thirty male Sprague-Dawley rats weighing 220-280 g were equally randomized into five groups: Wy14643 1 mg/kg + I R group (group W1 ), Wy14643 5 mg/kg + I-R group (group W2), Wy14643 10 mg/kg +I-R group (group W3), sham operation group (group S) and I-R group (group I-R). Hepatic I-R injury model was established by clamping blood supply of the left and median lobes of the liver with vascular clamps for 90 min. Rats in group S were done the same operation without clamping blood vessels. Rats in groups W1, W2 and W3 were intraperitoneally administered with the dose of Wy14643 1, 5 and 10 mg/kg 60 min before ischemia, respectively. In groups S and I-R, rats were given the same volume of saline at the same time. Blood samples were taken from abdominal aorta 4 h after reperfusion to measure the serum levels of TNF-α and IL-1β. Results Four hours after hepatic I-R, group S had lower serum TNF-α and IL-1β compared with groups W1 , W2, W3 and I-R (P〈0. 05). Groups W2 and W3 had lower serum TNF-αand IL-1βcompared with group I-R (P〈0. 05). Conclusion Pretreatment with pirinixic acid can reduce the serum levels of TNF-α and IL-1β in rats with hepatic ischemia-reperfusion injury.
出处 《临床麻醉学杂志》 CAS CSCD 北大核心 2011年第9期916-918,共3页 Journal of Clinical Anesthesiology
关键词 匹立尼酸 肝脏 缺血-再灌注 肿瘤坏死因子Α 白细胞介素1Β Pirinixic acid Liver Ischemia reperfusion TNF -α IL -1β
  • 相关文献

参考文献7

  • 1Kleemann R, Verschuren L, de Rooij BJ, et al. Evidence for anti inflammatory activity of stalins and PPARalpha activators in hu- man C-reactive protein transgenic mice in vivo and in cultured hu- man hepatocytes in vitro. Blood, 2004,103:4188-4194.
  • 2Okaya T, Lentsch AB. Peroxisome proliferator-acivated re- ceptor-alpha regulates postischemic liver injury. Am J Physiol Gastrointest Liver Physiol, 2004, 286:G606-G612.
  • 3吴瑶,刘存明,朱敬明,王忠云,董世阳,张国楼.肝脏缺血-再灌注2相损伤对胰岛β细胞分泌功能的影响[J].临床麻醉学杂志,2009,25(3):252-254. 被引量:6
  • 4Staumont-Salle D, Abboud G, Brenuchon C, et al. Peroxi- some proliferator-activated receptor alpha regulates skin in -flammation and humoral response in atopic dermatitis. J Aller- gy Clin Immunol,2008, 121:962- 968.
  • 5Zambon A, Gervois P, Pauletto P, et al. Modulation of hepat- ic inflammatory risk markers of cardiovascular diseases by PPAR alpha activators: clinical and experimental evidence. Ar- terioscler Thromb Vasc Biol, 2006, 26 : 977- 986.
  • 6Stienstra R, Mandard S, Tan NS, et al. The Interleukin-1 re- ceptor antagonist is a direct target gene of PPARalpha in liver. J Hepatol,2007, 46: 869 -877.
  • 7Cuzzocrea S,Di Paola R, Mazzon E, et al. WY 14643. a po- tent exogenous PPAR -alpha ligand, reduces intestinal injury associated with splanchnic artery occlusion shock. Shock, 2004, 22:340 -346.

二级参考文献11

共引文献5

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部