期刊文献+

异丙酚对大鼠失血性休克复苏后肠道的保护作用 被引量:5

Protective Effect of Propofol on Intestine after Hemorrhagic Shock and Resuscitation
下载PDF
导出
摘要 目的:探讨短时间内异丙酚对失血性休克复苏后肠道的保护作用。方法:将大鼠随机分为假手术组(C组)、失血性休克复苏组(HS-R组)和异丙酚组(P组),每组8只。建立失血性休克复苏动物模型,HS-R组、P组分别在复苏后采用微量泵持续泵入生理盐水1mL·kg-1·h-1、异丙酚1mL·kg-1·h-1,维持2h,测血浆中二胺氧化酶(DAO)水平;开腹取小肠组织约5cm,3cm匀浆后分别采用黄嘌呤氧化酶法、硫代巴比妥酸比色法测超氧化物歧化酶(SOD)和丙二醛(MDA)水平,2cm做病理组织切片HE染色,观察肠道组织病理学改变。结果:HS-R组及P组的MDA及DAO水平均较C组升高,P组较HS-R组有所降低(均P<0.05);HS-R组及P组的SOD水平较C组降低,P组较HS-R组有所升高(均P<0.05);肠道组织病理学评分P组及HS-R组均高于C组,但P组较HS-R组低(均P<0.05)。结论:失血性休克复苏后肠道组织出现明显的损伤,短时间内异丙酚可通过抗氧自由基作用减轻此损伤。 Objective: To determine the protective effect of propofol on intestine after hemorrhagic shock and resuscitation in rats when used for a short period of time. Methods: Thirty Wistar rats were randomized into 3 groups,sham operation group (C group), resuscitation group (HS-R group) and propofol group (P group). There were 8 rats in each group. The animal model of hemorrhagic shock and resuscitation was established. Following resuscitation, the rats of HS-R group were infused normal saline at 1 mL·kg-1·h-1 with infusion pump for 2 hours, and rats of P group were infused propofol at 1 mL·kg-1·h-1 for 2 hours. The level of blood diamine oxidase (DAO) was measured in rats of groups. The intestinal tissue of 5 cm was taken. The levels of superoxide dismutase (SOD) and malondialdehyde (MDA) were measured using 3 cm of the tissue by xanthinoxidase method and thiobarbituric acid colorimetric technique. The other 2 cm of intestinal tissue was used to do HE staining to observe the changes of intestinal pathological histology. Results: The levels of MDA and DAO were higher in HS-R group and P group than those in C group (P 0.05),and were lower in P group than those of HS-R group(P 0.05). The level of SOD was lower in HS-R and P groups than that of C group (P 0.05), and it was higher in P group than that of HS-R group (P 0.05). The pathological grades of intestine were higher in P group and HS-R group than those in C group (P 0.05), but were lower in P group than those of HS-R group (P 0.05). Conclusion: The intestinal tissue was significantly damaged after hemorrhagic shock and resuscitation.Propofol can reduce this damage by against the oxygen free radicals in short-term.
出处 《天津医药》 CAS 北大核心 2011年第4期367-369,共3页 Tianjin Medical Journal
关键词 二异丙酚 休克 出血性 复苏术 小肠胺氧化酶(含铜) 超氧化物歧化酶 丙二醛 大鼠 Wistar propofol shock hemorrhagic resuscitation intestine small amine oxidase (copper-containing) superoxide dismutase malondialdehyde rats Wistar
  • 相关文献

参考文献9

二级参考文献30

  • 1祝小枫,熊德鑫,盛志勇.建立肠通透性改变测定方法[J].中国微生态学杂志,1994,6(4):36-38. 被引量:4
  • 2黎君友,于燕,郝军,晋桦,许惠君.分光光度法测定血和小肠组织二胺氧化酶活性[J].氨基酸和生物资源,1996,18(4):28-30. 被引量:202
  • 3Chen H, Xing B, Liu X, et al. Ozone oxidative preconditioning inhibits inflammation and apoptosis in a rat model of renal ischemia/reperfusion injury [ J ]. Eur J Pharmacol,2008, 581(3) :306-314.
  • 4Li Volti G, Sorrenti V, Murabito P, et al. Pharmacological induction of heme oxygenase - 1 inhibits iNOS and oxidative stress in renal ischemia - reperfusion injury [ J ]. Transplant Proc,2007, 39(10) :2986 - 2991.
  • 5Pallet MS, Hoidal JR, Ferris TF. Oxygen free radicals in ischemic acute renal failure in the rat [ J ]. Clin Invest, 1984,74(4) : 1156 - 1164.
  • 6Rah DK, Hart DW, Baek HS, et al. Protection of rabbit kidney from ischemia/reperfusion injury by green tea polyphenol pretreatment [ J ]. Arch Pharm Res, 2007, 30 ( 11 ) : 1447 - 1454.
  • 7Bojakowski K, Gaciong Z, Grochowiecki T, et al. Carbon monoxide may reduce ischemia reperfusion injury : a case report of complicated kidney transplantation from a carbon monoxide poisoned donor [ J ]. Transplant Proc, 2007,39 (9) :2928 - 2929.
  • 8Bayrak O, Turgut F, Karatas OF, et al. Oral beta - glucan protects kidney against ischemia reperfusion injury in rats [J]. Am J Nephrol,2008,28(2) :190 - 196.
  • 9Matsuyama M, Funao K, Kawahito Y, et al Study of cysteinyl leukotriene - 1 receptor in rat renal ischemia - reperfusion injury [ J ]. Transplant Proc, 2008,40 ( 7 ) : 2149 - 2151.
  • 10Jin YC, Kim W, Ha YM, et al. Propofol limits rat myocardial ischemia and reperfusion injury with an associated reduction in apoptotic cell death in vivo[ J ]. Vascul Pharmacol, 2009, 50 (1 -2) : 71 -77.

共引文献37

同被引文献63

引证文献5

二级引证文献20

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