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血小板激活因子拮抗剂BN52021对缺血再灌注损伤的大鼠肝脏的保护作用 被引量:2

Protection of BN 52021 on Liver IschemiaReperfusion Injuries in Rats
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摘要 目的:研究血小板激活因子拮抗剂BN52021对大鼠缺血再灌注肝脏的影响。方法:将大鼠分为三组,对照组未进行缺血及药物治疗;缺血再灌注组行40min缺血,然后行120min再灌注;血小板激活因子拮抗剂治疗组行40min缺血,120min再灌注,再灌注时给予BN52021(10mg/kg),比较各组血清SGPT、SGOT、AKP及γ-GT,肝脏的细胞能荷。结果:用血小板激活因子拮抗剂治疗组血清SGPT、SGOT、AKP、γGT均较缺血再灌注组显著降低,能荷水平明显升高。结论:血小板激活因子拮抗剂BN52021用于大鼠肝脏缺血再灌注可减少肝脏的损害,提示血小板激活因子(PAF)对肝脏缺血再灌注损伤的发生起一定的作用,血小板激活因子拮抗剂BN52021有可能用于肝脏缺血再灌注损伤的治疗。 Objective: Plateletactivating factor antagonist BN 52021 on ischemia-reperfusion(I/R)injury of rat liver was studied.Methods: Rats were divided into 3 groups.The normal control group was not subjected to hepatic ischemia and no treatment was given.The I/R injury group was subjected to 40 minutes of ischemia followed by reperfusion for 120 minutes.The AntiPAF treatment group was subjected of reperfusion and BN 52021 10 mg/kg was administered at reperfusion SGPT,SGOT,AKP and γGT and hepatic energy charge were compared.Results: The antiPAF treatment group serum levels of SGPT,SGOT,AKP and γGT were significantly lower than I/R injury group. Energy charge level was significantly higher with antiPAF treatment (P<0.05).Conclusion: AntiPAF BN 52021 treatment at reperfusion decreased damage of rat liver subjected to I/R injury.AntiPAF BN 52021 may be useful in the treatment of hepatic I/R injury.
出处 《河南医学研究》 CAS 1998年第1期10-13,共4页 Henan Medical Research
关键词 肝脏 缺血再灌注 血小板激活因子 BN52021 liver ischemiareperfusion PAF BN 52021
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  • 1张毅,叶启发,明英姿,许贤林,肖建生,李远明.三七总皂甙预处理大鼠供肝对细胞凋亡及TNF-α、Caspase-3 表达的影响a(英文)[J].中国现代医学杂志,2005,15(2):172-176. 被引量:9
  • 2肖建生,叶启发,蔡方刚,牛英,张毅,许贤林.缺血预处理对大鼠肝缺血再灌注后即早基因c-fos、c-jun表达的影响[J].中国现代医学杂志,2005,15(6):843-846. 被引量:3
  • 3夏仁品,武聚山,吴娟,卢实春,郭庆良,黄建文,赵春惠,Terry B Strom.大鼠原位肝移植后肿瘤坏死因子-α与供肝损伤的关系[J].首都医科大学学报,2005,26(4):489-491. 被引量:3
  • 4刘艳秋,游松,田代真一,小野寺敏,池岛乔.冬凌草甲素通过激活ERK途径诱导U937细胞凋亡[J].中国中药杂志,2005,30(23):1856-1859. 被引量:11
  • 5Chandmssekaran K, Mehrabian Z, Spinmewyn B, et al. Neuroprotective effects of bilobalide, a component of the Ginkgo biloba extract (EGb 761), in gerbil global brain ischemia[J]. Brain Res,2001,922(2) :282-292.
  • 6Maitra 1, Marcocci L, Droy-lefaix MT, et al. Peroxyl radicals cavenging activity of Ginkgo biloba extract Egb 761 [ J ]. Biochem Pharmacol, 1995,49(11): 1649-1655.
  • 7Baranes J, Hellegouarch A, Le Hegarat M, et al. The effects of PAF-acether on the cardiovascular system and their inhibition by a new highly specific PAF-acether reeceptor antagonists BN 52021 [J]. Pharmacol Res Commun, 1986,18(8) :717-737.
  • 8Tosaki, Engelman DT, Pali T, et al. Ginkgo biloba extract (EGb 761) improves postischemic function in isolated preconditioned working rat hearts[J]. Coron Artery Dis, 1994,5(5) :443-450.
  • 9Varga E, Bodi A, Ferdinandy P, et al. The protective effect of EGb 761 in isolated ischemic/reperfused rat hearts: a link between cardiac function and nitric oxide production [J ]. J Cardiovasc Pharmacol,1999,34(5) :711-717.
  • 10Liebgott T, Miollan M, Berchadsky Y, et al. Complementary cardioprotective effects of flavonoid metabolites and terpenoid constituents of Ginkgo biloba extract (EGb 761) during ischemia and repearfusion[J].Basic Res Cardiol,2000,95(5) :368-377.

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