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大黄素抗大鼠肝移植急性排斥反应的实验研究
  • 期刊名称:中华中医药杂志
  • 时间:0
  • 分类:R657.3[医药卫生—临床医学;医药卫生—外科学] R-332
  • 作者机构:[1]温州医学院附属第二医院,温州325027
  • 相关基金:国家自然科学基金资助项目(No.30572395)
  • 相关项目:大黄素对大鼠原位肝移植排斥反应的作用及其机制研究
中文摘要:

目的:探讨大黄素对大鼠肝移植术后急性排斥反应的抑制作用。方法:建立LEW→BN大鼠肝移植动物模型,随机分为A组(排斥反应组)、B组(CsA组)、C组(大黄素组)3组,每组15只大鼠,术后每天分别腹腔注射生理盐水0.5ml/d、环孢素A(CsA)10.0mg·kg^-1·d^-1、大黄素50.0mg·kg^-1·d^-1,连续用药8天,停药后每组处死6只大鼠取肝脏组织观察急性排斥活动指数(RAI)和肝细胞凋亡指数(AI),其余大鼠继续饲养以观察存活期。结果:A、B、C组大鼠存活期(天)分别为9.50±1.64、21.57±2.15、21.29±2.21,B、C组存活期较A组明显延长(/9〈0.01),B、C组间存活期无明显差别(P〉0.05)。A、B、C组RAI分别是7.67±0.98、5.17±0.40、5.83±0.75,A1分别是35.83±2.32、15.83±1.33、16.50±2.35。B、C组的RAI、AI较A组均明显降低(P〈0.01),B、C组间差别均无意义(P〉0.05)。结论:大黄素能有效减少大鼠肝移植术后肝细胞的凋亡,抑制肝移植术后急性排斥反应。

英文摘要:

Objective: To evaluate the effect of emodin on acute rejection after orthotopic liver transplantation (OLT) in rats. Methods : The LEW→BN OLT models were established. A total of 45 rats were divided randomly and equally into 3 groups: group A was treated with normal saline at dose of 0.5 ml/d intraperitoneally from 1st day to 8th day after operation; Group B, CsA at dose of 10.0 mg·kg^-1·d^-1 ; Group C, emodin at dose of 50.0 mg·kg^-1·d^-1. 8 days after operation, 6 recipients of each groups were killed for confirming rejection-active index (RAI) and hepatocellular apoptosis index (AI) by observing the pathologic change of transplanted liver in recipients. The other recipients were raised for observing the survival time. Results: Respectively, the survival time(days) of group A,B,C was 9.50±1.64,21.57±2.15,21.29±2.21. The survival time of group B,C was significantly longer than that of group A ( P〈0.01 ) and there was no significant distinction between group B and C in survival time (P〉0.05). Respectively, the RAI of group A ,B,C was 7.67±0.9,5.17±0.40,5.83±0.75 and the AI of group A,B,C was 35.83±2.32,15.83±1.33,16.50±2.35. The RAI and AI of group B,C was significantly lower than that of group A ( P〈0.01 ) and there was no significant distinction between group B and C in RAI and AI ( P〉0.05 ) . Conclusion : Emodin can reduce the hepatocellular apoptosis and suppress the acute rejection after OLT in rats.

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