期刊文献+

双环醇治疗肾移植术后肝损伤的应用 被引量:1

Application of bicyclol in patients with hepatic lesion after kidney transplantation
下载PDF
导出
摘要 目的:研究双环醇治疗肾移植术后环孢素致肝损伤的疗效。方法:12例因环孢素致肝损伤的肾移植术后患者每日口服双环醇75mg,持续给药2周。口服双环醇前后患者自肘静脉采血,在自动生化分析仪上测定肝功能,并以特异性荧光偏振免疫法测定环孢素全血药物浓度。结果:全部12例肾移植术后患者在口服双环醇(75mg)2周后,血清丙氨酸氨基转移酶(ALT)、天冬氨酸氨基转移酶(AST)均显著下降(P<0.01),ALT水平从(126.8±99.3)U/L显著降至(31.5±12.4)U/L(P<0.01),AST水平从(67.4±55.5)U/L显著降至(29.6±14.9)U/L;同时环孢素血药浓度明显降低(P<0.05),从(243.72±67.22)ng/mL减少至(157.71±54.73)ng/mL。12例患者中没有观察到药物不良反应。结论:双环醇能有效且比较安全地应用于肾移植术后环孢素致肝损伤患者,但环孢素血药浓度有改变,应注意临床监测。 Objective:The efficacy of bicyclol in patients with hepatic lesion induced by cyclosporine after kidney transplantation was investigated.Methods: 12 renal transplanted recipients with eyclnsporine induced hepatic lesion were given bicyelol 75mg per day for 2 weeks. Before and after the bicyclol treatment,venous blood was collected from antecubital vein.Hepatic function was determined on a biochem auto-an-alyzer and eyclosporine whole blood concentrations were measured by a fluorescence polarization immunoassay.Results: After the bicyelol treatment of 2 weeks,ALT and AST levels were decreased significantly (P<0.01),with ALT from(126.8±99.3)U/L to(31.5±12.4)U/L and AST from (67.4±55.5)U/L to (29.6±14.9) U/L,respectively. While the cyclosporine whole blood concentrations were decreased too(P<0.05),from(243.72±67.22)ng/mL to (157.71±54.73)ng/mL.No severe adverse drug reaction was observed in 12 renal transplanted recipients.Conclusions:The results indicated that bicyclol would be applied to with hepatic lesion induced by cyclosporine after renal transplantation effectively and safely. Therapeutic drug monitoring should be paid attention on the patients due to the change of cyclospofine level.
作者 周甘平 徐峰
出处 《中国药物应用与监测》 CAS 2004年第4期7-8,共2页 Chinese Journal of Drug Application and Monitoring
关键词 双环醇 环孢素 肝毒性 肾移植 Bicyclol Cyclosporine Hepatic lesion Renal transplantation
  • 相关文献

二级参考文献15

  • 1[1]Geoffrion Y, Rydzy M. The use of immobilized ferrite to enhance the depth selectivity of in vivo surface coil NMR spectroscopy [J] . NMR Biomed, 1988,1(3) :107 - 112.
  • 2[2]Jehenson P. Correction for the contamination by muscle signal of in vivo 31P-NMR spectra of the liver and kidney [J] . J Magn Resonance, 1992,96:181 - 184.
  • 3[3]Malloy CR, Cunningham CC, Radda GK, et al. The metabolic state of the rat liver in vivo measured by31 P-NMR spectroscopy [J]. Biochim Biophys Acta, 1986,885:1 - 11.
  • 4[4]Berson A, Renault S, Letteron P, et al. Uncoupling of rat and human mitochondria: a possible explanation for tacrineinduced liver dysfunction [J]. Gastroenterlogy, 1996,110:1878 - 1890.
  • 5[5]Watanabe H, Kobayashi A, Yamamoto T, et al. Alterations of human erythrocyte membrane fluidity by oxygen-derived free radicals and calcium [J]. Fre Rad Biol Med, 1990,8:507 - 511.
  • 6[6]Parmar DV, Ahmed G, Khandkar MA, et al. Mitochondrial ATPase: a target for paracetamol-induced hepatotoxicity [J].Eur J Pharmacol, 1995,293: 225 - 229.
  • 7[7]Takahashi H, Geoffrion Y, Butler K, et al. In vivo hepatic energy metabolism during the progression of alcoholic liver diseases: a noninvasive 31P NMR study in rats [J]. Hepatology, 1990,11(1) :65 - 73.
  • 8[8]Meyers LL, Beierschmitt WP, Khairallah EA, et al. Acetaminophen-induced inhibition of hepatic mitochondrial respiration in mice [J]. Toxicol App Pharamcol, 1988,93:378 - 388.
  • 9[9]Katyare SS, Satav JG. Impaired mitoehondrial oxidative energy metabolism following paracetamol-induced hepatotoxicity in the rat [J]. Br J Pharmacol, 1989,96:51- 58.
  • 10Guo Qing Zang Xia Qiu Zhou Hong Yu Qing Xie Guo Ming Zhao Bin Wang Qing Guo Yue Qin Xiang Dan Liao Department of Infectious Diseases,Rujin Hospital,Shanghai Second Medical University,Shanghai 200025,China.Effect of hepatocyte apoptosis induced by TNF-α on acute severe hepatitis in mouse models[J].World Journal of Gastroenterology,2000,6(5):688-692. 被引量:30

共引文献88

同被引文献6

引证文献1

二级引证文献33

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