期刊文献+

多烯磷脂酰胆碱注射液治疗肝功能损害的疗效观察 被引量:2

下载PDF
导出
摘要 目的观察多烯磷脂酰胆碱注射液治疗各种病因引起的肝损害疗效。方法选择各种原因引起的肝功能损害患者119例,随机分为治疗组和对照组。治疗组:给予多烯磷脂酰胆碱注射液465 mg静滴,每日1次。对照组:给予葡醛酸钠注射液0.532 g,每日1次,疗程均为14 d。观察两组治疗前后肝功能及预后情况。结果治疗14 d后,治疗组患者症状体征改善情况优于对照组,治疗组显效及有效51例(85.0%),对照组显效及有效34例(57.6%),治疗组肝功能损害恢复情况优于对照组,两组差异显著(P<0.05)。结论多烯磷脂酰胆碱明显改善肝功能损害和临床症状,疗效显著。 Objective To observe the curative effect of Polyene Phosphatidylcholine injection on liver injury caused by different diseases. Methods 119 patients who suffered from liver injury were randomly divided into two groups: treatment group and control group. Treatment group: injected Polyene phosphatidylcholine injection 465 mg, once a day. Control group: injected sodium glucuronic Acid Injection 0.532 g, once a day; course of treatment was 14 days in two groups. The curative effect on liver function and prognosis of the two groups before and after treatment were observed. Results After 14-day treatment, patients' symptoms of the treatment group improved more obviously than those of the control group, and 51 cases achieved excellent effects (85.0%) in the treatment group, while 34 cases achieved excellent effects (57.6%). The treatment group was superior to the control group in reviving Liver Injury. There were significant difference among different groups(P〈0.05). Conclusion Polyene phosphatidylcholine injection could obviously improve liver injury and clinical symptoms, the curative effect is remarkable.
出处 《当代医学》 2013年第29期135-136,共2页 Contemporary Medicine
关键词 肝损害 葡醛酸钠注射液 多烯磷脂酰胆碱注射液 Liver injury Sodium glucuronic acid injection Polyene phosphatidylcholine injection
  • 相关文献

参考文献8

  • 1Report of an international consensus meeting.Benichou C.Criteria of drug-induced liver disorders[J]. J hepatol, 1990,11 (2): 272-276.
  • 2刘梅,陆伦根,曾民德.多烯磷脂酰胆碱对肝细胞保护机制的研究进展[J].肝脏,2006,11(1):43-45. 被引量:98
  • 3Xu YQ.Lieber 0$ DLPO attenuated alcohol-induced cytotoxicity in HepG 2 cells expressing CYP 2 E I [J]. Alcohol Alcohol, 2005,40: ]. 72-175.
  • 4A].eynik MK,Leo MA,Aleynik 8l,et al.Polyenylphosphat idyl choline opposes the increase of cytochrome P-4502E]. by ethanol and corrects it's iron-induced decrease[J]. Alcohol Ciin Exp &es, 1999,25:96-100.
  • 5Lieber C8.Alcoholic fatty liver:its pathogenesis and mechanism of progression to inflammation and fibrosis[J]. Alcohol, 2004,34: 9-I 9.
  • 6Lieber C$.Pathogenesis and treatment of alcoholic liver disease: progress over the last 50 years[J].Eocz Akad Med Bialymst,2005,50: 7-20.
  • 7包晗,陈源.多烯磷脂酰胆碱与维生素E联合治疗肝功能异常脂肪肝疗效观察[J].山西医药杂志(下半月),2010,39(5):445-446. 被引量:1
  • 8郭开生.熊去氧胆酸治疗脂肪肝的疗效[J].中华综合医学,2001,2(2):103-104. 被引量:6

二级参考文献23

  • 1Adachi M,Ishii H.Role of mitochondria in alcoholic liver injury.Free Radic Biol Med,2002,32:487-491.
  • 2Mak KM,Wen KF,Ren CL,et al.Dilinoleoylphosphatidylcholine reproduces the antiapoptotic actions of polyenylphosphatidylcholine against ethanol-induced hepatocyte apoptosis.Alcohol Clin Exp Res,2003,27:997-1005.
  • 3Navder KP,Lieber CS.Dilinoleoylphosphatidylcholine is responsible for the beneficial effects of polyenylphosphatidylcholine on ethanol-induced mitochondrial injury in rats.Biochem Biophys Res Commun,2002,291:1109-1112.
  • 4Katz GG,Shear NH,Malkiewicz IM,et al.Signaling for ethanol-induced apoptosis and repair in vitro.Clin Biochem,2001,34:219-227.
  • 5Cao Q,Mak KM,Lieber CS.Dilinoleoylphosphatidylcholine prevents transforming growth factor-β1-mediated collagen accumulation in cultured rat hepatic stellate cells.J Lab Clin Med,2002,139:202-210.
  • 6Cao Q,Mak KM,Lieber CS.DLPC decreases TGFβ1-induced collagen mRNA by inhibiting p38 MAPK in hepatic stellate cells.Am J Physiol Gastrointest Liver Physiol,2002,283:G1051-G1061.
  • 7Lieber CS.Pathogenesis and treatment of alcoholic liver disease:progress over the last 50 years.Rocz Akad Med Bialymst,2005,50:7-20.
  • 8Lieber CS.Alcoholic fatty liver:its pathogenesis and mechanism of progression to inflammation and fibrosis.Alcohol,2004,34:9-19.
  • 9Tanaka H,Miyano M,Ueda H,et al.Changes in serum and red blood cell membrane lipids in patients treated with interferon ribavirin for chronic hepatitis C.Clin Exp Med,2005,5:190-195.
  • 10Bai J,Cederbaum AI.Overexpression of CYP2E1 in mitochondria sensitizes HepG2 cells to the toxicity caused by depletion of glutathione.J Biol Chem,2005,27:1-24.

共引文献101

同被引文献24

引证文献2

二级引证文献3

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