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[在接受美他多辛药物治疗的背景下,酒精性肝病患者的抗阿司匹林试验动态]

[Dynamics of antipirin test at patients with alcoholic liver disease on the background of metadoksin drug receiving].

作者信息

Sil'vestrova S Iu, Fedotova S Iu, Drozdov T F, Petrakov A V

出版信息

Eksp Klin Gastroenterol. 2011(6):32-7.

Abstract

AIM

To study the effect of the drug metadoxin on drug-metabolizing liver function in patients with liver lesions alcoholic etiology (ALD).

MATERIALS AND METHODS

36 patients with ALD, of which 16 patients were diagnosed with hepatitis, while 20 - with the liver cirrhosis. All the patients underwent biochemical blood analysis and the study of drug-metabolizing liver function according to the pharmacokinetics of antipyrine in saliva before and after treatment with metadoxin. Metadoxin was administered at a dose of 500 mg once a day for 28 days. Concentrations of antipyrine in saliva samples were determined by HPLC. RESULTS. It was shown that of 36 patients examined in the 28-patients with ALD (group 2) there was a significant decrease in activity of liver enzymes according to the test with antipyrine (T1/2 = 28.7 +/- 3.4, CL = 17,9 +/- 5.2; p < 0,01 vs normal), whereas in 8 patients (group 1) was noted the typical for alcohol inductive influence on the activity of liver monooxygenases (T1/2 = 7.8 +/- 1.5, CL = 39.1 +/- 6.8; p < 0,05 vs normal). As a result of the 28-day therapy with metadoxin was a normalization of the pharmacokinetic parameters of AP in Gr. 1 (12.6 +/- 1.8; p < 0.05; NS vs normal) and a significant improvement of it in patients of Gr. 2 (17.9 +/- 5.2, vs N, p <0.05). Biochemical markers of ALD (AST/ALT, GGT, ALP) also demonstrated a positive dynamics in patients of both study groups. Correlation analysis of changes in CL and GGT (r1) and changes in AST/ALT and T1/2 (r2) showed a fairly high degree of correlation between these parameters (r1 = 0.58, r2 = 0.65).

CONCLUSION

The results showed marked improvement of drug-metabolizing liver function according to the test with antipyrine in patients with ALD after treatment with metadoxin.

摘要

目的

研究美他多辛对酒精性病因所致肝脏病变(ALD)患者肝脏药物代谢功能的影响。

材料与方法

36例ALD患者,其中16例诊断为肝炎,20例诊断为肝硬化。所有患者在美他多辛治疗前后均接受了血液生化分析,并根据唾液中安替比林的药代动力学研究了肝脏药物代谢功能。美他多辛的给药剂量为500mg,每日1次,共28天。通过高效液相色谱法测定唾液样本中安替比林的浓度。结果:在36例接受检查的患者中,28例ALD患者(第2组)经安替比林试验显示肝酶活性显著降低(T1/2 = 28.7 +/- 3.4,CL = 17.9 +/- 5.2;与正常组相比,p < 0.01),而8例患者(第1组)表现出酒精对肝脏单加氧酶活性的典型诱导影响(T1/2 = 7.8 +/- 1.5,CL = 39.1 +/- 6.8;与正常组相比,p < 0.05)。经过28天的美他多辛治疗,第1组患者安替比林的药代动力学参数恢复正常(12.6 +/- 1.8;p < 0.05;与正常组相比无显著性差异),第2组患者的药代动力学参数显著改善(17.9 +/- 5.2,与正常组相比,p < 0.05)。两个研究组患者的ALD生化指标(AST/ALT、GGT、ALP)也均呈现出积极的变化趋势。CL与GGT变化之间的相关性分析(r1)以及AST/ALT与T1/2变化之间的相关性分析(r2)显示,这些参数之间具有较高的相关性(r1 = 0.58,r2 = 0.65)。

结论

结果显示,美他多辛治疗后,ALD患者经安替比林试验测得的肝脏药物代谢功能有显著改善。

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