首页> 外文期刊>European journal of clinical investigation >Ursodeoxycholic acid reduces lipid peroxidation and mucin secretagogue activity in gallbladder bile of patients with cholesterol gallstones.
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Ursodeoxycholic acid reduces lipid peroxidation and mucin secretagogue activity in gallbladder bile of patients with cholesterol gallstones.

机译:熊去氧胆酸降低胆固醇胆结石患者胆囊胆汁中脂质过氧化和粘蛋白促分泌活性。

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BACKGROUND: Recently it has been postulated that gallbladder mucin hypersecretion observed in the pathogenesis of cholesterol gallstone disease may be induced by biliary lipid peroxidation. Ursodeoxycholic acid treatment reduces mucin concentration and the formation of cholesterol crystals in the gallbladder bile of patients with cholesterol gallstones and this effect might be mediated by a decrease of biliary lipid peroxidation. MATERIAL AND METHODS: In a double-blind, placebo-controlled trial patients with symptomatic cholesterol gallstones received either ursodeoxycholic acid (750 mg daily) (n = 10) or placebo (n = 12) 10-12 days prior to cholecystectomy. As a marker for lipid peroxidation malondialdehyde was measured in bile together with mucin concentration. In addition, the mucin secretagogue activity of the individual bile samples was assessed in cultured dog gallbladder epithelial cells. RESULTS: Ursodeoxycholic acid therapy resulted in a significant reduction of lipid peroxidation in bile as determined by the biliary malondialdehyde concentration (1.36 +/- 0.28 vs. 2.05 +/- 0.38 micromol L(-1); P < 0.005) and the malondialdehyde (micromol L(-1))/total bile acid (mmol L(-1)) ratio (0.02 +/- 0.005 vs. 0.06 +/- 0.01; P < 0.001). Furthermore, a decrease in mucin concentrations (0.7 +/- 0.3 vs. 1.3 +/- 0.5 mg mL(-1); P < 0.005) and of the mucin secretagogue activity of gallbladder bile (0.9 +/- 0.2 vs. 2.2 +/- 0.3 times control; P < 0.001) was observed. CONCLUSIONS: The reduction of lipid peroxidation and mucin secretagogue activity of gallbladder bile induced by ursodeoxycholic acid treatment may contribute to the beneficial effects of this drug on gallbladder bile composition and symptoms in cholesterol gallstone patients.
机译:背景:最近,有人推测胆汁脂质过氧化作用可能是胆固醇胆结石病发病机理中观察到的胆囊粘蛋白分泌过多。熊去氧胆酸治疗可降低胆囊胆固醇结石患者胆囊黏液中的粘蛋白浓度和胆固醇晶体的形成,这种作用可能是由胆汁脂质过氧化作用的降低所介导的。材料与方法:在一项有症状胆固醇胆结石的双盲,安慰剂对照试验中,胆囊切除术前10-12天接受熊去氧胆酸(每天750 mg)(n = 10)或安慰剂(n = 12)。作为脂质过氧化的标志物,在胆汁中测量丙二醛与粘蛋白浓度。另外,在培养的狗胆囊上皮细胞中评估了单个胆汁样品的粘蛋白促分泌活性。结果:熊去氧胆酸治疗导致胆汁中脂质过氧化的显着降低,这取决于胆汁丙二醛浓度(1.36 +/- 0.28 vs. 2.05 +/- 0.38 micromol L(-1); P <0.005)和丙二醛(微摩尔L(-1))/总胆汁酸(mmol L(-1))的比率(0.02 +/- 0.005对0.06 +/- 0.01; P <0.001)。此外,粘蛋白浓度降低(0.7 +/- 0.3 vs. 1.3 +/- 0.5 mg mL(-1); P <0.005)和胆囊胆汁的粘蛋白促分泌活性降低(0.9 +/- 0.2 vs. 2.2 + +/- 0.3倍对照; P <0.001)。结论:由熊去氧胆酸治疗引起的胆囊胆汁脂质过氧化和粘蛋白促分泌活性的降低可能有助于该药物对胆固醇胆结石患者胆囊胆汁成分和症状的有益作用。

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