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Reduced hepatic glycogen stores in patients with liver cirrhosis.

机译:肝硬化患者肝糖原存储减少。

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BACKGROUND: Patients with alcoholic liver cirrhosis have reduced hepatic glycogen stores but the mechanisms leading to this finding are not clear. METHODS: We therefore determined the hepatic glycogen content in patients with alcoholic (n = 9) or biliary cirrhosis (n = 8), and in control patients undergoing liver surgery (n = 14). All patients were in the postabsorptive state. In addition, we performed a morphometric analysis of the livers, and measured activities and mRNA expression of several enzymes involved in glycogen metabolism. Cirrhotic and control patients were similar regarding age and body weight. RESULTS: Cirrhotic patients had a reduced glycogen content per gram liver wet weight (17 +/- 11 versus 45 +/- 17 mg/g, P < 0.05), per milliliter hepatocytes (28 +/- 16 versus 52 +/- 21 mg/ml, P < 0.05) and per liver (28 +/- 17 versus 64 +/- 22 g, P < 0.05), the reduction being observed in both patients with alcoholic or biliary cirrhosis. Liver histology confirmed these findings and revealed that the decrease in liver glycogen in cirrhotic patients was not homogeneous across cirrhotic lobules. Activities of glycogen synthase and phosphorylase (total activity and active form) were not different between cirrhotic and control patients, whereas hepatic mRNA expression was decreased in cirrhotics by approximately 50%. The activity of glucokinase was decreased in cirrhotic as compared in control patients (0.06 +/- 0.30 versus 0.42 +/- 0.21 U/ml hepatocytes, P < 0.05), the reduction being observed in both patients with alcoholic or biliary cirrhosis. CONCLUSIONS: We conclude that patients with alcoholic or biliary cirrhosis have decreased hepatic glycogen stores per volume of hepatocytes and per liver. Decreased activity of glucokinase may represent an important mechanism leading to this finding.
机译:背景:酒精性肝硬化的患者肝糖原储备减少,但导致这一发现的机制尚不清楚。方法:因此,我们确定了酒精中毒(n = 9)或胆汁性肝硬化(n = 8)患者和进行肝手术的对照患者(n = 14)的肝糖原含量。所有患者均处于吸收后状态。此外,我们对肝脏进行了形态分析,并测量了参与糖原代谢的几种酶的活性和mRNA表达。肝硬化和对照患者的年龄和体重相似。结果:肝硬化患者每毫升肝细胞中每克肝湿重糖原含量降低(17 +/- 11对45 +/- 17 mg / g,P <0.05)(28 +/- 16对52 +/- 21) mg / ml,P <0.05)和每肝(28 +/- 17 vs 64 +/- 22 g,P <0.05),在酒精性或胆汁性肝硬化患者中均观察到减少。肝组织学证实了这些发现,并揭示了肝硬化患者肝小叶之间肝糖原的减少不均匀。肝硬化患者和对照组患者的糖原合酶和磷酸化酶活性(总活性和活性形式)没有差异,而肝硬化患者肝mRNA表达降低约50%。与对照组相比,肝硬化患者的葡萄糖激酶活性降低(0.06 +/- 0.30对0.42 +/- 0.21 U / ml肝细胞,P <0.05),在酒精性或胆汁性肝硬化患者中均观察到降低。结论:我们得出结论,酒精性或胆汁性肝硬化患者每单位肝细胞和每肝脏的肝糖原储备减少。葡萄糖激酶活性降低可能是导致该发现的重要机制。

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