胆管结扎术后胆汁性肝硬化发生过程中肝脏和血浆中谷胱甘肽的状态。

E Purucker, R Winograd, E Roeb, S Matern
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引用次数: 31

摘要

在肝硬化的发展过程中,还原性谷胱甘肽(GSH)和氧化性谷胱甘肽(GSSG)发生的变化我们所知不多。因此,我们研究了大鼠胆管结扎术后肝硬化发展过程中的谷胱甘肽氧化还原系统。我们比较了胆管结扎大鼠和假手术对照组术后6、24 h和5、15、23、38 d肝脏和血浆中GSH和GSSG含量。与对照组相比(x +/- SD: 6.07 +/- 0.52 μ mol/g wet wt.),胆管结扎后24小时(+ 37%)和5天(+ 53%)肝脏GSH显著升高。此后,GSH持续下降至4.25 +/- 0.64 μ mol/g (-31%;P < 0.001)。胆管结扎5天后,高GSH浓度大鼠的GSH周转量与假手术对照组(胆管结扎后16 nmol/min / g,对照组15 nmol/min / g)无显著差异。GSSG(对照组211 +/- 42 nmol/g wet wt.)在胆管结扎后6和24 h显著降低(分别为-34%和-43%)。此后,GSSG增加,在23天和38天后,GSSG比对照组高约100%。胆管结扎后肝脏GSSG与GSH的关系由3.4持续升高至20.5%。血浆GSH (9.57 +/- 0.79 μ mol/l)的变化过程与肝脏GSH的变化过程相似,在较低水平上:第5天+ 14%,第15天-41%,观察期结束时-51%。血浆GSSG (0.99 +/- 0.31 μ mol/l)与肝脏GSSG呈负相关:胆管结扎后早期浓度升高(第5天:+ 91%),观察期末浓度降低(-44%)。胆管结扎术后肝硬化发生过程中谷胱甘肽状态发生动态变化。这些变化与肝脏氧化应激增加和GSSG从细胞转运到血浆的缺陷是一致的。
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Glutathione status in liver and plasma during development of biliary cirrhosis after bile duct ligation.

We do not know much about the changes that occur in reduced (GSH) and oxidized (GSSG) glutathione in the development of liver cirrhosis. Therefore, we investigated the glutathione redox system during development of liver cirrhosis after bile-duct ligation in rats. We compared the GSH and GSSG content of liver and plasma between bile-duct-ligated rats and sham-operated controls 6 and 24 h and 5, 15, 23, and 38 days after operation. Compared to controls (x +/- SD: 6.07 +/- 0.52 mumol/g wet wt.), liver GSH significantly increased 24 h (+ 37%) and 5 days (+ 53%) after bile-duct ligation. Thereafter, GSH continuously declined to 4.25 +/- 0.64 mumol/g (-31%; P < 0.001) at the end of the observation period after 38 days. The GSH turnover in 5-day bile-duct-ligated rats with high GSH concentrations was not significantly different than in sham-operated controls (16 nmol/min per g after bile-duct ligation and 15 nmol/min per g in controls). GSSG (211 +/- 42 nmol/g wet wt. in controls) was significantly lower 6 and 24 h after bile-duct ligation (-34% and -43%, respectively). Thereafter, GSSG increased and was about 100% higher than in controls after 23 and 38 days. The relation of GSSG to GSH in liver continuously increased from 3.4 to 20.5% after bile-duct ligation. The course of plasma GSH (9.57 +/- 0.79 mumol/l) paralleled hepatic GSH on a lower level: + 14% at day 5, -41% at day 15 and -51% at the end of the observation period. Plasma GSSG (0.99 +/- 0.31 mumol/l) was inversely related to liver GSSG: there were increased concentrations early after bile duct ligation (day 5: + 91%) and reduced concentrations (-44%) at the end of the observation period. Dynamic changes of the glutathione status occur in the development of liver cirrhosis after bile-duct ligation. These changes are consistent with increased oxidative stress in the liver and a deficit of transporting GSSG from the cells into plasma.

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