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乙醇对灌注的正常、脂肪性和肝硬化大鼠肝脏代谢的影响。

Influence of ethanol on the metabolism of perfused normal, fatty and cirrhotic rat livers.

作者信息

Salaspuro M P, Mäenpää P H

出版信息

Biochem J. 1966 Sep;100(3):768-78. doi: 10.1042/bj1000768.

Abstract
  1. The influence of ethanol on the metabolism of perfused livers from normal rats and rats in various stages of development of dietary cirrhosis was studied. A choline-deficient, low-protein and high-fat diet was used. Results were obtained on oxygen consumption and carbon dioxide production, on glucose release and uptake by the liver and on changes in the concentrations of lactate and pyruvate and of beta-hydroxybutyrate and acetoacetate in the perfusion medium. 2. Oxygen consumption and carbon dioxide production were lower in fatty and cirrhotic livers than in normal livers. Ethanol had no effect on the oxygen consumption of any of the various livers. After addition of ethanol to the perfusion medium carbon dioxide production ceased almost completely in normal livers. Only a slight decrease in the carbon dioxide production occurred in fatty and cirrhotic livers. 3. With every type of liver glucose was released from the liver into the perfusion medium during the initial control period. This release continued after the addition of ethanol to the perfusion medium in experiments with normal and fatty livers, whereas with cirrhotic livers a marked uptake of glucose from the medium was found. A simultaneous release of the glycolytic end products lactate and pyruvate into the medium occurred. 4. The production of ketone bodies was equal in normal and early fatty livers (6 weeks on the fat diet). It was smaller in late fatty livers (3-4 months on the fatty diet) and in cirrhotic livers. 5. The lactate/pyruvate concentration ratio in the perfusion medium increased from 11 to 67 with normal livers, from 12 to 16 with early fatty livers, from 13 to 26 with late fatty livers and from 21 to 55 with cirrhotic livers when the livers were perfused with a medium containing ethanol. The beta-hydroxybutyrate/acetoacetate concentration ratio increased from 1.2 to 8.4 in normal livers, from 2.0 to 2.8 in early fatty livers, from 1.2 to 2.4 in late fatty livers and from 2.1 to 4.0 in cirrhotic livers when ethanol was added to the medium. 6. The effects of ethanol on liver metabolism during the development of dietary cirrhosis are discussed and related to human fatty liver and cirrhosis during chronic ethanol consumption.
摘要
  1. 研究了乙醇对正常大鼠以及处于饮食性肝硬化不同发展阶段大鼠的灌注肝脏代谢的影响。采用胆碱缺乏、低蛋白和高脂肪饮食。获得了关于氧气消耗和二氧化碳产生、肝脏对葡萄糖的释放和摄取以及灌注介质中乳酸和丙酮酸、β-羟基丁酸和乙酰乙酸浓度变化的结果。2. 脂肪肝和肝硬化肝脏的氧气消耗和二氧化碳产生低于正常肝脏。乙醇对任何一种肝脏的氧气消耗均无影响。向灌注介质中添加乙醇后,正常肝脏的二氧化碳产生几乎完全停止。脂肪肝和肝硬化肝脏的二氧化碳产生仅略有下降。3. 在初始对照期,每种类型的肝脏都有葡萄糖从肝脏释放到灌注介质中。在正常肝脏和脂肪肝的实验中,向灌注介质中添加乙醇后这种释放仍在继续,而在肝硬化肝脏中则发现有从介质中显著摄取葡萄糖的情况。同时有糖酵解终产物乳酸和丙酮酸释放到介质中。4. 正常肝脏和早期脂肪肝(高脂饮食6周)中酮体的产生量相等。晚期脂肪肝(高脂饮食3 - 4个月)和肝硬化肝脏中的酮体产生量较少。5. 当用含乙醇的介质灌注肝脏时,灌注介质中乳酸/丙酮酸浓度比在正常肝脏中从11增加到67,在早期脂肪肝中从12增加到16,在晚期脂肪肝中从13增加到26,在肝硬化肝脏中从21增加到55。当向介质中添加乙醇时,β-羟基丁酸/乙酰乙酸浓度比在正常肝脏中从1.2增加到8.4,在早期脂肪肝中从2.0增加到2.8,在晚期脂肪肝中从1.2增加到2.4,在肝硬化肝脏中从2.1增加到4.0。6. 讨论了乙醇在饮食性肝硬化发展过程中对肝脏代谢的影响,并将其与慢性乙醇摄入期间人类脂肪肝和肝硬化相关联。

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