酒精对肝脏代谢的影响

Kanzo Pub Date : 1974-01-25 DOI:10.2957/KANZO.15.1
K. J. Isselbacher
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引用次数: 7

摘要

尽管关于酒精代谢的途径一直存在相当大的争议,但仍然可以肯定地说,负责乙醇氧化的主要酶是酒精脱氢酶。这种酶存在于肝细胞的细胞质中。酒精氧化还有另外两种机制:1)过氧化氢酶和过氧化氢过氧化;2)微粒体乙醇氧化。包括我们自己的实验室在内的许多实验室都试图确定微粒体乙醇氧化的机制,以及该系统在酒精的整体代谢中是否具有任何生理或临床意义。我们获得的大多数证据表明,微粒体乙醇氧化可以在体外证明是两种酶反应的净结果:1)NADPH氧化酶和2)过氧化氢酶。这两种酶的相互作用导致过氧化氢的产生,过氧化氢反过来又将乙醇氧化为乙醛。证据这一概念的解释微粒体乙醇氧化将提出。酒精的影响之一是造成脂肪肝。产生脂肪肝的原因有:1)脂肪酸合成增加,2)脂肪酸氧化减少,3)脂肪酸酯化增加,4)脂蛋白载脂蛋白形成减少,5)脂肪酸向肝脏的动员增加,6)脂蛋白从肝脏释放减少。酒精会影响许多这些过程。然而,许多现有证据表明,脂肪酸氧化减少可能是导致酒精引起脂肪肝的最重要因素。一般来说,肝脏中的脂肪以甘油三酯的形式存在,以两种类型的颗粒存在,一种是30-80A的小颗粒,另一种是>200A的颗粒。较小的颗粒代表正在准备出口的脂蛋白。较大的颗粒代表在肝脏中积聚的脂质。酒精对肝脏的影响之一是产生高脂血症。这似乎是由于肝脏脂蛋白合成增加,最常见于甘油三酯水平升高的个体,特别是那些具有IV型高脂蛋白血症潜在缺陷的个体。低血糖与酒精一起发生,但只有当肝脏的糖原储存因营养不良或禁食而耗尽时才会发生。我们将讨论肝脏的其他代谢作用。最后,除了对肝脏的影响,我们还了解到酒精对肠道的重要作用。这包括:(1)肠道脂质合成增加,导致脂肪肝;(2)维生素B12吸收减少;(3)糖和氨基酸运输减少;(4)钙吸收减少。酒精对肠道的这些影响可能导致酒精受试者的营养受损。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Metabolic Effects of Alcohol on the Liver
Although there has been considerable debate as to the pathways of alcohol metabolism, It still can be stated with confidence that the main enzyme responsible for ethanol oxidation is alcohol dehydrogenase. This enzyme is found in the cytoplasm of the liver cell. There are two other mechanisms for the oxidation of alcohol: 1) catalase and catalatic peroxidation; and 2) microsomal ethanol oxidation. Many laboratories including our own have attempted to determine the mechanism of microsomal ethanol oxidation and whether this system has any physiologic or clinical significance in the overall metabolism of alcohol. Most of the evidence that we have obtained would suggest that microsomal ethanol oxidation which can be demonstrated in vitro is the net result of two enzyme reactions: 1) NADPH oxidase and 2) catalase. The interactions of these two enzymes lead to the production of hydrogen peroxide which in turn serves to oxidize ethanol to acetaldehyde. Evidence for this concept as an explanation of microsomal ethanol oxidation will be presented.One of the effects of alcohol is the production of a fatty liver. Fatty liver can be produced by: 1) increased fatty acid synthesis, 2) decreased fatty acid oxidation, 3) increased fatty acid esterification, 4) decreased formation of the apoproteins of lipoproteins, 5) increased mobilization of fatty acids to the liver and 6) decreased release of lipoproteins from the liver. Alcohol affects many of these processes. Much of the available evidence indicates, however, that decreased fatty acid oxidation is probably the most significant factor in leading to the production of the fatty liver produced by alcohol. In general the fat in the liver is present in the form of triglyceride and is present in two types of particles, a small 30-80A particle and the other>200A. The smaller particle represents the lipoproteins which are being prepared for export. The larger particles represent the lipid being accumulated in the liver.One of the features of alcohol on the liver is the production of hyperlipemia. This appears to be due to increased synthesis of lipoproteins by the liver and is most common in individuals who already have an elevated triglyceride level especially those with an underlying defect in type IV hyperlipoproteinemia.Hypoglycemia occurs with alcohol but only when the glycogen stores of the liver have been depleted due to poor nutrition or fasting. The other metabolic effects of the liver will be discussed.Finally in addition to the effects on the liver we have come to learn of important actions of alcohol on the intestine. These include: 1) increase in lipid synthesis by the intestine which contributes to the fatty liver, 2) decreased vitamin B12 absorption, 3) decreased sugar and amino acid transport and 4) decrease in calcium absorption. These effects of alcohol on the intestine may contribute to the impaired nutrition seen in alcoholic subjects.
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