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乙醇对酮体代谢的影响。

Effect of ethanol on ketone metabolism.

作者信息

Lefèvre A, Adler H, Lieber C S

出版信息

J Clin Invest. 1970 Oct;49(10):1775-82. doi: 10.1172/JCI106395.

Abstract

Ketonuria has been observed in alcoholics. To study the mechanism of this effect, healthy, volunteers were given adequate diets (36% of calories as lipid and 15% as protein) for 18 days, with isocaloric replacement of carbohydrate (46% of calories) by either ethanol or additional fat. The latter resulted in a high fat diet, with 82% of calories as lipid. After about 1 wk of alcohol, massive and persistent ketonuria developed. Compared with the control period, there was a 30-fold increase in fasting blood acetoacetate and beta-hydroxybutyrate (P < 0.001). With the high fat diet, acetoacetate and beta-hydroxybutyrate increased 8- to 10-fold (P < 0.001). In the postprandial state, ethanol also induced hyperketonemia, but less markedly than when ethanol followed an overnight fast. With low fat diets (5% of calories), alcohol (46% of total calories) did not induce ketonuria or hyperketonemia, suggesting that a combination of alcohol and dietary fat is necessary. The addition of alcohol to rat liver slices did not affect ketogenesis. In rats pretreated with alcohol for 3 days, however, ketonemia developed, hepatic glycogen was decreased, and liver slices (incubated with palmitate-(14)C and glucose) had a significant increase in acetoacetate production, when compared to carbohydrate pretreated controls. Alcohol pretreatment or addition of alcohol in vitro had no effect on acetoacetate utilization by rat diaphragms, and decreased only slightly the conversion of beta-hydroxybutyrate-(14)C to (14)CO(2). Thus, the hyperketonemia and ketonuria observed after alcohol consumption cannot be attributed to an immediate effect of alcohol, but is the consequence of a delayed change in intermediary metabolism characterized by increased hepatic ketone production from fatty acids, possibly linked to ethanol-induced glycogen depletion and depression of citric acid cycle activity.

摘要

在酗酒者中已观察到酮尿症。为研究这种效应的机制,健康志愿者接受了18天的充足饮食(热量的36%来自脂质,15%来自蛋白质),用乙醇或额外的脂肪等热量替代碳水化合物(热量的46%)。后者导致了高脂肪饮食,热量的82%来自脂质。饮用乙醇约1周后,出现了大量且持续的酮尿症。与对照期相比,空腹血中乙酰乙酸和β-羟基丁酸增加了30倍(P<0.001)。采用高脂肪饮食时,乙酰乙酸和β-羟基丁酸增加了8至10倍(P<0.001)。在餐后状态下,乙醇也会诱发高酮血症,但不如乙醇在空腹过夜后诱发的明显。采用低脂肪饮食(热量的5%)时,乙醇(占总热量的46%)不会诱发酮尿症或高酮血症,这表明乙醇和膳食脂肪的共同作用是必要的。向大鼠肝切片中添加乙醇不影响酮体生成。然而,在用乙醇预处理3天的大鼠中,出现了酮血症,肝糖原减少,并且与用碳水化合物预处理的对照组相比,肝切片(与棕榈酸 -(14)C和葡萄糖一起孵育)的乙酰乙酸生成显著增加。乙醇预处理或体外添加乙醇对大鼠膈肌利用乙酰乙酸没有影响,并且仅略微降低了β-羟基丁酸 -(14)C向(14)CO₂的转化。因此,饮酒后观察到的高酮血症和酮尿症不能归因于乙醇的直接作用,而是中间代谢延迟变化的结果,其特征是肝脏从脂肪酸生成酮体增加,这可能与乙醇诱导的糖原耗竭和柠檬酸循环活性降低有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9469/322666/5790e9e56761/jcinvest00226-0022-a.jpg

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