STUDIES ON UREA SYNTHESIS IN THE LIVER OF RATS TREATED CHRONICALLY WITH ETHANOL USING PERFUSED LIVERS, ISOLATED HEPATOCYTES, AND MITOCHONDRIA

被引:14
作者
ADACHI, K
MATSUHASHI, T
NISHIZAWA, Y
USUKURA, J
POPINIGIS, J
WAKABAYASHI, T
机构
[1] NAGOYA UNIV, SCH MED, DEPT CELL BIOL & MOLEC PATHOL, SHOWA KU, NAGOYA, AICHI 466, JAPAN
[2] JEDRZEJ SNIADECKI ACAD PHYS EDUC, DEPT BIOENERGET, PL-80336 GDANSK, POLAND
关键词
CHRONIC ETHANOL INTOXICATION; HEPATIC MEGAMITOCHONDRIA; UREA SYNTHESIS; PERFUSED LIVERS; HEPATOCYTE; INTRACELLULAR ATP;
D O I
10.1016/0006-2952(95)02023-3
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Changes in urea synthesis in the liver of rats treated with 32% ethanol in the drinking water for up to 6 months were studied using perfused livers, isolated hepatocytes, and mitochondria. Results obtained from ethanol-treated rats are summarized as follows: (1) the mitochondria of the hepatocytes of rats treated with ethanol for 2 months or longer became enlarged to various degrees, (2) the levels of ammonia in the serum remained within a normal range, while those in liver tissue were elevated compared with the control, (3) urea synthesis from ammonia in perfused livers was decreased markedly, while that from citrulline remained in the normal range, (4) the activities of carbamyl phosphate synthetase (CPS; EC 2.7.2.5) and omithine transcarbamylase (OTC; EC 2.1.3.3) in mitochondria were unchanged compared with those of the control, and (5) the levels of ATP in liver tissue and the ability of mitochondria to synthesize ATP were decreased markedly compared with the control. Both the level of ATP in the hepatocytes and the synthesis of urea from ammonia by perfused livers of rats treated with ethanol were resistant to externally added ethanol, while those of control animals were severely affected. These results suggest that the intracellular level of ATP is intimately related to urea synthesis in both control and ethanol-treated animals, and lowered levels of ATP may be a key factor in the suppression of urea synthesis in ethanol-treated animals.
引用
收藏
页码:1391 / 1399
页数:9
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