INVIVO AND INVITRO EVIDENCE CONCERNING THE ROLE OF LIPID-PEROXIDATION IN THE MECHANISM OF HEPATOCYTE DEATH DUE TO CARBON-TETRACHLORIDE

被引:58
作者
BIASI, F
ALBANO, E
CHIARPOTTO, E
CORONGIU, FP
PRONZATO, MA
MARINARI, UM
PAROLA, M
DIANZANI, MU
POLI, G
机构
[1] UNIV TURIN,DEPT EXPTL MED & ONCOL,C SO RAFFAELLO 30,I-10125 TURIN,ITALY
[2] UNIV CAGLIARI,DEPT EXPTL BIOL,I-09100 CAGLIARI,ITALY
[3] UNIV GENOA,INST GEN PATHOL,I-16132 GENOA,ITALY
关键词
LIPID PEROXIDATION; CARBON TETRACHLORIDE; HEPATOCYTE DEATH; INTRACELLULAR CALCIUM;
D O I
10.1002/cbf.290090208
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Isolated rat hepatocytes exposed to CCl4 showed a stimulated formation of malonaldehyde after only 30-60 min incubation. Conversely, the onset of hepatocyte death was a relatively late event, being significant only after 2-3 h of treatment. A cause-effect relationship between the two phenomena has been demonstrated by using hepatocytes isolated from rats pretreated with alpha-tocopherol. Comparable results were obtained in vivo where supplementation with alpha-tocopherol 15 h before CCl4 dosing induced a partial or complete protection against the drug's necrogenic effect, depending on the concentration of the haloalkane used. Moreover, the vitamin supplementation prevented the CCl4-induced increase of liver total calcium content, probably by blocking alterations in the liver cell plasma membranes due to lipid peroxidation.
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页码:111 / 118
页数:8
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