Aging delays the post-necrotic restoration of liver function

被引:6
作者
Sanz, N [1 ]
Díez-Fernández, C [1 ]
Cascales, M [1 ]
机构
[1] Univ Complutense Madrid, Fac Farm, CSIC, Inst Bioquim, E-28040 Madrid, Spain
关键词
D O I
10.1002/biof.5520080118
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
Age-associated changes in liver injury and post-necrotic regeneration were studied in rats aged 6 and 30 months in a period of 96 h following a dose of thioacetamide (6.6 mmol/kg body weight). Hepatocellular necrosis was detected in both groups by serum aspartate aminotransferase, but the severity of injury was significantly lower (one fourth, p < 0.001) in the oldest. Differences were observed in hepatocyte FAD monooxygenase activity between 6 and 30 months old rats at 24 h (278 versus 170%, p < 0.001, respectively) and also in GSH/GSSG ratio, in protein thiol groups and in malondialdehyde. Glutathione. peroxidase, glutathione reductase and glucose-6-phosphate dehydrogenase activities rose markedly in both groups, this increase being slightly lower in the oldest. Superoxide dismutase and catalase did not show significant changes between both groups. At the end of the 96 h experimental period the restoration towards normal of GSG/GSSG, protein thiols malondialdehyde and the activities of Cu-Zn superoxide dismutase and catalase were significantly lower in hepatocytes from 30 months old rats. We summarize that the main age-related changes in the sequenced process of liver injury and regeneration occurred to a lesser extent in severity of injury and delayed response in the post-necrotic restoration of liver function, probably due to a lower increase in antioxidant enzyme system.Age-associated changes in liver injury and post-necrotic regeneration were studied in rats aged 6 and 30 months in a period of 96 h following a dose of thioacetamide (6.6 mmol/kg body weight). Hepatocellular necrosis was detected in both groups by serum aspartate aminotransferase, but the severity of injury was significantly lower (one fourth, p < 0.001) in the oldest. Differences were observed in hepatocyte FAD monooxygenase activity between 6 and 30 months old rats at 24 h (278 versus 170%, p < 0.001, respectively) and also in GSH/GSSG ratio, in protein thiol groups and in malondialdehyde. Glutathione. peroxidase, glutathione reductase and glucose-6-phosphate dehydrogenase activities rose markedly in both groups, this increase being slightly lower in the oldest. Superoxide dismutase and catalase did not show significant changes between both groups. At the end of the 96 h experimental period the restoration towards normal of GSG/GSSG, protein thiols malondialdehyde and the activities of Cu-Zn superoxide dismutase and catalase were significantly lower in hepatocytes from 30 months old rats. We summarize that the main age-related changes in the sequenced process of liver injury and regeneration occurred to a lesser extent in severity of injury and delayed response in the post-necrotic restoration of liver function, probably due to a lower increase in antioxidant enzyme system.
引用
收藏
页码:103 / 109
页数:7
相关论文
共 17 条
[1]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[2]   ROLE OF THE MICROSOMAL FAD-CONTAINING MONOOXYGENASE IN THE LIVER TOXICITY OF THIOACETAMIDE S-OXIDE [J].
CHIELI, E ;
MALVALDI, G .
TOXICOLOGY, 1984, 31 (01) :41-52
[3]  
Del Maestro R.F., 1983, OXYGEN RADICALS THEI, V2, P28
[4]   Intracellular calcium concentration impairment in hepatocytes from thioacetamide-treated rats. Implications for the activity of Ca2+-dependent enzymes [J].
DiezFernandez, C ;
Sanz, N ;
Cascales, M .
JOURNAL OF HEPATOLOGY, 1996, 24 (04) :460-467
[5]   RELATIONSHIP BETWEEN GENOMIC DNA-PLOIDY AND PARAMETERS OF LIVER-DAMAGE DURING NECROSIS AND REGENERATION INDUCED BY THIOACETAMIDE [J].
DIEZFERNANDEZ, C ;
BOSCA, L ;
FERNANDEZSIMON, L ;
ALVAREZ, A ;
CASCALES, M .
HEPATOLOGY, 1993, 18 (04) :912-918
[6]  
FERNANDEZCHECA JC, 1992, J BIOL CHEM, V267, P1667
[7]  
Katz Norbert, 1993, P55
[8]   AGING AND THE LIVER - FUNCTIONAL-ASPECTS [J].
KITANI, K .
ARCHIVES OF GERONTOLOGY AND GERIATRICS, 1994, 19 (02) :145-158
[9]   HEPATOCELLULAR REGENERATION - KEY TO THIOACETAMIDE AUTOPROTECTION [J].
MANGIPUDY, RS ;
CHANDA, S ;
MEHENDALE, HM .
PHARMACOLOGY & TOXICOLOGY, 1995, 77 (03) :182-188
[10]   NOVEL MECHANISMS IN CHEMICALLY-INDUCED HEPATOTOXICITY [J].
MEHENDALE, HM ;
ROTH, RA ;
GANDOLFI, AJ ;
KLAUNIG, JE ;
LEMASTERS, JJ ;
CURTIS, LR .
FASEB JOURNAL, 1994, 8 (15) :1285-1295