alpha-Glutathione s-transferase (alpha-GST) release, an early indicator of carbon tetrachloride hepatotoxicity in the rat

被引:33
作者
Clarke, H
Egan, DA
Heffernan, M
Doyle, S
Byrne, C
Kilty, C
Ryan, MP
机构
[1] NATL UNIV IRELAND UNIV COLL DUBLIN,DEPT PHARMACOL,DUBLIN 4,IRELAND
[2] BIOTRIN INT,DUBLIN,IRELAND
来源
HUMAN & EXPERIMENTAL TOXICOLOGY | 1997年 / 16卷 / 03期
关键词
alpha glutathione s-transferase; alpha-GST; aspartate amino-transferase; AST; hepatotoxicity; carbon tetrachloride; biomarker;
D O I
10.1177/096032719701600304
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
1 The use of the cytoplasmic enzyme, alpha glutathione s-transferase (alpha-GST) as an early index of carbon tetrachloride (CCl4) toxicity in the rat was investigated and compared with a standard enzyme marker, aspartate aminotransferase (AST). The hepatotoxic effects of CCl4 in the rat were determined in a time and dose-response study. 2 Following CCl4 exposure, alpha-GST release was shown to be an earlier and more sensitive biomarker of hepatotoxicity than AST. 3 Significant increases in alpha-GST were detected 2 h after CCl4 exposure. Using the enzyme marker AST, this early hepatotoxic injury went undetected. At 6 and 16 h, alpha-GST was also a more sensitive indicator of hepatotoxicity than AST. 4 alpha-GST release was significantly increased at a dose of 5 mu l/kg, the lowest concentration of CCl4 administered and clearly responded in a dose-dependent manner with increasing doses of CCl4. In contrast, release of AST did not reach statistical significance until a dose of 25 mu l/kg. 5 Thus, these findings indicate that alpha-GST is a more sensitive and more accurate reflector of CCl4 induced hepatotoxicity than AST.
引用
收藏
页码:154 / 157
页数:4
相关论文
共 22 条
[1]   GLUTATHIONE-RELATED ENZYME-ACTIVITIES IN TESTIS OF PATIENTS WITH MALIGNANT DISEASES [J].
ACETO, A ;
DIILIO, C ;
ANGELUCCI, S ;
TENAGLIA, R ;
ZEZZA, A ;
CACCURI, AM ;
FEDERICI, G .
CLINICA CHIMICA ACTA, 1989, 183 (01) :83-86
[2]   PLASMA GLUTATHIONE S-TRANSFERASE MEASUREMENTS AFTER PARACETAMOL OVERDOSE - EVIDENCE FOR EARLY HEPATOCELLULAR DAMAGE [J].
BECKETT, GJ ;
CHAPMAN, BJ ;
DYSON, EH ;
HAYES, JD .
GUT, 1985, 26 (01) :26-31
[3]  
BECKETT GJ, 1989, CLIN CHEM, V35, P2186
[4]  
Beckett GJ, 1993, ADV CLIN CHEM, V30, P282
[5]  
CASARETT LJ, 1980, TOXICOLOGY BASIC SCI, P645
[6]  
FRIEDEN J, 1989, J ORTHOPAED RES, V7, P142
[7]   The glutathione S-Transferase supergene family: Regulation of GST and the contribution of the isoenzymes to cancer chemoprotection and drug resistance [J].
Hayes, JD ;
Pulford, DJ .
CRITICAL REVIEWS IN BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1995, 30 (06) :445-600
[8]  
HENRY RJ, 1960, AM J CLIN PATHOL, V34, P381
[9]   THE HUMAN GLUTATHIONINE S-TRANSFERASES - IMMUNOHISTOCHEMICAL STUDIES OF THE DEVELOPMENTAL EXPRESSION OF ALPHA-CLASS AND PI-CLASS ISOENZYMES IN LIVER [J].
HILEY, C ;
FRYER, A ;
BELL, J ;
HUME, R ;
STRANGE, RC .
BIOCHEMICAL JOURNAL, 1988, 254 (01) :255-259
[10]   IMPAIRED HEPATOCELLULAR INTEGRITY DURING GENERAL-ANESTHESIA, AS ASSESSED BY MEASUREMENT OF PLASMA GLUTATHIONE-S-TRANSFERASE [J].
HUSSEY, AJ ;
HOWIE, J ;
ALLAN, LG ;
DRUMMOND, G ;
HAYES, JD ;
BECKETT, GJ .
CLINICA CHIMICA ACTA, 1986, 161 (01) :19-28