Differential toxicities of TCDD in vivo among normal, c-src knockout, geldanamycin- and quercetin-treated mice

被引:18
作者
Dunlap, DY
Moreno-Aliaga, MJ
Wu, Z
Matsumura, F
机构
[1] Univ Calif Davis, Dept Environm Toxicol, Davis, CA 95616 USA
[2] Univ Calif Davis, Environm Hlth Sci Ctr, Davis, CA 95616 USA
关键词
c-src knockout mice; 2,3,7,8-tetrachlorodibenzo-p-dioxin; differential toxicity; liver triglyceride accumulation;
D O I
10.1016/S0300-483X(99)00054-2
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Although we have previously reported the result of our preliminary study on the reduced toxic effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) in vivo in male c-src deficient, -/+ B6, 129-src(tmlSor) mice as compared to those in wild-type mice, there are still two major shortcomings off the above study: (a) the low number of individuals tested, (b) in some of the comparison tests, C57DL/6J mice (i.e. inbred B6 mice) were used as wild-type control mice. Since then we increased our laboratory breeding program and thereby the availability of B6, 129 -/+, -/- and true littermate wild-type +/+ individual mice. The results of critical in vivo toxicity comparison tests, involving 6-13 mice per test group, showed that there are considerable variations expressed in toxicity within each group of c-src deficient mice. Nevertheless, when a large enough number of individuals were tested two toxic effects were found to be less expressed in src-deficient mice. They were: (a) excess fatty deposits and (b) the mottled appearance of the liver which were commonly observed in TCDD-treated wild type mice, but not in c-src deficient mice. The former trend was also confirmed by both liver lipid analysis and histological examinations of the affected livers. As for the biochemical parameters, the hepatic nuclear protein binding to C/EBP (CCAAT/enhancer binding protein) response element appears to be uniformly reduced by the action of TCDD in +/+ mice, but not in -/+ or -/- mice. (C) 1999 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:95 / 107
页数:13
相关论文
共 25 条
[1]  
AIYER RA, 1990, LYMPHOKINE RES, V9, P333
[2]  
Ashida H, 1998, J BIOCHEM MOL TOXIC, V12, P191, DOI 10.1002/(SICI)1099-0461(1998)12:4<191::AID-JBT1>3.0.CO
[3]  
2-G
[4]   Population expansion, clonal growth, and specific differentiation patterns in primary cultures of hepatocytes induced by HGF/SF, EGF and TGF alpha in a chemically defined (HGM) medium [J].
Block, GD ;
Locker, J ;
Bowen, WC ;
Petersen, BE ;
Katyal, S ;
Strom, SC ;
Riley, T ;
Howard, TA ;
Michalopoulos, GK .
JOURNAL OF CELL BIOLOGY, 1996, 132 (06) :1133-1149
[5]  
Bock K W, 1994, Rev Physiol Biochem Pharmacol, V125, P1, DOI 10.1007/BFb0030908
[6]  
BUTLER WM, 1961, J LIPID RES, V2, P95
[7]   ACCURATE TRANSCRIPTION INITIATION BY RNA POLYMERASE-II IN A SOLUBLE EXTRACT FROM ISOLATED MAMMALIAN NUCLEI [J].
DIGNAM, JD ;
LEBOVITZ, RM ;
ROEDER, RG .
NUCLEIC ACIDS RESEARCH, 1983, 11 (05) :1475-1489
[8]   Role of CYP1A2 in hepatic sequestration of dioxin: Studies using CYP1A2 knock-out mice [J].
Diliberto, JJ ;
Burgin, D ;
Birnbaum, LS .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 236 (02) :431-433
[9]   Identification of c-Src as the integral component of the cytosolic Ah receptor complex, transducing the signal of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) through the protein phosphorylation pathway [J].
Enan, E ;
Matsumura, F .
BIOCHEMICAL PHARMACOLOGY, 1996, 52 (10) :1599-1612
[10]   ACTIVATION OF TRANSCRIPTION AS A GENERAL MECHANISM OF 2,3,7,8-TETRACHLORODIBENZO-P-DIOXIN ACTION [J].
FISHER, JM ;
JONES, KW ;
WHITLOCK, JP .
MOLECULAR CARCINOGENESIS, 1989, 1 (04) :216-221