Gender-related difference in altered gene expression of a sterol regulatory element binding protein, SREBP-2, by lead nitrate in rats: Correlation with development of hypercholesterolemia

被引:6
作者
Kojima, Misaki
Degawa, Masakuni
机构
[1] Natl Inst Agrobiol Sci, Inst Insect & Anim Sci, Dept Physiol & Genet Regulat, Lab Anim Gene Funct, Tsukuba, Ibaraki 3058602, Japan
[2] Univ Shizuoka, Dept Mol Toxicol, Shizuoka 4228526, Japan
[3] Univ Shizuoka, Sch Pharmaceut Sci, COE Program 21st Century, Shizuoka 4228526, Japan
关键词
lead nitrate; sterol regulatory element binding protein-2; HMG-CoA reductase; cholesterol; sex-difference; rat;
D O I
10.1002/jat.1138
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Changes in gene expression levels of hepatic sterol regulatory element binding protein-2 (SREBP-2) and 3-hydroxy-3-methylglutaryl-CoA reductase (HMGR) after a single i.v. injection of lead nitrate (LN, 100 mu mol kg(-1) body weight) were examined comparatively by real time reverse transcriptase-polymerase chain reaction (RT-PCR) in male and female rats. Significant increases in the gene expression level of SREBP-2, a transcription factor for the HMGR gene, occurred at 6-12 h in male and at 24-36 h in female rats after LN-treatment. The gene expression level of HMGR, a rate-limiting enzyme for cholesterol biosynthesis, significantly increased at 3-48 h in male rats and 12-48 h in female rats. Subsequently, significant increases in the amount of hepatic total cholesterol in male and female rats were also observed at 3-48 h and 24-48 h, respectively. The present findings demonstrate that increases in gene expressions of hepatic SREBP-2 and HMGR and the amount of hepatic total cholesterol by LN occur earlier in male rats than in the females, and that increases in the gene expression level of HMGR and the amount of hepatic total cholesterol occur prior to the increase in the gene expression level of SREBP-2 in either sex of rats. Copyright (c) 2006 John Wiley & Sons, Ltd.
引用
收藏
页码:381 / 384
页数:4
相关论文
共 20 条
[1]   The SREBP pathway: Regulation of cholesterol metabolism by proteolysis of a membrane-bound transcription factor [J].
Brown, MS ;
Goldstein, JL .
CELL, 1997, 89 (03) :331-340
[2]   SEX-DIFFERENCE IN THE AGE-RELATED CHANGE OF CHOLESTEROL-METABOLISM IN RATS [J].
CHOI, YS ;
SUGANO, M ;
IDE, T .
MECHANISMS OF AGEING AND DEVELOPMENT, 1988, 44 (01) :91-99
[3]   PREFERENTIAL INHIBITIONS OF HEPATIC P450IA2 EXPRESSION AND INDUCTION BY LEAD NITRATE IN THE RAT [J].
DEGAWA, M ;
ARAI, H ;
MIURA, S ;
HASHIMOTO, Y .
CARCINOGENESIS, 1993, 14 (06) :1091-1094
[4]   HEPATIC CHOLESTEROL IN LEAD NITRATE INDUCED LIVER HYPERPLASIA [J].
DESSI, S ;
BATETTA, B ;
LACONI, E ;
ENNAS, C ;
PANI, P .
CHEMICO-BIOLOGICAL INTERACTIONS, 1984, 48 (03) :271-279
[5]   HEPATIC HYDROXYMETHYLGLUTARYL COENZYME-A REDUCTASE-ACTIVITY IN INBRED STRAINS OF MICE [J].
DUPONT, J ;
AUBERT, R ;
KUAN, SI ;
WARNER, DA ;
CAMUS, MC ;
HERZOG, J .
ENZYME, 1988, 40 (04) :198-203
[6]   Low-level lead-induced neurotoxicity in children: an update on central nervous system effects [J].
Finkelstein, Y ;
Markowitz, ME ;
Rosen, JF .
BRAIN RESEARCH REVIEWS, 1998, 27 (02) :168-176
[7]  
FOLCH J, 1957, J BIOL CHEM, V226, P497
[8]   FERTILITY OF MALE WORKERS EXPOSED TO CADMIUM, LEAD, OR MANGANESE [J].
GENNART, JP ;
BUCHET, JP ;
ROELS, H ;
GHYSELEN, P ;
CEULEMANS, E ;
LAUWERYS, R .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1992, 135 (11) :1208-1219
[9]   REGULATION OF THE MEVALONATE PATHWAY [J].
GOLDSTEIN, JL ;
BROWN, MS .
NATURE, 1990, 343 (6257) :425-430
[10]   LEAD TOXICITY - CURRENT CONCERNS [J].
GOYER, RA .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1993, 100 :177-187