DIFFERENTIAL EXPRESSION OF HEPATIC ESTROGEN, PHENOL AND DEHYDROEPIANDROSTERONE SULFOTRANSFERASES IN GENETICALLY-OBESE DIABETIC (OB/OB) MALE AND FEMALE MICE

被引:13
作者
BORTHWICK, EB
BURCHELL, A
COUGHTRIE, MWH
机构
[1] UNIV DUNDEE, NINEWELLS HOSP & MED SCH, DEPT BIOCHEM MED, DUNDEE DD1 9SY, SCOTLAND
[2] UNIV DUNDEE, NINEWELLS HOSP & MED SCH, DEPT OBSTET & GYNAECOL, DUNDEE DD1 9SY, SCOTLAND
关键词
D O I
10.1677/joe.0.1440031
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Sulphotransferases (STs) are a family of closely related enzymes playing a key role in regulation of the bioavailability and activity of important endogenous molecules such as steroid hormones. A relationship between the expression of steroid STs and the diabetic state has been demonstrated in various laboratory animal models, and steroid sulphates such as dehydroepiandrosterane sulphate are known to have anti-diabetic properties. In order to further our understanding of the molecular basis for the association of steroid hormone sulphation and diabetes, we have examined the expression of oestrogen, phenol and dehydroepiandrosterone (DHEA) STs in mice carrying the obesity mutation (ob), which in the homozygous state (ob/ob) produces mice which are obese and diabetic. Our data show that, in male mice, ST activities towards oestrone (E(1)), oestriol (E(3)), DHEA and the xenobiotic 1-naphthol are elevated in ob/ob mice, whereas in female mice, only the oestrogen ST activities were elevated, with the DHEA and 1-naphthol ST activities reduced. Using antibodies directed against oestrogen ST, it was demonstrated that the induction of E(1) and E(3) ST activity in ob/ob mice correlated with the expression of an ST isoenzyme not constitutively expressed in control mouse liver.
引用
收藏
页码:31 / 37
页数:7
相关论文
共 36 条
[21]   OBESITY-INDUCED DIABETES (DIABESITY) IN C57BL/KSJ MICE PRODUCES ABERRANT TRANSREGULATION OF SEX STEROID SULFOTRANSFERASE GENES [J].
LEITER, EH ;
CHAPMAN, HD .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 93 (05) :2007-2013
[22]   SYNERGISM OF OBESITY GENES WITH HEPATIC-STEROID SULFOTRANSFERASES TO MEDIATE DIABETES IN MICE [J].
LEITER, EH ;
CHAPMAN, HD ;
FALANY, CN .
DIABETES, 1991, 40 (10) :1360-1363
[23]   THE INFLUENCE OF GENETIC BACKGROUND ON THE EXPRESSION OF MUTATIONS AT THE DIABETES LOCUS IN THE MOUSE .5. INTERACTION BETWEEN THE DB GENE AND HEPATIC SEX STEROID SULFOTRANSFERASES CORRELATES WITH GENDER-DEPENDENT SUSCEPTIBILITY TO HYPERGLYCEMIA [J].
LEITER, EH ;
CHAPMAN, HD ;
COLEMAN, DL .
ENDOCRINOLOGY, 1989, 124 (02) :912-922
[25]  
LOWRY OH, 1951, J BIOL CHEM, V193, P265
[26]  
NASH AR, 1988, AUST J BIOL SCI, V41, P507
[27]   MOLECULAR-CLONING AND EXPRESSION OF A FULL-LENGTH COMPLEMENTARY-DNA ENCODING THE GUINEA-PIG ADRENOCORTICAL ESTROGEN SULFOTRANSFERASE [J].
OEDA, T ;
LEE, YC ;
DRISCOLL, WJ ;
CHEN, HC ;
STROTT, CA .
MOLECULAR ENDOCRINOLOGY, 1992, 6 (08) :1216-1226
[28]   CDNA CLONING OF THE HYDROXYSTEROID SULFOTRANSFERASE STA SHARING A STRONG HOMOLOGY IN AMINO-ACID-SEQUENCE WITH THE SENESCENCE MARKER PROTEIN SMP-2 IN RAT LIVERS [J].
OGURA, K ;
KAJITA, J ;
NARIHATA, H ;
WATABE, T ;
OZAWA, S ;
NAGATA, K ;
YAMAZOE, Y ;
KATO, R .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 166 (03) :1494-1500
[29]  
OTTERNESS DM, 1992, MOL PHARMACOL, V41, P865
[30]   NUCLEOTIDE-SEQUENCE OF A FULL-LENGTH CDNA (PST-1) FOR ARYL SULFOTRANSFERASE FROM RAT-LIVER [J].
OZAWA, S ;
NAGATA, K ;
GONG, DW ;
YAMAZOE, Y ;
KATO, R .
NUCLEIC ACIDS RESEARCH, 1990, 18 (13) :4001-4001