Dehydroepiandrosterone suppresses the elevated hepatic glucose-6-phosphatase and fructose-1,6-bisphosphatase activities in C57BL/Ksj-db/db mice -: Comparison with troglitazone

被引:50
作者
Aoki, K [1 ]
Saito, T [1 ]
Satoh, S [1 ]
Mukasa, K [1 ]
Kaneshiro, M [1 ]
Kawasaki, S [1 ]
Okamura, A [1 ]
Sekihara, H [1 ]
机构
[1] Yokohama City Univ, Sch Med, Dept Internal Med 3, Kanazawa Ku, Yokohama, Kanagawa 2360004, Japan
关键词
D O I
10.2337/diabetes.48.8.1579
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The effect of dehydroepiandrosterone (DHEA) on the hepatic and muscle glucose metabolizing enzymes and on blood glucose were investigated in insulin-resistant diabetic C57BL/KsJ-db/db mice and their heterozygote littermates (db/+m). The results were compared with those after troglitazone administration under the same conditions. Despite hyperinsulinemia, hepatic glucose-6-phosphatase (G6Pase) and fructose-1,6-bisphosphatase (FBPase) activities are higher in db/db than in db/+m mice. Dietary administration of DHEA and that of troglitazone for 15 days to respective groups of five mice each significantly decreased blood glucose in db/db mice and hepatic G6Pase and FBPase activities in both db/db and db/+m mice, Hepatic G6Pase and FBPase activities showed a linear relationship with blood glucose in all groups of mice, suggesting that the activities of G6Pase and FBPase are closely related to blood glucose levels. Because androstenedione, a DHEA metabolite, barely affected either of these enzyme activities or blood glucose in db/db mice, the actions of DHEA, which are similar to those of troglitazone, are presumed to be caused by DHEA itself. DHEA is considered to be a modulating agent for the activities of hepatic gluconeogenic enzymes in db/db mice.
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页码:1579 / 1585
页数:7
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共 35 条
[1]  
BERDANIER CD, 1989, P SOC EXP BIOL MED, V192, P242, DOI 10.3181/00379727-192-42992
[2]  
BLAIR JB, 1976, J BIOL CHEM, V251, P3756
[3]   HEPATIC-METABOLISM OF GENETICALLY DIABETIC (DB-DB) MICE .1. CARBOHYDRATE-METABOLISM [J].
CHAN, TM ;
YOUNG, KM ;
HUTSON, NJ ;
BRUMLEY, FT ;
EXTON, JH .
AMERICAN JOURNAL OF PHYSIOLOGY, 1975, 229 (06) :1702-1712
[4]   ABNORMALITIES IN HEPATIC ENZYME ACTIVITIES DURING DEVELOPMENT OF DIABETES IN DB MICE [J].
CHANG, AY ;
SCHNEIDER, DI .
DIABETOLOGIA, 1970, 6 (03) :274-+
[5]  
CLEARY MP, 1991, P SOC EXP BIOL MED, V196, P8
[6]   EFFECT OF DEHYDROEPIANDROSTERONE TREATMENT ON LIVER-METABOLISM IN RATS [J].
CLEARY, MP .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY, 1990, 22 (03) :205-210
[7]   EFFECT OF GENETIC BACKGROUND ON THE THERAPEUTIC EFFECTS OF DEHYDROEPIANDROSTERONE (DHEA) IN DIABETES-OBESITY MUTANTS AND IN AGED NORMAL MICE [J].
COLEMAN, DL ;
SCHWIZER, RW ;
LEITER, EH .
DIABETES, 1984, 33 (01) :26-32
[8]   THERAPEUTIC EFFECTS OF DEHYDROEPIANDROSTERONE (DHEA) IN DIABETIC MICE [J].
COLEMAN, DL ;
LEITER, EH ;
SCHWIZER, RW .
DIABETES, 1982, 31 (09) :830-833
[9]   PHOSPHOENOLPYRUVATE CARBOXYKINASE (GUANOSINE TRIPHOSPHATE) FROM RAT-LIVER CYTOSOL - SEPARATION OF HOMOGENEOUS FORMS OF ENZYME WITH HIGH AND LOW ACTIVITY BY CHROMATOGRAPHY ON AGAROSE-HEXANE-GUANOSINE TRIPHOSPHATE [J].
COLOMBO, G ;
CARLSON, GM ;
LARDY, HA .
BIOCHEMISTRY, 1978, 17 (25) :5321-5329
[10]   SUPPRESSION OF HEPATIC GLUCONEOGENESIS IN LONG-TERM TROGLITAZONE TREATED DIABETIC KK AND C57BL/KSJ-DB/DB MICE [J].
FUJIWARA, T ;
OKUNO, A ;
YOSHIOKA, S ;
HORIKOSHI, H .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1995, 44 (04) :486-490