Dehydroepiandrosterone suppresses elevated hepatic glucose-6-phosphatase mRNA level in C57BL/KsJ-db/db mice: Comparison with troglitazone

被引:18
作者
Aoki, K [1 ]
Kikuchi, T [1 ]
Mukasa, K [1 ]
Ito, S [1 ]
Nakajima, A [1 ]
Satoh, 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
DHEA; troglitazone; db/db mouse; glucose-6-phosphatase;
D O I
10.1507/endocrj.47.799
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Dehydroepiandrosterone (DHEA) is known to improve hyperglycemia of diabetic C57BL/KsJ-db/db mice that are obese and insulin resistant. In a previous study, we reported that DHEA as well as troglitazone suppress es the elevated hepatic gluconeogenic enzymes, glucose-6-phosphatase (G6Pase) and fructose-1,6-bisphosphatase (FBPase) activities in CS7BL/KsJ-db/db mice. In the present study, we evaluated the changes in mRNA of G6Pase and FBPase in db/db mice. Despite hyperinsulinemia, the G6Pase mRNA level of db/db mice was elevated as compared to their heterozygote littermate db/+m mice. In contrast, the FBPase mRNA level was not elevated in db/db mice. Administration of DHEA for two weeks significantly decreased the blood glucose level and the elevated G6Pase mRNA level in db/db mice. No significant changes were seen in the FBPase mRNA level after the administration of DHEA. Administration of troglitazone also decreased the blood glucose and G6Pase mRNA level in db/db mice although no changes were seen in the FBPase mRNA level. These results suggest that the elevation of G6Pase mRNA is important in elucidating the cause of insulin resistance, and that the G6Pase gene is at least one target for the hypoglycemic effects of DHEA as an insulin sensitizing agent in db/db mice.
引用
收藏
页码:799 / 804
页数:6
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