The long-term objectives of the project are to establish the site and mechanism of action of the two mutations diabetes (db) and obese (ob) that cause severe and rapidly developing diabetes-obesity syndromes in mice and to compare the metabolic alterations observed in these mutants with other single gene mutations that cause similar but milder obesity conditions.
The specific aims of this application are to assess and define the mode of action of the adrenal androgen, dehydroepiandrosterone (DHEA) and its metabolites in producing the marked beneficial effects on both these syndromes and to establish how much the deranged hormonal milieu associated with mutants contributes to increased metabolic efficiency by preventing normal metabolic turnover of tissue. Whether DHEA acts a modulator that can restore a more normal hormonal balance will be assessed. The effects of the inbred background both on the expression of these syndromes and on the therapeutic effects of DHEA and its metabolites will be studied in the hopes of identifying specific genetic modifiers involved in the differing strain responses. An understanding of the mode of action of these new anti-diabetic agents and their interaction with different forms of genetic diabetes should provide new information regarding glucose homestasis, factors regulating beta cell replication, and could provide data that would suggest the primary lesion in each syndrome. Once the most effect dosages and the toxicity are established, these new oral hypoglycemic agents may become significant in the treatment of human diabetes. Two metabolites of DHEA, Alpha- and Beta-etiocholanolone, have been found more therapeutic than DHEA itself. These etiocholanolones have always been considered as end-products of steroid metabolism with no known biological functions. My studies using the etiocholanolones in treating various types of diabetes-obesity syndromes suggest that these compounds may be metabolic effectors in their own right and may prove to be safe and effective oral agents in the control of diabetes and obesity conditions.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
2R01DK014461-17
Application #
3225224
Study Section
Mammalian Genetics Study Section (MGN)
Project Start
1975-05-01
Project End
1991-04-30
Budget Start
1986-05-01
Budget End
1987-04-30
Support Year
17
Fiscal Year
1986
Total Cost
Indirect Cost
Name
Jackson Laboratory
Department
Type
DUNS #
042140483
City
Bar Harbor
State
ME
Country
United States
Zip Code
04609