Estrogens are known to protect postmenopausal women from heart disease. An extraordinary range of beneficial effects have been associated with estrogens and the range of mechanisms appear to be equally broad. One overlooked mechanism of estrogen protection is its function as an antioxidant. We have established that estrogen selectively protects high density lipoprotein (LDL) from oxidation in vitro and have preliminary evidence that his mechanism is operational in vivo. The antioxidant protection of HDL is predicted to preserve the antiatherogenic functions of HDL. A mechanism for this selective antioxidant protection of HDL is proposed and will be tested. Furthermore, we hypothesize that estrogen protects from oxidant stress at the cellular level, reducing the inflammatory response to oxidized lipids. To establish the importance of antioxidant actions of strong we propose to 1) confirm that a direct relationship exists between estrone-mediated anti antioxidant protection of HDL seen in vitro is operational in vivo; 3) test the hypothesis that estrogen modulates inflammatory components of atherosclerosis by inhibiting lipid peroxidation and stimulating an autoimmune response. Successful completion of the proposed studies will enhance our understanding of the mechanism of action of estrogens in protecting from heart disease and will contribute useful information for the design of therapeutic selective estrogen receptor modulators (SERMs).

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
2R01HL055517-04
Application #
2911089
Study Section
Biochemical Endocrinology Study Section (BCE)
Project Start
1996-08-01
Project End
2000-09-15
Budget Start
1999-09-15
Budget End
2000-09-15
Support Year
4
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Scripps Research Institute
Department
Type
DUNS #
City
La Jolla
State
CA
Country
United States
Zip Code
92037
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