Lipid autoxidation, which results in the formation of hydroperoxides and secondary products, has been implicated in many degenerative diseases, such as atherosclerosis. In order to more fully understand the role of lipid autoxidation in the progression of such diseases, as well as treatment, knowledge of the fundamental chemistry that is occurring is necessary. This research project. is designed to investigate the formation and reactivity of bis-allylic lipid hydroperoxides, which have only recently been identified as products of lipid autoxidation. The tools and theories of organic chemistry, such as synthesis, isotopic labelling experiments, and a new HPLC/Ag-CIS-MS (Ag coordination ionspray mass spectrometry) method will be utilized to investigate the reactivity of the hydroperoxide. This powerful and mild method allows potentially labile, neutral compounds to be analyzed and identified without significant manipulation of the sample. The reactivity of the bis-allylic hydroperoxide in the presence of various anti-oxidants, mechanism and kinetics of formation and rearrangement, and potential biological relevance are the focus of this research.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
1F32HL068439-01
Application #
6406596
Study Section
Bio-Organic and Natural Products Chemistry Study Section (BNP)
Program Officer
Schucker, Beth
Project Start
2001-09-30
Project End
Budget Start
2001-09-30
Budget End
2002-09-29
Support Year
1
Fiscal Year
2001
Total Cost
$34,832
Indirect Cost
Name
Vanderbilt University Medical Center
Department
Biochemistry
Type
Schools of Medicine
DUNS #
004413456
City
Nashville
State
TN
Country
United States
Zip Code
37212
Tallman, Keri A; Roschek Jr, Bill; Porter, Ned A (2004) Factors influencing the autoxidation of fatty acids: effect of olefin geometry of the nonconjugated diene. J Am Chem Soc 126:9240-7