Ascorbic acid is a very good antioxidant found at high levels in many tissues, including ocular tissues, in comparison to plasma levels. It is involved in many physiological chemical reactions in which it is subsequently oxidized to a compound known as dehydroascorbic acid (DHAA) which, if allowed to accumulate, may be toxic. In normal, healthy tissues, DHAA generally appears to be recycled back to ascorbic acid. The suggestion has been made that the maintenance of a high ratio of ascorbic acid to DHAA in a particular tissue may be an indication of the health of that tissue. A recycling between the oxidized and reduced forms of the vitamin is absolutely necessary for maintaining a normally high ratio. The physiological mechanisms for recycling and the consequences of impaired recycling are not clearly understood and may be much more important than has been generally believed. The long term goal of this research project is to explain the overall role of vitamin C in maintaining normal physiological function at the cellular and subcellular level. The investigation will include the development of an understanding of physiological, biochemical, and molecular factors pertaining to specific mechanism(s) of normal vitamin C metabolism, causes of abnormal metabolism observed in stressed conditions, and the consequences of an impaired handling of the vitamin for oxidative and other physiological processes within the cell.
Specific aims are to 1) identify and evaluate the enzymatic mechanism(s) by which ascorbic acid is maintained in its useful; nontoxic reduced form in mammalian tissues, including ocular tissues; 2) investigate the significance of processes that influence the steady state ratio of AA/DHAA; and 3) determine the role and regulation of protein-related recycling mechanisms under normal and diabetic (hyperglycemic) conditions.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
First Independent Research Support & Transition (FIRST) Awards (R29)
Project #
5R29DK047953-06
Application #
2856772
Study Section
Nutrition Study Section (NTN)
Program Officer
May, Michael K
Project Start
1995-01-01
Project End
1999-12-31
Budget Start
1999-04-15
Budget End
1999-12-31
Support Year
6
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of Oregon
Department
Miscellaneous
Type
Schools of Arts and Sciences
DUNS #
948117312
City
Eugene
State
OR
Country
United States
Zip Code
97403
Ren, J; Bode, A M (2000) Altered cardiac excitation-contraction coupling in ventricular myocytes from spontaneously diabetic BB rats. Am J Physiol Heart Circ Physiol 279:H238-44
Bode, A M; Rose, R C (1999) Analysis of water-soluble antioxidants by high-performance liquid chromatography with electrochemical detection. Methods Enzymol 299:77-83
Vethanayagam, J G; Green, E H; Rose, R C et al. (1999) Glutathione-dependent ascorbate recycling activity of rat serum albumin. Free Radic Biol Med 26:1591-8
Rose, R C; Richer, S P; Bode, A M (1998) Ocular oxidants and antioxidant protection. Proc Soc Exp Biol Med 217:397-407