An increase in the plasma level of Hcy (homocysteine), an intermediate in the catabolism of methionine, has been identified as a risk factor for many diseases including CVD (cardiovascular disease). CVD is the major cause of death in patients with diabetes mellitus. Therefore the study of Hcy metabolism in diabetes mellitus has been a major focus of current research. Studies conducted in our laboratory were able to show that in both Type 1 and Type 2 diabetes with no renal complications, the plasma Hcy levels were lower than in controls. In Type 1 diabetes, increased activities of the trans-sulfuration enzymes were the major cause for the reduction in plasma Hcy. In Type 2 diabetes, BHMT (betaine:homocysteine methyltransferase) was also observed to play a major role in the increased catabolism of Hcy in addition to the trans-sulfuration enzymes. We were also able to demonstrate the direct effect of insulin and the counter-regulatory hormones on the regulation of cystathionine β-synthase and BHMT, which accounts for the changes in the activities of these two enzymes seen in diabetes mellitus.
Skip Nav Destination
Article navigation
November 2007
- Cover Image
- PDF Icon PDF LinkFront Matter
- PDF Icon PDF LinkTable of Contents
Conference Article|
October 25 2007
Homocysteine metabolism in diabetes
E.P. Wijekoon;
E.P. Wijekoon
1Department of Biochemistry, Memorial University of Newfoundland, St. John's, NL, Canada A1B 3X9
Search for other works by this author on:
M.E. Brosnan;
M.E. Brosnan
1Department of Biochemistry, Memorial University of Newfoundland, St. John's, NL, Canada A1B 3X9
Search for other works by this author on:
J.T. Brosnan
J.T. Brosnan
1
1Department of Biochemistry, Memorial University of Newfoundland, St. John's, NL, Canada A1B 3X9
1To whom correspondence should be addressed (email jbrosnan@mun.ca).
Search for other works by this author on:
Biochem Soc Trans (2007) 35 (5): 1175–1179.
Article history
Received:
June 11 2007
Citation
E.P. Wijekoon, M.E. Brosnan, J.T. Brosnan; Homocysteine metabolism in diabetes. Biochem Soc Trans 1 November 2007; 35 (5): 1175–1179. doi: https://doi.org/10.1042/BST0351175
Download citation file:
Sign in
Don't already have an account? Register
Sign in to your personal account
You could not be signed in. Please check your email address / username and password and try again.
Could not validate captcha. Please try again.