Plasma homocysteine level and hepatic sulfur amino acid metabolism in mice fed a high-fat diet

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Title
Plasma homocysteine level and hepatic sulfur amino acid metabolism in mice fed a high-fat diet
Author(s)
K U Yun; C S Ryu; J M Oh; C H Kim; K S Lee; Chul Ho LeeHyun Sun Lee; B H Kim; S K Kim
Bibliographic Citation
European Journal of Nutrition, vol. 52, no. 1, pp. 127-134
Publication Year
2013
Abstract
Purpose: Obesity, a feature of metabolic syndrome, is a risk factor for cardiovascular disease, and elevated plasma homocysteine is associated with increased cardiovascular risk. However, little published information is available concerning the effect of obesity on homocysteine metabolism. Methods: Hepatic homocysteine metabolism was determined in male C57BL/6 mice fed a high-fat diet for 12 weeks. Results: High-fat diet increased plasma homocysteine but decreased hepatic homocysteine levels. Hepatic S-adenosylhomocysteine hydrolase levels were down-regulated in the obese mice, which was in part responsible for the decrease in hepatic S-adenosylmethionine/S- adenosylhomocysteine, which served as an index of transmethylation potential. Despite the decrease in hepatic cysteine, hepatic taurine synthesis was activated via up-regulation of cysteine dioxygenase. Hepatic levels of methionine adenosyltransferase I/III, methionine synthase, methylene tetrahydrofolate reductase, and gamma-glutamylcysteine ligase catalytic subunit were unchanged. Obese mice showed elevated betaine-homocysteine methyltransferase and decreased cystathionine beta-synthase activities, although the quantities of these enzymes were unchanged. Conclusion: This study suggests that plasma homocysteine level is increased in obesity-associated hepatic steatosis, possibly as a result of increased hepatic homocysteine efflux along with an altered sulfur amino acid metabolism.
Keyword
Hepatic steatosisHigh-fat dietHomocysteineObesitySulfur amino acid metabolism
ISSN
1436-6207
Publisher
Springer
DOI
http://dx.doi.org/10.1007/s00394-011-0294-0
Type
Article
Appears in Collections:
Ochang Branch Institute > Division of Bioinfrastructure > Laboratory Animal Resource Center > 1. Journal Articles
Ochang Branch Institute > Natural Medicine Research Center > 1. Journal Articles
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