Effects of intravenous betaine on methionine-loading–induced plasma homocysteine elevation in rats

An intravenous methionine-loading model was characterized, and the suppressive effect of betaine on plasma homocysteine elevation induced by methionine loading was examined in rats. The plasma homocysteine concentrations significantly increased 5–120 minutes after 0.34 mmol/kg of methionine loading...

Full description

Saved in:
Bibliographic Details
Published inThe Journal of nutritional biochemistry Vol. 15; no. 11; pp. 666 - 671
Main Authors Yagisawa, Masako, Okawa, Nao, Shigematsu, Norihiro, Nakata, Rieko
Format Journal Article
LanguageEnglish
Published New York, NY Elsevier Inc 01.11.2004
Elsevier Science
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:An intravenous methionine-loading model was characterized, and the suppressive effect of betaine on plasma homocysteine elevation induced by methionine loading was examined in rats. The plasma homocysteine concentrations significantly increased 5–120 minutes after 0.34 mmol/kg of methionine loading and then returned to the baseline within 240 minutes. Betaine was then intravenously administered at the same time as the methionine loading. The total increment of plasma homocysteine was assessed using the positive incremental area under the plasma homocysteine concentration curve over the 240-minute post–methionine-loading period (ΔAUC 0-240). Betaine reduced ΔAUC 0-240 dose-dependently: 81% of the control by 1.7 mmol/kg of betaine and 33% by 3.4 mmol/kg. The effects of glycine and methylglycine, analogues of betaine, were also investigated. As observed for betaine, methylglycine decreased ΔAUC 0-240 to 44% of the control, whereas glycine showed no significant effect on ΔAUC 0-240, indicating that methyl groups of betaine and dimethylglycine were necessary to suppress plasma homocysteine elevation. These results suggest that betaine contributes to the suppression of plasma homocysteine elevation by promoting homocysteine metabolism, and seems to work as a methyl donor.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0955-2863
1873-4847
DOI:10.1016/j.jnutbio.2004.05.004