Dietary vitamin B-6 restriction does not alter rates of homocysteine remethylation or synthesis in healthy young women and men

Am J Clin Nutr. 2005 Mar;81(3):648-55. doi: 10.1093/ajcn/81.3.648.

Abstract

Background: The effects of vitamin B-6 status on steady-state kinetics of homocysteine metabolism in humans are unclear.

Objective: The objective was to determine the effects of dietary vitamin B-6 restriction on the rates of homocysteine remethylation and synthesis in healthy humans.

Design: Primed, constant infusions of [(13)C(5)]methionine, [3-(13)C]serine, and [(2)H(3)]leucine were conducted in healthy female (n=5) and male (n=4) volunteers (20-30 y) before and after 4 wk of dietary vitamin B-6 restriction (<0.5 mg vitamin B-6/d) to establish whether vitamin B-6 status affects steady-state kinetics of homocysteine metabolism in the absence of concurrent methionine intake. Effects of dietary vitamin B-6 restriction on vitamin B-6 status, plasma amino acid concentrations, and the rates of reactions of homocysteine metabolism were assessed.

Results: Dietary vitamin B-6 restriction significantly reduced plasma pyridoxal 5-phosphate (PLP) concentrations (55.1 +/- 8.3 compared with 22.6 +/- 1.3 nmol/L; P=0.004), significantly increased plasma glycine concentrations (230 +/- 14 compared with 296 +/- 15; P=0.008), and significantly reduced basal (43%; P < 0.001) and PLP-stimulated (35%; P=0.004) lymphocyte serine hydroxymethyltransferase activities in vitro. However, the in vivo fluxes of leucine, methionine, and serine; the rates of homocysteine synthesis and remethylation (total and vitamin B-6-dependent); and the concentrations of homocysteine, methionine, and serine in plasma were not significantly affected by dietary vitamin B-6 restriction.

Conclusions: Moderate vitamin B-6 deficiency does not significantly alter the rates of homocysteine remethylation or synthesis in healthy young adults in the absence of dietary methionine intake.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Carbon Isotopes
  • Deuterium
  • Female
  • Glycine / blood
  • Homocysteine / metabolism*
  • Homocysteine / pharmacokinetics
  • Humans
  • Male
  • Methionine / administration & dosage
  • Methionine / metabolism
  • Methionine / pharmacokinetics
  • Methylation
  • Methylenetetrahydrofolate Reductase (NADPH2) / genetics
  • Polymorphism, Genetic
  • Pyridoxal Phosphate / blood*
  • Serine / administration & dosage
  • Serine / metabolism
  • Serine / pharmacokinetics
  • Vitamin B 6 / administration & dosage
  • Vitamin B 6 / pharmacology*

Substances

  • Carbon Isotopes
  • Homocysteine
  • Serine
  • Pyridoxal Phosphate
  • Vitamin B 6
  • Methionine
  • Deuterium
  • Methylenetetrahydrofolate Reductase (NADPH2)
  • Glycine