Laura E McBreairty1, Jason L Robinson1, Scott V Harding2, Edward W Randell1,3, Janet A Brunton1, Robert F Bertolo4. 1. Department of Biochemistry, Memorial University of Newfoundland, St. John's, NL, A1B 3X9, Canada. 2. Diabetes and Nutritional Sciences Division, King's College London, London, SE1 9NH, United Kingdom. 3. Faculty of Medicine, Memorial University of Newfoundland, St. John's, NL, A1B 3V6, Canada. 4. Department of Biochemistry, Memorial University of Newfoundland, St. John's, NL, A1B 3X9, Canada. rbertolo@mun.ca.
Abstract
PURPOSE: Both folate and betaine (synthesized from choline) are nutrients used to methylate homocysteine to reform the amino acid methionine following donation of its methyl group; however, it is unclear whether both remethylation pathways are of equal importance during the neonatal period when remethylation rates are high. Methionine is an indispensable amino acid that is in high demand in neonates not only for protein synthesis, but is also particularly important for transmethylation reactions, such as creatine and phosphatidylcholine synthesis. The objective of this study was to determine whether supplementation with folate, betaine, or a combination of both can equally re-synthesize methionine for protein synthesis when dietary methionine is limiting. METHODS: Piglets were fed a low methionine diet devoid of folate, choline, and betaine, and on day 6, piglets were supplemented with either folate, betaine, or folate + betaine (n = 6 per treatment) until day 10. [1-13C]-phenylalanine oxidation was measured as an indicator of methionine availability for protein synthesis both before and after 2 days of supplementation. RESULTS: Prior to supplementation, piglets had lower concentrations of plasma folate, betaine, and choline compared to baseline with no change in homocysteine. Post-supplementation, phenylalanine oxidation levels were 20-46 % lower with any methyl donor supplementation (P = 0.006) with no difference among different supplementation groups. Furthermore, both methyl donors led to similarly lower concentrations of homocysteine following supplementation (P < 0.05). CONCLUSIONS: These data demonstrate an equal capacity for betaine and folate to remethylate methionine for protein synthesis, as indicated by lower phenylalanine oxidation.
PURPOSE: Both folate and betaine (synthesized from choline) are nutrients used to methylate homocysteine to reform the amino acid methionine following donation of its methyl group; however, it is unclear whether both remethylation pathways are of equal importance during the neonatal period when remethylation rates are high. Methionine is an indispensable amino acid that is in high demand in neonates not only for protein synthesis, but is also particularly important for transmethylation reactions, such as creatine and phosphatidylcholine synthesis. The objective of this study was to determine whether supplementation with folate, betaine, or a combination of both can equally re-synthesize methionine for protein synthesis when dietary methionine is limiting. METHODS: Piglets were fed a low methionine diet devoid of folate, choline, and betaine, and on day 6, piglets were supplemented with either folate, betaine, or folate + betaine (n = 6 per treatment) until day 10. [1-13C]-phenylalanine oxidation was measured as an indicator of methionine availability for protein synthesis both before and after 2 days of supplementation. RESULTS: Prior to supplementation, piglets had lower concentrations of plasma folate, betaine, and choline compared to baseline with no change in homocysteine. Post-supplementation, phenylalanine oxidation levels were 20-46 % lower with any methyl donor supplementation (P = 0.006) with no difference among different supplementation groups. Furthermore, both methyl donors led to similarly lower concentrations of homocysteine following supplementation (P < 0.05). CONCLUSIONS: These data demonstrate an equal capacity for betaine and folate to remethylate methionine for protein synthesis, as indicated by lower phenylalanine oxidation.
Entities:
Keywords:
1-Carbon metabolism; Betaine; Folate; Piglet; Protein synthesis
Authors: Leslie M Fischer; Kerry Ann da Costa; Joseph Galanko; Wei Sha; Brigitte Stephenson; Julie Vick; Steven H Zeisel Journal: Am J Clin Nutr Date: 2010-06-09 Impact factor: 7.045
Authors: Steven R Davis; Peter W Stacpoole; Jerry Williamson; Lilia S Kick; Eoin P Quinlivan; Bonnie S Coats; Barry Shane; Lynn B Bailey; Jesse F Gregory Journal: Am J Physiol Endocrinol Metab Date: 2003-10-14 Impact factor: 4.310
Authors: John T Brosnan; Enoka P Wijekoon; Lori Warford-Woolgar; Nathalie L Trottier; Margaret E Brosnan; Janet A Brunton; Robert F P Bertolo Journal: J Nutr Date: 2009-05-27 Impact factor: 4.798