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Subchronic Tolerance Trials of Graded Oral Supplementation with Phenylalanine or Serine in Healthy Adults

Phenylalanine and serine are amino acids used in dietary supplements and nutritional products consumed by healthy consumers; however, the safe level of phenylalanine or serine supplementation is unknown. The objective of this study was to conduct two 4-week clinical trials to evaluate the safety and...

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Autores principales: Miura, Naoki, Matsumoto, Hideki, Cynober, Luc, Stover, Patrick J., Elango, Rajavel, Kadowaki, Motoni, Bier, Dennis M., Smriga, Miro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8227932/
https://www.ncbi.nlm.nih.gov/pubmed/34201370
http://dx.doi.org/10.3390/nu13061976
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author Miura, Naoki
Matsumoto, Hideki
Cynober, Luc
Stover, Patrick J.
Elango, Rajavel
Kadowaki, Motoni
Bier, Dennis M.
Smriga, Miro
author_facet Miura, Naoki
Matsumoto, Hideki
Cynober, Luc
Stover, Patrick J.
Elango, Rajavel
Kadowaki, Motoni
Bier, Dennis M.
Smriga, Miro
author_sort Miura, Naoki
collection PubMed
description Phenylalanine and serine are amino acids used in dietary supplements and nutritional products consumed by healthy consumers; however, the safe level of phenylalanine or serine supplementation is unknown. The objective of this study was to conduct two 4-week clinical trials to evaluate the safety and tolerability of graded dosages of oral phenylalanine and oral serine. Healthy male adults (n = 60, 38.2 ± 1.8y) completed graded dosages of either phenylalanine or serine supplement (3, 6, 9 and 12 g/d) for 4 weeks with 2-week wash-out periods in between. Primary outcomes included vitals, a broad spectrum of circulating biochemical analytes, body weight, sleep quality and mental self-assessment. At low dosages, minor changes in serum electrolytes and plasma non-essential amino acids glutamine and aspartic acid concentrations were observed. Serine increased its plasma concentrations at high supplemental dosages (9 and 12 g/day), and phenylalanine increased plasma tyrosine concentrations at 12 g/day, but those changes were not considered toxicologically relevant. No other changes in measured parameters were observed, and study subjects tolerated 4-week-long oral supplementation of phenylalanine or serine without treatment-related adverse events. A clinical, no-observed-adverse-effect-level (NOAEL) of phenylalanine and serine supplementation in healthy adult males was determined to be 12 g/day.
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spelling pubmed-82279322021-06-26 Subchronic Tolerance Trials of Graded Oral Supplementation with Phenylalanine or Serine in Healthy Adults Miura, Naoki Matsumoto, Hideki Cynober, Luc Stover, Patrick J. Elango, Rajavel Kadowaki, Motoni Bier, Dennis M. Smriga, Miro Nutrients Article Phenylalanine and serine are amino acids used in dietary supplements and nutritional products consumed by healthy consumers; however, the safe level of phenylalanine or serine supplementation is unknown. The objective of this study was to conduct two 4-week clinical trials to evaluate the safety and tolerability of graded dosages of oral phenylalanine and oral serine. Healthy male adults (n = 60, 38.2 ± 1.8y) completed graded dosages of either phenylalanine or serine supplement (3, 6, 9 and 12 g/d) for 4 weeks with 2-week wash-out periods in between. Primary outcomes included vitals, a broad spectrum of circulating biochemical analytes, body weight, sleep quality and mental self-assessment. At low dosages, minor changes in serum electrolytes and plasma non-essential amino acids glutamine and aspartic acid concentrations were observed. Serine increased its plasma concentrations at high supplemental dosages (9 and 12 g/day), and phenylalanine increased plasma tyrosine concentrations at 12 g/day, but those changes were not considered toxicologically relevant. No other changes in measured parameters were observed, and study subjects tolerated 4-week-long oral supplementation of phenylalanine or serine without treatment-related adverse events. A clinical, no-observed-adverse-effect-level (NOAEL) of phenylalanine and serine supplementation in healthy adult males was determined to be 12 g/day. MDPI 2021-06-08 /pmc/articles/PMC8227932/ /pubmed/34201370 http://dx.doi.org/10.3390/nu13061976 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Miura, Naoki
Matsumoto, Hideki
Cynober, Luc
Stover, Patrick J.
Elango, Rajavel
Kadowaki, Motoni
Bier, Dennis M.
Smriga, Miro
Subchronic Tolerance Trials of Graded Oral Supplementation with Phenylalanine or Serine in Healthy Adults
title Subchronic Tolerance Trials of Graded Oral Supplementation with Phenylalanine or Serine in Healthy Adults
title_full Subchronic Tolerance Trials of Graded Oral Supplementation with Phenylalanine or Serine in Healthy Adults
title_fullStr Subchronic Tolerance Trials of Graded Oral Supplementation with Phenylalanine or Serine in Healthy Adults
title_full_unstemmed Subchronic Tolerance Trials of Graded Oral Supplementation with Phenylalanine or Serine in Healthy Adults
title_short Subchronic Tolerance Trials of Graded Oral Supplementation with Phenylalanine or Serine in Healthy Adults
title_sort subchronic tolerance trials of graded oral supplementation with phenylalanine or serine in healthy adults
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8227932/
https://www.ncbi.nlm.nih.gov/pubmed/34201370
http://dx.doi.org/10.3390/nu13061976
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