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Pharmacokinetic properties of a novel formulation of S-adenosyl-l-methionine phytate

S-adenosyl-l-methionine (SAM), the main endogenous methyl donor, is the adenosyl derivative of the amino acid methionine, which displays many important roles in cellular metabolism. It is widely used as a food supplement and in some countries is also marketed as a drug. Its interesting nutraceutical...

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Autores principales: Francioso, Antonio, Fanelli, Sergio, d’Erme, Maria, Lendaro, Eugenio, Miraglia, Niccolò, Fontana, Mario, Cavallaro, Rosaria A., Mosca, Luciana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Vienna 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8519898/
https://www.ncbi.nlm.nih.gov/pubmed/34536129
http://dx.doi.org/10.1007/s00726-021-03076-7
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author Francioso, Antonio
Fanelli, Sergio
d’Erme, Maria
Lendaro, Eugenio
Miraglia, Niccolò
Fontana, Mario
Cavallaro, Rosaria A.
Mosca, Luciana
author_facet Francioso, Antonio
Fanelli, Sergio
d’Erme, Maria
Lendaro, Eugenio
Miraglia, Niccolò
Fontana, Mario
Cavallaro, Rosaria A.
Mosca, Luciana
author_sort Francioso, Antonio
collection PubMed
description S-adenosyl-l-methionine (SAM), the main endogenous methyl donor, is the adenosyl derivative of the amino acid methionine, which displays many important roles in cellular metabolism. It is widely used as a food supplement and in some countries is also marketed as a drug. Its interesting nutraceutical and pharmacological properties prompted us to evaluate the pharmacokinetics of a new form of SAM, the phytate salt. The product was administered orally to rats and pharmacokinetic parameters were evaluated by comparing the results with that obtained by administering the SAM tosylated form (SAM PTS). It was found that phytate anion protects SAM from degradation, probably because of steric hindrance exerted by the counterion, and that the SAM phytate displayed significant better pharmacokinetic parameters compared to SAM PTS. These results open to the perspective of the use of new salts of SAM endowed with better pharmacokinetic properties.
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spelling pubmed-85198982021-10-29 Pharmacokinetic properties of a novel formulation of S-adenosyl-l-methionine phytate Francioso, Antonio Fanelli, Sergio d’Erme, Maria Lendaro, Eugenio Miraglia, Niccolò Fontana, Mario Cavallaro, Rosaria A. Mosca, Luciana Amino Acids Original Article S-adenosyl-l-methionine (SAM), the main endogenous methyl donor, is the adenosyl derivative of the amino acid methionine, which displays many important roles in cellular metabolism. It is widely used as a food supplement and in some countries is also marketed as a drug. Its interesting nutraceutical and pharmacological properties prompted us to evaluate the pharmacokinetics of a new form of SAM, the phytate salt. The product was administered orally to rats and pharmacokinetic parameters were evaluated by comparing the results with that obtained by administering the SAM tosylated form (SAM PTS). It was found that phytate anion protects SAM from degradation, probably because of steric hindrance exerted by the counterion, and that the SAM phytate displayed significant better pharmacokinetic parameters compared to SAM PTS. These results open to the perspective of the use of new salts of SAM endowed with better pharmacokinetic properties. Springer Vienna 2021-09-18 2021 /pmc/articles/PMC8519898/ /pubmed/34536129 http://dx.doi.org/10.1007/s00726-021-03076-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Francioso, Antonio
Fanelli, Sergio
d’Erme, Maria
Lendaro, Eugenio
Miraglia, Niccolò
Fontana, Mario
Cavallaro, Rosaria A.
Mosca, Luciana
Pharmacokinetic properties of a novel formulation of S-adenosyl-l-methionine phytate
title Pharmacokinetic properties of a novel formulation of S-adenosyl-l-methionine phytate
title_full Pharmacokinetic properties of a novel formulation of S-adenosyl-l-methionine phytate
title_fullStr Pharmacokinetic properties of a novel formulation of S-adenosyl-l-methionine phytate
title_full_unstemmed Pharmacokinetic properties of a novel formulation of S-adenosyl-l-methionine phytate
title_short Pharmacokinetic properties of a novel formulation of S-adenosyl-l-methionine phytate
title_sort pharmacokinetic properties of a novel formulation of s-adenosyl-l-methionine phytate
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8519898/
https://www.ncbi.nlm.nih.gov/pubmed/34536129
http://dx.doi.org/10.1007/s00726-021-03076-7
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