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Acute effects of the food preservative propionic acid on glucose metabolism in humans
INTRODUCTION: Propionic acid (PA) is a common food preservative generally recognized as safe by the US Food and Drug Administration; however, exogenous PA has effects on glucose metabolism that are not fully understood. Our preclinical studies demonstrated exogenous PA increases glucagon, norepineph...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BMJ Publishing Group
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8314753/ https://www.ncbi.nlm.nih.gov/pubmed/34312159 http://dx.doi.org/10.1136/bmjdrc-2021-002336 |
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author | Adler, Gail K Hornik, Ezra S Murray, Gillian Bhandari, Shreya Yadav, Yogesh Heydarpour, Mahyar Basu, Rita Garg, Rajesh Tirosh, Amir |
author_facet | Adler, Gail K Hornik, Ezra S Murray, Gillian Bhandari, Shreya Yadav, Yogesh Heydarpour, Mahyar Basu, Rita Garg, Rajesh Tirosh, Amir |
author_sort | Adler, Gail K |
collection | PubMed |
description | INTRODUCTION: Propionic acid (PA) is a common food preservative generally recognized as safe by the US Food and Drug Administration; however, exogenous PA has effects on glucose metabolism that are not fully understood. Our preclinical studies demonstrated exogenous PA increases glucagon, norepinephrine, and endogenous glucose production (EGP). RESEARCH DESIGN AND METHODS: We performed a randomized, placebo-controlled, crossover study in 28 healthy men and women to determine the effect of PA (1500 mg calcium propionate) on these factors. Subjects had two study visits, each preceded by a 1 week, PA-free diet. During each visit, glucose, insulin, glucagon, norepinephrine, epinephrine, and EGP were assessed for 2 hours after oral administration of PA/placebo under resting conditions (protocol 1) and during either a euglycemic (~85–90 mg/dL) or hypoglycemic (~65–70 mg/dL) hyperinsulinemic clamp (protocol 2). RESULTS: PA, as compared with placebo, significantly increased: (1) glucagon and norepinephrine during protocol 1; (2) glucagon, norepinephrine, and epinephrine under euglycemic conditions in protocol 2; and (3) norepinephrine, epinephrine, and EGP under hypoglycemic conditions in protocol 2. CONCLUSION: Oral consumption of PA leads to inappropriate activation of the insulin counterregulatory hormonal network. This inappropriate stimulation highlights PA as a potential metabolic disruptor. |
format | Online Article Text |
id | pubmed-8314753 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-83147532021-08-13 Acute effects of the food preservative propionic acid on glucose metabolism in humans Adler, Gail K Hornik, Ezra S Murray, Gillian Bhandari, Shreya Yadav, Yogesh Heydarpour, Mahyar Basu, Rita Garg, Rajesh Tirosh, Amir BMJ Open Diabetes Res Care Metabolism INTRODUCTION: Propionic acid (PA) is a common food preservative generally recognized as safe by the US Food and Drug Administration; however, exogenous PA has effects on glucose metabolism that are not fully understood. Our preclinical studies demonstrated exogenous PA increases glucagon, norepinephrine, and endogenous glucose production (EGP). RESEARCH DESIGN AND METHODS: We performed a randomized, placebo-controlled, crossover study in 28 healthy men and women to determine the effect of PA (1500 mg calcium propionate) on these factors. Subjects had two study visits, each preceded by a 1 week, PA-free diet. During each visit, glucose, insulin, glucagon, norepinephrine, epinephrine, and EGP were assessed for 2 hours after oral administration of PA/placebo under resting conditions (protocol 1) and during either a euglycemic (~85–90 mg/dL) or hypoglycemic (~65–70 mg/dL) hyperinsulinemic clamp (protocol 2). RESULTS: PA, as compared with placebo, significantly increased: (1) glucagon and norepinephrine during protocol 1; (2) glucagon, norepinephrine, and epinephrine under euglycemic conditions in protocol 2; and (3) norepinephrine, epinephrine, and EGP under hypoglycemic conditions in protocol 2. CONCLUSION: Oral consumption of PA leads to inappropriate activation of the insulin counterregulatory hormonal network. This inappropriate stimulation highlights PA as a potential metabolic disruptor. BMJ Publishing Group 2021-07-26 /pmc/articles/PMC8314753/ /pubmed/34312159 http://dx.doi.org/10.1136/bmjdrc-2021-002336 Text en © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Metabolism Adler, Gail K Hornik, Ezra S Murray, Gillian Bhandari, Shreya Yadav, Yogesh Heydarpour, Mahyar Basu, Rita Garg, Rajesh Tirosh, Amir Acute effects of the food preservative propionic acid on glucose metabolism in humans |
title | Acute effects of the food preservative propionic acid on glucose metabolism in humans |
title_full | Acute effects of the food preservative propionic acid on glucose metabolism in humans |
title_fullStr | Acute effects of the food preservative propionic acid on glucose metabolism in humans |
title_full_unstemmed | Acute effects of the food preservative propionic acid on glucose metabolism in humans |
title_short | Acute effects of the food preservative propionic acid on glucose metabolism in humans |
title_sort | acute effects of the food preservative propionic acid on glucose metabolism in humans |
topic | Metabolism |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8314753/ https://www.ncbi.nlm.nih.gov/pubmed/34312159 http://dx.doi.org/10.1136/bmjdrc-2021-002336 |
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