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A randomized trial to evaluate the impact of copra meal hydrolysate on gastrointestinal symptoms and gut microbiome
The impact of copra meal hydrolysate (CMH) on gut health was assessed by conducting a double-blinded, placebo-controlled study. Sixty healthy adult participants, aged 18–40 years were assigned to daily consume 3 g of CMH, 5 g of CMH or placebo in the form of drink powder for 21 days. Consumption of...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PeerJ Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8449532/ https://www.ncbi.nlm.nih.gov/pubmed/34616618 http://dx.doi.org/10.7717/peerj.12158 |
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author | Sathitkowitchai, Witida Suratannon, Narissara Keawsompong, Suttipun Weerapakorn, Wanlapa Patumcharoenpol, Preecha Nitisinprasert, Sunee Nakphaichit, Massalin |
author_facet | Sathitkowitchai, Witida Suratannon, Narissara Keawsompong, Suttipun Weerapakorn, Wanlapa Patumcharoenpol, Preecha Nitisinprasert, Sunee Nakphaichit, Massalin |
author_sort | Sathitkowitchai, Witida |
collection | PubMed |
description | The impact of copra meal hydrolysate (CMH) on gut health was assessed by conducting a double-blinded, placebo-controlled study. Sixty healthy adult participants, aged 18–40 years were assigned to daily consume 3 g of CMH, 5 g of CMH or placebo in the form of drink powder for 21 days. Consumption of CMH at 3 g/d improved defecating conditions by reducing stool size and also relieved flatulence and bloating symptoms. Fecal samples were collected serially at the baseline before treatment, after the treatment and after a 2-week washout period. The gut microbiomes were similar among the treatment groups, with microbial community changes observed within the groups. Intake of CMH at 3 g/d led to increase microbial diversity and richness. Reduction of the ratio between Firmicutes to Bacteroidetes was observed, although it was not significantly different between the groups. The 3 g/d CMH treatment increased beneficial microbes in the group of fiber-degrading bacteria, especially human colonic Bacteroidetes, while induction of Bifidobacteriaceae was observed after the washout period. Intake of CMH led to increase lactic acid production, while 3 g/d supplement promoted the present of immunoglobulin A (IgA) in stool samples. The 3 g daily dose of CMH led to the potentially beneficial effects on gut health for healthy individuals. |
format | Online Article Text |
id | pubmed-8449532 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | PeerJ Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84495322021-10-05 A randomized trial to evaluate the impact of copra meal hydrolysate on gastrointestinal symptoms and gut microbiome Sathitkowitchai, Witida Suratannon, Narissara Keawsompong, Suttipun Weerapakorn, Wanlapa Patumcharoenpol, Preecha Nitisinprasert, Sunee Nakphaichit, Massalin PeerJ Microbiology The impact of copra meal hydrolysate (CMH) on gut health was assessed by conducting a double-blinded, placebo-controlled study. Sixty healthy adult participants, aged 18–40 years were assigned to daily consume 3 g of CMH, 5 g of CMH or placebo in the form of drink powder for 21 days. Consumption of CMH at 3 g/d improved defecating conditions by reducing stool size and also relieved flatulence and bloating symptoms. Fecal samples were collected serially at the baseline before treatment, after the treatment and after a 2-week washout period. The gut microbiomes were similar among the treatment groups, with microbial community changes observed within the groups. Intake of CMH at 3 g/d led to increase microbial diversity and richness. Reduction of the ratio between Firmicutes to Bacteroidetes was observed, although it was not significantly different between the groups. The 3 g/d CMH treatment increased beneficial microbes in the group of fiber-degrading bacteria, especially human colonic Bacteroidetes, while induction of Bifidobacteriaceae was observed after the washout period. Intake of CMH led to increase lactic acid production, while 3 g/d supplement promoted the present of immunoglobulin A (IgA) in stool samples. The 3 g daily dose of CMH led to the potentially beneficial effects on gut health for healthy individuals. PeerJ Inc. 2021-09-15 /pmc/articles/PMC8449532/ /pubmed/34616618 http://dx.doi.org/10.7717/peerj.12158 Text en ©2021 Sathitkowitchai et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited. |
spellingShingle | Microbiology Sathitkowitchai, Witida Suratannon, Narissara Keawsompong, Suttipun Weerapakorn, Wanlapa Patumcharoenpol, Preecha Nitisinprasert, Sunee Nakphaichit, Massalin A randomized trial to evaluate the impact of copra meal hydrolysate on gastrointestinal symptoms and gut microbiome |
title | A randomized trial to evaluate the impact of copra meal hydrolysate on gastrointestinal symptoms and gut microbiome |
title_full | A randomized trial to evaluate the impact of copra meal hydrolysate on gastrointestinal symptoms and gut microbiome |
title_fullStr | A randomized trial to evaluate the impact of copra meal hydrolysate on gastrointestinal symptoms and gut microbiome |
title_full_unstemmed | A randomized trial to evaluate the impact of copra meal hydrolysate on gastrointestinal symptoms and gut microbiome |
title_short | A randomized trial to evaluate the impact of copra meal hydrolysate on gastrointestinal symptoms and gut microbiome |
title_sort | randomized trial to evaluate the impact of copra meal hydrolysate on gastrointestinal symptoms and gut microbiome |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8449532/ https://www.ncbi.nlm.nih.gov/pubmed/34616618 http://dx.doi.org/10.7717/peerj.12158 |
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