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Effect of a Bifidobacterium-Containing Acid-Resistant Microcapsule Formulation on Gut Microbiota: A Pilot Study

Approximately 10 Bifidobacterium species are known to inhabit the human intestinal tract. Bifidobacteria have been reported to possess a variety of probiotic benefits. However, when bifidobacteria are consumed internally as probiotics, the bacteria are killed by gastric acid. Therefore, we developed...

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Autores principales: Minami, Miki, Tsuji, Shoji, Akagawa, Shohei, Akagawa, Yuko, Yoshimoto, Yuki, Kawakami, Hirosato, Kohno, Mamiko, Kaneko, Kazunari
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9693766/
https://www.ncbi.nlm.nih.gov/pubmed/36432516
http://dx.doi.org/10.3390/nu14224829
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author Minami, Miki
Tsuji, Shoji
Akagawa, Shohei
Akagawa, Yuko
Yoshimoto, Yuki
Kawakami, Hirosato
Kohno, Mamiko
Kaneko, Kazunari
author_facet Minami, Miki
Tsuji, Shoji
Akagawa, Shohei
Akagawa, Yuko
Yoshimoto, Yuki
Kawakami, Hirosato
Kohno, Mamiko
Kaneko, Kazunari
author_sort Minami, Miki
collection PubMed
description Approximately 10 Bifidobacterium species are known to inhabit the human intestinal tract. Bifidobacteria have been reported to possess a variety of probiotic benefits. However, when bifidobacteria are consumed internally as probiotics, the bacteria are killed by gastric acid. Therefore, we developed acid-resistant microcapsules containing Bifidobacterium breve M-16V and B. longum BB536, which are unaffected by gastric acid, and evaluated whether the microcapsule formulation increased the amount of bifidobacteria in the stool after administration compared with the powder formulation. The results revealed no significant difference in the percentage or number of B. longum between before and after administration of the powder or microcapsule formulation in children. By contrast, the bacterial count of B. breve was significantly increased after microcapsule formulation administration (1.5 × 10(5) copies/g after administration versus 2.8 × 10(4) copies/g before administration, p = 0.013). In addition, the increase in the bacterial count of B. breve in stools after administration of microcapsule formulation was approximately 1000-fold higher than that after powder formulation administration (p = 0.018). In conclusion, the results indicate that the microcapsule formulation is efficiently transferred to the large intestine without the adverse effects of gastric acidity in children.
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spelling pubmed-96937662022-11-26 Effect of a Bifidobacterium-Containing Acid-Resistant Microcapsule Formulation on Gut Microbiota: A Pilot Study Minami, Miki Tsuji, Shoji Akagawa, Shohei Akagawa, Yuko Yoshimoto, Yuki Kawakami, Hirosato Kohno, Mamiko Kaneko, Kazunari Nutrients Article Approximately 10 Bifidobacterium species are known to inhabit the human intestinal tract. Bifidobacteria have been reported to possess a variety of probiotic benefits. However, when bifidobacteria are consumed internally as probiotics, the bacteria are killed by gastric acid. Therefore, we developed acid-resistant microcapsules containing Bifidobacterium breve M-16V and B. longum BB536, which are unaffected by gastric acid, and evaluated whether the microcapsule formulation increased the amount of bifidobacteria in the stool after administration compared with the powder formulation. The results revealed no significant difference in the percentage or number of B. longum between before and after administration of the powder or microcapsule formulation in children. By contrast, the bacterial count of B. breve was significantly increased after microcapsule formulation administration (1.5 × 10(5) copies/g after administration versus 2.8 × 10(4) copies/g before administration, p = 0.013). In addition, the increase in the bacterial count of B. breve in stools after administration of microcapsule formulation was approximately 1000-fold higher than that after powder formulation administration (p = 0.018). In conclusion, the results indicate that the microcapsule formulation is efficiently transferred to the large intestine without the adverse effects of gastric acidity in children. MDPI 2022-11-15 /pmc/articles/PMC9693766/ /pubmed/36432516 http://dx.doi.org/10.3390/nu14224829 Text en © 2022 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
Minami, Miki
Tsuji, Shoji
Akagawa, Shohei
Akagawa, Yuko
Yoshimoto, Yuki
Kawakami, Hirosato
Kohno, Mamiko
Kaneko, Kazunari
Effect of a Bifidobacterium-Containing Acid-Resistant Microcapsule Formulation on Gut Microbiota: A Pilot Study
title Effect of a Bifidobacterium-Containing Acid-Resistant Microcapsule Formulation on Gut Microbiota: A Pilot Study
title_full Effect of a Bifidobacterium-Containing Acid-Resistant Microcapsule Formulation on Gut Microbiota: A Pilot Study
title_fullStr Effect of a Bifidobacterium-Containing Acid-Resistant Microcapsule Formulation on Gut Microbiota: A Pilot Study
title_full_unstemmed Effect of a Bifidobacterium-Containing Acid-Resistant Microcapsule Formulation on Gut Microbiota: A Pilot Study
title_short Effect of a Bifidobacterium-Containing Acid-Resistant Microcapsule Formulation on Gut Microbiota: A Pilot Study
title_sort effect of a bifidobacterium-containing acid-resistant microcapsule formulation on gut microbiota: a pilot study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9693766/
https://www.ncbi.nlm.nih.gov/pubmed/36432516
http://dx.doi.org/10.3390/nu14224829
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