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Role of Intestinal Microbiota in Metabolism of Voglibose In Vitro and In Vivo

BACKGROUND: Voglibose, an α-glucosidase inhibitor, inhibits breakdown of complex carbohydrates into simple sugar units in intestine. Studies showed that voglibose metabolism in the liver might be negligible due to its poor intestinal absorption. Numerous microorganisms live in intestine and have sev...

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Autores principales: Nepal, Mahesh Raj, Kang, Mi Jeong, Kim, Geon Ho, Cha, Dong Ho, Kim, Ju-Hyun, Jeong, Tae Cheon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Diabetes Association 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7801763/
https://www.ncbi.nlm.nih.gov/pubmed/32431100
http://dx.doi.org/10.4093/dmj.2019.0147
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author Nepal, Mahesh Raj
Kang, Mi Jeong
Kim, Geon Ho
Cha, Dong Ho
Kim, Ju-Hyun
Jeong, Tae Cheon
author_facet Nepal, Mahesh Raj
Kang, Mi Jeong
Kim, Geon Ho
Cha, Dong Ho
Kim, Ju-Hyun
Jeong, Tae Cheon
author_sort Nepal, Mahesh Raj
collection PubMed
description BACKGROUND: Voglibose, an α-glucosidase inhibitor, inhibits breakdown of complex carbohydrates into simple sugar units in intestine. Studies showed that voglibose metabolism in the liver might be negligible due to its poor intestinal absorption. Numerous microorganisms live in intestine and have several roles in metabolism and detoxification of various xenobiotics. Due to the limited information, the possible metabolism of voglibose by intestinal microbiota was investigated in vitro and in vivo. METHODS: For the in vitro study, different concentrations of voglibose were incubated with intestinal contents, prepared from both vehicle- and antibiotics-treated mice, to determine the decreased amount of voglibose over time by using liquid chromatography-mass spectrometry. Similarly, in vivo pharmacodynamic effect of voglibose was determined following the administration of voglibose and starch in vehicle- and antibiotic-pretreated non-diabetic and diabetic mice, by measuring the modulatory effects of voglibose on blood glucose levels. RESULTS: The in vitro results indicated that the remaining voglibose could be significantly decreased when incubated with the intestinal contents from normal mice compared to those from antibiotic-treated mice, which had less enzyme activities. The in vivo results showed that the antibiotic pretreatment resulted in reduced metabolism of voglibose. This significantly lowered blood glucose levels in antibiotic-pretreated mice compared to the control animals. CONCLUSION: The present results indicate that voglibose would be metabolized by the intestinal microbiota, and that this metabolism might be pharmacodynamically critical in lowering blood glucose levels in mice.
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spelling pubmed-78017632021-01-22 Role of Intestinal Microbiota in Metabolism of Voglibose In Vitro and In Vivo Nepal, Mahesh Raj Kang, Mi Jeong Kim, Geon Ho Cha, Dong Ho Kim, Ju-Hyun Jeong, Tae Cheon Diabetes Metab J Original Article BACKGROUND: Voglibose, an α-glucosidase inhibitor, inhibits breakdown of complex carbohydrates into simple sugar units in intestine. Studies showed that voglibose metabolism in the liver might be negligible due to its poor intestinal absorption. Numerous microorganisms live in intestine and have several roles in metabolism and detoxification of various xenobiotics. Due to the limited information, the possible metabolism of voglibose by intestinal microbiota was investigated in vitro and in vivo. METHODS: For the in vitro study, different concentrations of voglibose were incubated with intestinal contents, prepared from both vehicle- and antibiotics-treated mice, to determine the decreased amount of voglibose over time by using liquid chromatography-mass spectrometry. Similarly, in vivo pharmacodynamic effect of voglibose was determined following the administration of voglibose and starch in vehicle- and antibiotic-pretreated non-diabetic and diabetic mice, by measuring the modulatory effects of voglibose on blood glucose levels. RESULTS: The in vitro results indicated that the remaining voglibose could be significantly decreased when incubated with the intestinal contents from normal mice compared to those from antibiotic-treated mice, which had less enzyme activities. The in vivo results showed that the antibiotic pretreatment resulted in reduced metabolism of voglibose. This significantly lowered blood glucose levels in antibiotic-pretreated mice compared to the control animals. CONCLUSION: The present results indicate that voglibose would be metabolized by the intestinal microbiota, and that this metabolism might be pharmacodynamically critical in lowering blood glucose levels in mice. Korean Diabetes Association 2020-12 2020-04-06 /pmc/articles/PMC7801763/ /pubmed/32431100 http://dx.doi.org/10.4093/dmj.2019.0147 Text en Copyright © 2020 Korean Diabetes Association https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Nepal, Mahesh Raj
Kang, Mi Jeong
Kim, Geon Ho
Cha, Dong Ho
Kim, Ju-Hyun
Jeong, Tae Cheon
Role of Intestinal Microbiota in Metabolism of Voglibose In Vitro and In Vivo
title Role of Intestinal Microbiota in Metabolism of Voglibose In Vitro and In Vivo
title_full Role of Intestinal Microbiota in Metabolism of Voglibose In Vitro and In Vivo
title_fullStr Role of Intestinal Microbiota in Metabolism of Voglibose In Vitro and In Vivo
title_full_unstemmed Role of Intestinal Microbiota in Metabolism of Voglibose In Vitro and In Vivo
title_short Role of Intestinal Microbiota in Metabolism of Voglibose In Vitro and In Vivo
title_sort role of intestinal microbiota in metabolism of voglibose in vitro and in vivo
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7801763/
https://www.ncbi.nlm.nih.gov/pubmed/32431100
http://dx.doi.org/10.4093/dmj.2019.0147
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