Cargando…

Short‐term exposure to synthetic flaxseed lignan LGM2605 alters gut microbiota in mice

LGM2605 is a synthetic version of the naturally occurring flaxseed lignan secoisolariciresinol diglucoside (SDG), with known anti‐inflammatory and antioxidant properties; however, its effects on gut microbial composition have not previously been evaluated. In the present study, we sought to determin...

Descripción completa

Detalles Bibliográficos
Autores principales: Badger, Reagan, Aho, Ken, Serve, Kinta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8087944/
https://www.ncbi.nlm.nih.gov/pubmed/33970540
http://dx.doi.org/10.1002/mbo3.1185
_version_ 1783686758192381952
author Badger, Reagan
Aho, Ken
Serve, Kinta
author_facet Badger, Reagan
Aho, Ken
Serve, Kinta
author_sort Badger, Reagan
collection PubMed
description LGM2605 is a synthetic version of the naturally occurring flaxseed lignan secoisolariciresinol diglucoside (SDG), with known anti‐inflammatory and antioxidant properties; however, its effects on gut microbial composition have not previously been evaluated. In the present study, we sought to determine how the 10‐day oral administration of LGM2605 alters the gut microbiota of mice. Eight‐week‐old female C57BL/6 mice were treated with either LGM2605 or saline, administered daily via oral gavage over a 10‐day treatment period. Upon termination of treatment, mouse cecums (n = 31) were collected, and cecal DNA was isolated. 16S rRNA genes were sequenced and analyzed in Mothur to identify changes in gut microbial composition induced by LGM2605 treatment (v. saline control). We then assessed community composition, performed indicator taxa analysis, and measured alpha and beta diversity. Overall, LGM2605 significantly altered the gut microbiota of mice; we reported alterations in 3 bacterial phyla and 22 genera as a result of treatment. The study here identifies for the first time significant alterations in the gut microbiota of mice following oral administration of LGM2605, in general shifting toward a more anti‐inflammatory composition. These findings lay the foundation for future investigations utilizing LGM2605 to control gut dysbiosis and, by extension, systemic inflammation.
format Online
Article
Text
id pubmed-8087944
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-80879442021-05-07 Short‐term exposure to synthetic flaxseed lignan LGM2605 alters gut microbiota in mice Badger, Reagan Aho, Ken Serve, Kinta Microbiologyopen Original Articles LGM2605 is a synthetic version of the naturally occurring flaxseed lignan secoisolariciresinol diglucoside (SDG), with known anti‐inflammatory and antioxidant properties; however, its effects on gut microbial composition have not previously been evaluated. In the present study, we sought to determine how the 10‐day oral administration of LGM2605 alters the gut microbiota of mice. Eight‐week‐old female C57BL/6 mice were treated with either LGM2605 or saline, administered daily via oral gavage over a 10‐day treatment period. Upon termination of treatment, mouse cecums (n = 31) were collected, and cecal DNA was isolated. 16S rRNA genes were sequenced and analyzed in Mothur to identify changes in gut microbial composition induced by LGM2605 treatment (v. saline control). We then assessed community composition, performed indicator taxa analysis, and measured alpha and beta diversity. Overall, LGM2605 significantly altered the gut microbiota of mice; we reported alterations in 3 bacterial phyla and 22 genera as a result of treatment. The study here identifies for the first time significant alterations in the gut microbiota of mice following oral administration of LGM2605, in general shifting toward a more anti‐inflammatory composition. These findings lay the foundation for future investigations utilizing LGM2605 to control gut dysbiosis and, by extension, systemic inflammation. John Wiley and Sons Inc. 2021-05-01 /pmc/articles/PMC8087944/ /pubmed/33970540 http://dx.doi.org/10.1002/mbo3.1185 Text en © 2021 The Authors. MicrobiologyOpen published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Badger, Reagan
Aho, Ken
Serve, Kinta
Short‐term exposure to synthetic flaxseed lignan LGM2605 alters gut microbiota in mice
title Short‐term exposure to synthetic flaxseed lignan LGM2605 alters gut microbiota in mice
title_full Short‐term exposure to synthetic flaxseed lignan LGM2605 alters gut microbiota in mice
title_fullStr Short‐term exposure to synthetic flaxseed lignan LGM2605 alters gut microbiota in mice
title_full_unstemmed Short‐term exposure to synthetic flaxseed lignan LGM2605 alters gut microbiota in mice
title_short Short‐term exposure to synthetic flaxseed lignan LGM2605 alters gut microbiota in mice
title_sort short‐term exposure to synthetic flaxseed lignan lgm2605 alters gut microbiota in mice
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8087944/
https://www.ncbi.nlm.nih.gov/pubmed/33970540
http://dx.doi.org/10.1002/mbo3.1185
work_keys_str_mv AT badgerreagan shorttermexposuretosyntheticflaxseedlignanlgm2605altersgutmicrobiotainmice
AT ahoken shorttermexposuretosyntheticflaxseedlignanlgm2605altersgutmicrobiotainmice
AT servekinta shorttermexposuretosyntheticflaxseedlignanlgm2605altersgutmicrobiotainmice