Cargando…

Upregulation of colonic luminal polyamines produced by intestinal microbiota delays senescence in mice

Prevention of quality of life (QOL) deterioration is associated with the inhibition of geriatric diseases and the regulation of brain function. However, no substance is known that prevents the aging of both body and brain. It is known that polyamine concentrations in somatic tissues (including the b...

Descripción completa

Detalles Bibliográficos
Autores principales: Kibe, Ryoko, Kurihara, Shin, Sakai, Yumi, Suzuki, Hideyuki, Ooga, Takushi, Sawaki, Emiko, Muramatsu, Koji, Nakamura, Atsuo, Yamashita, Ayano, Kitada, Yusuke, Kakeyama, Masaki, Benno, Yoshimi, Matsumoto, Mitsuharu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4070089/
https://www.ncbi.nlm.nih.gov/pubmed/24686447
http://dx.doi.org/10.1038/srep04548
_version_ 1782322639625256960
author Kibe, Ryoko
Kurihara, Shin
Sakai, Yumi
Suzuki, Hideyuki
Ooga, Takushi
Sawaki, Emiko
Muramatsu, Koji
Nakamura, Atsuo
Yamashita, Ayano
Kitada, Yusuke
Kakeyama, Masaki
Benno, Yoshimi
Matsumoto, Mitsuharu
author_facet Kibe, Ryoko
Kurihara, Shin
Sakai, Yumi
Suzuki, Hideyuki
Ooga, Takushi
Sawaki, Emiko
Muramatsu, Koji
Nakamura, Atsuo
Yamashita, Ayano
Kitada, Yusuke
Kakeyama, Masaki
Benno, Yoshimi
Matsumoto, Mitsuharu
author_sort Kibe, Ryoko
collection PubMed
description Prevention of quality of life (QOL) deterioration is associated with the inhibition of geriatric diseases and the regulation of brain function. However, no substance is known that prevents the aging of both body and brain. It is known that polyamine concentrations in somatic tissues (including the brain) decrease with increasing age, and polyamine-rich foods enhance longevity in yeast, worms, flies, and mice, and protect flies from age-induced memory impairment. A main source of exogenous polyamines is the intestinal lumen, where they are produced by intestinal bacteria. We found that arginine intake increased the concentration of putrescine in the colon and increased levels of spermidine and spermine in the blood. Mice orally administered with arginine in combination with the probiotic bifidobacteria LKM512 long-term showed suppressed inflammation, improved longevity, and protection from age-induced memory impairment. This study shows that intake of arginine and LKM512 may prevent aging-dependent declines in QOL via the upregulation of polyamines.
format Online
Article
Text
id pubmed-4070089
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-40700892014-08-27 Upregulation of colonic luminal polyamines produced by intestinal microbiota delays senescence in mice Kibe, Ryoko Kurihara, Shin Sakai, Yumi Suzuki, Hideyuki Ooga, Takushi Sawaki, Emiko Muramatsu, Koji Nakamura, Atsuo Yamashita, Ayano Kitada, Yusuke Kakeyama, Masaki Benno, Yoshimi Matsumoto, Mitsuharu Sci Rep Article Prevention of quality of life (QOL) deterioration is associated with the inhibition of geriatric diseases and the regulation of brain function. However, no substance is known that prevents the aging of both body and brain. It is known that polyamine concentrations in somatic tissues (including the brain) decrease with increasing age, and polyamine-rich foods enhance longevity in yeast, worms, flies, and mice, and protect flies from age-induced memory impairment. A main source of exogenous polyamines is the intestinal lumen, where they are produced by intestinal bacteria. We found that arginine intake increased the concentration of putrescine in the colon and increased levels of spermidine and spermine in the blood. Mice orally administered with arginine in combination with the probiotic bifidobacteria LKM512 long-term showed suppressed inflammation, improved longevity, and protection from age-induced memory impairment. This study shows that intake of arginine and LKM512 may prevent aging-dependent declines in QOL via the upregulation of polyamines. Nature Publishing Group 2014-04-01 /pmc/articles/PMC4070089/ /pubmed/24686447 http://dx.doi.org/10.1038/srep04548 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. The images in this article are included in the article's Creative Commons license, unless indicated otherwise in the image credit; if the image is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the image. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Article
Kibe, Ryoko
Kurihara, Shin
Sakai, Yumi
Suzuki, Hideyuki
Ooga, Takushi
Sawaki, Emiko
Muramatsu, Koji
Nakamura, Atsuo
Yamashita, Ayano
Kitada, Yusuke
Kakeyama, Masaki
Benno, Yoshimi
Matsumoto, Mitsuharu
Upregulation of colonic luminal polyamines produced by intestinal microbiota delays senescence in mice
title Upregulation of colonic luminal polyamines produced by intestinal microbiota delays senescence in mice
title_full Upregulation of colonic luminal polyamines produced by intestinal microbiota delays senescence in mice
title_fullStr Upregulation of colonic luminal polyamines produced by intestinal microbiota delays senescence in mice
title_full_unstemmed Upregulation of colonic luminal polyamines produced by intestinal microbiota delays senescence in mice
title_short Upregulation of colonic luminal polyamines produced by intestinal microbiota delays senescence in mice
title_sort upregulation of colonic luminal polyamines produced by intestinal microbiota delays senescence in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4070089/
https://www.ncbi.nlm.nih.gov/pubmed/24686447
http://dx.doi.org/10.1038/srep04548
work_keys_str_mv AT kiberyoko upregulationofcolonicluminalpolyaminesproducedbyintestinalmicrobiotadelayssenescenceinmice
AT kuriharashin upregulationofcolonicluminalpolyaminesproducedbyintestinalmicrobiotadelayssenescenceinmice
AT sakaiyumi upregulationofcolonicluminalpolyaminesproducedbyintestinalmicrobiotadelayssenescenceinmice
AT suzukihideyuki upregulationofcolonicluminalpolyaminesproducedbyintestinalmicrobiotadelayssenescenceinmice
AT oogatakushi upregulationofcolonicluminalpolyaminesproducedbyintestinalmicrobiotadelayssenescenceinmice
AT sawakiemiko upregulationofcolonicluminalpolyaminesproducedbyintestinalmicrobiotadelayssenescenceinmice
AT muramatsukoji upregulationofcolonicluminalpolyaminesproducedbyintestinalmicrobiotadelayssenescenceinmice
AT nakamuraatsuo upregulationofcolonicluminalpolyaminesproducedbyintestinalmicrobiotadelayssenescenceinmice
AT yamashitaayano upregulationofcolonicluminalpolyaminesproducedbyintestinalmicrobiotadelayssenescenceinmice
AT kitadayusuke upregulationofcolonicluminalpolyaminesproducedbyintestinalmicrobiotadelayssenescenceinmice
AT kakeyamamasaki upregulationofcolonicluminalpolyaminesproducedbyintestinalmicrobiotadelayssenescenceinmice
AT bennoyoshimi upregulationofcolonicluminalpolyaminesproducedbyintestinalmicrobiotadelayssenescenceinmice
AT matsumotomitsuharu upregulationofcolonicluminalpolyaminesproducedbyintestinalmicrobiotadelayssenescenceinmice