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Helicobacter pylori infection can affect energy modulating hormones and body weight in germ free mice

Helicobacter pylori, is an invariably commensal resident of the gut microbiome associated with gastric ulcer in adults. In addition, these patients also suffered from a low grade inflammation that activates the immune system and thus increased shunting of energy to host defense mechanisms. To assess...

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Autores principales: Khosravi, Yalda, Seow, Shih Wee, Amoyo, Arlaine Anne, Chiow, Kher Hsin, Tan, Tuan Lin, Wong, Whye Yen, Poh, Qian Hui, Sentosa, Ignatius Mario Doli, Bunte, Ralph M., Pettersson, Sven, Loke, Mun Fai, Vadivelu, Jamuna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4348668/
https://www.ncbi.nlm.nih.gov/pubmed/25736205
http://dx.doi.org/10.1038/srep08731
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author Khosravi, Yalda
Seow, Shih Wee
Amoyo, Arlaine Anne
Chiow, Kher Hsin
Tan, Tuan Lin
Wong, Whye Yen
Poh, Qian Hui
Sentosa, Ignatius Mario Doli
Bunte, Ralph M.
Pettersson, Sven
Loke, Mun Fai
Vadivelu, Jamuna
author_facet Khosravi, Yalda
Seow, Shih Wee
Amoyo, Arlaine Anne
Chiow, Kher Hsin
Tan, Tuan Lin
Wong, Whye Yen
Poh, Qian Hui
Sentosa, Ignatius Mario Doli
Bunte, Ralph M.
Pettersson, Sven
Loke, Mun Fai
Vadivelu, Jamuna
author_sort Khosravi, Yalda
collection PubMed
description Helicobacter pylori, is an invariably commensal resident of the gut microbiome associated with gastric ulcer in adults. In addition, these patients also suffered from a low grade inflammation that activates the immune system and thus increased shunting of energy to host defense mechanisms. To assess whether a H. pylori infection could affect growth in early life, we determined the expression levels of selected metabolic gut hormones in germ free (GF) and specific pathogen-free (SPF) mice with and without the presence of H. pylori. Despite H. pylori-infected (SPFH) mice display alteration in host metabolism (elevated levels of leptin, insulin and peptide YY) compared to non-infected SPF mice, their growth curves remained the same. SPFH mice also displayed increased level of eotaxin-1. Interestingly, GF mice infected with H. pylori (GFH) also displayed increased levels of ghrelin and PYY. However, in contrast to SPFH mice, GFH showed reduced weight gain and malnutrition. These preliminary findings show that exposure to H. pylori alters host metabolism early in life; but the commensal microbiota in SPF mice can attenuate the growth retarding effect from H. pylori observed in GF mice. Further investigations of possible additional side effects of H. pylori are highly warranted.
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spelling pubmed-43486682015-03-10 Helicobacter pylori infection can affect energy modulating hormones and body weight in germ free mice Khosravi, Yalda Seow, Shih Wee Amoyo, Arlaine Anne Chiow, Kher Hsin Tan, Tuan Lin Wong, Whye Yen Poh, Qian Hui Sentosa, Ignatius Mario Doli Bunte, Ralph M. Pettersson, Sven Loke, Mun Fai Vadivelu, Jamuna Sci Rep Article Helicobacter pylori, is an invariably commensal resident of the gut microbiome associated with gastric ulcer in adults. In addition, these patients also suffered from a low grade inflammation that activates the immune system and thus increased shunting of energy to host defense mechanisms. To assess whether a H. pylori infection could affect growth in early life, we determined the expression levels of selected metabolic gut hormones in germ free (GF) and specific pathogen-free (SPF) mice with and without the presence of H. pylori. Despite H. pylori-infected (SPFH) mice display alteration in host metabolism (elevated levels of leptin, insulin and peptide YY) compared to non-infected SPF mice, their growth curves remained the same. SPFH mice also displayed increased level of eotaxin-1. Interestingly, GF mice infected with H. pylori (GFH) also displayed increased levels of ghrelin and PYY. However, in contrast to SPFH mice, GFH showed reduced weight gain and malnutrition. These preliminary findings show that exposure to H. pylori alters host metabolism early in life; but the commensal microbiota in SPF mice can attenuate the growth retarding effect from H. pylori observed in GF mice. Further investigations of possible additional side effects of H. pylori are highly warranted. Nature Publishing Group 2015-03-04 /pmc/articles/PMC4348668/ /pubmed/25736205 http://dx.doi.org/10.1038/srep08731 Text en Copyright © 2015, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Khosravi, Yalda
Seow, Shih Wee
Amoyo, Arlaine Anne
Chiow, Kher Hsin
Tan, Tuan Lin
Wong, Whye Yen
Poh, Qian Hui
Sentosa, Ignatius Mario Doli
Bunte, Ralph M.
Pettersson, Sven
Loke, Mun Fai
Vadivelu, Jamuna
Helicobacter pylori infection can affect energy modulating hormones and body weight in germ free mice
title Helicobacter pylori infection can affect energy modulating hormones and body weight in germ free mice
title_full Helicobacter pylori infection can affect energy modulating hormones and body weight in germ free mice
title_fullStr Helicobacter pylori infection can affect energy modulating hormones and body weight in germ free mice
title_full_unstemmed Helicobacter pylori infection can affect energy modulating hormones and body weight in germ free mice
title_short Helicobacter pylori infection can affect energy modulating hormones and body weight in germ free mice
title_sort helicobacter pylori infection can affect energy modulating hormones and body weight in germ free mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4348668/
https://www.ncbi.nlm.nih.gov/pubmed/25736205
http://dx.doi.org/10.1038/srep08731
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