Feeding with resistant maltodextrin suppresses excessive calorie intake in a high-fat diet, mediated by changes in mouse gut microbiota composition, appetite-related gut hormone secretion, and neuropeptide transcriptional levels

Consuming resistant maltodextrin (RMD) decreases food intake and increase appetite-related gut hormones, but the underlying mechanisms have remained unknown. Therefore, we aimed to elucidate the mechanisms underlying the effects of RMD feeding on food intake (appetite) using Institute of Cancer Rese...

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Main Authors: Kaede Ito, Atsushi Haraguchi, Shuhei Sato, Masataka Sekiguchi, Hiroyuki Sasaki, Conn Ryan, Yijin Lyu, Shigenobu Shibata
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-04-01
Series:Frontiers in Microbiomes
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/frmbi.2023.1149808/full
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author Kaede Ito
Atsushi Haraguchi
Shuhei Sato
Masataka Sekiguchi
Hiroyuki Sasaki
Conn Ryan
Yijin Lyu
Shigenobu Shibata
author_facet Kaede Ito
Atsushi Haraguchi
Shuhei Sato
Masataka Sekiguchi
Hiroyuki Sasaki
Conn Ryan
Yijin Lyu
Shigenobu Shibata
author_sort Kaede Ito
collection DOAJ
description Consuming resistant maltodextrin (RMD) decreases food intake and increase appetite-related gut hormones, but the underlying mechanisms have remained unknown. Therefore, we aimed to elucidate the mechanisms underlying the effects of RMD feeding on food intake (appetite) using Institute of Cancer Research male mice fed with a high-fat diet (HFD-cellulose group) or HFD in which cellulose was replaced with RMD (HFD-RMD group). Feeding mice with an HFD-RMD for approximately 8 weeks inhibited excessive calorie intake and altered the gut microbiota composition. Excessive calorie intake was inhibited for several days in mice fed only with an HFD-cellulose and transplanted with fecal microbiota from the HFD-RMD group (FMT-HFD-RMD group). Moreover, in the HFD-RMD and FMT-HFD-RMD groups, serum active glucagon-like peptide (GLP)-1 and peptide tyrosine tyrosine (PYY) levels were significantly higher, and appetite-related neuropeptide gene transcription in the hypothalamus were significantly altered, compared with the HFD-cellulose and FMT-HFD-cellulose groups. These results suggested that the long-term RMD intake changed the gut microbiota composition, increased the GLP-1 and PYY secretion, and altered the appetite-related neuropeptide gene transcription in the hypothalamus, leading to suppressed excessive calorie intake in an HFD.
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spelling doaj.art-d7ebe1f6157a4f538eaa330a2f7765a42023-04-21T04:39:03ZengFrontiers Media S.A.Frontiers in Microbiomes2813-43382023-04-01210.3389/frmbi.2023.11498081149808Feeding with resistant maltodextrin suppresses excessive calorie intake in a high-fat diet, mediated by changes in mouse gut microbiota composition, appetite-related gut hormone secretion, and neuropeptide transcriptional levelsKaede ItoAtsushi HaraguchiShuhei SatoMasataka SekiguchiHiroyuki SasakiConn RyanYijin LyuShigenobu ShibataConsuming resistant maltodextrin (RMD) decreases food intake and increase appetite-related gut hormones, but the underlying mechanisms have remained unknown. Therefore, we aimed to elucidate the mechanisms underlying the effects of RMD feeding on food intake (appetite) using Institute of Cancer Research male mice fed with a high-fat diet (HFD-cellulose group) or HFD in which cellulose was replaced with RMD (HFD-RMD group). Feeding mice with an HFD-RMD for approximately 8 weeks inhibited excessive calorie intake and altered the gut microbiota composition. Excessive calorie intake was inhibited for several days in mice fed only with an HFD-cellulose and transplanted with fecal microbiota from the HFD-RMD group (FMT-HFD-RMD group). Moreover, in the HFD-RMD and FMT-HFD-RMD groups, serum active glucagon-like peptide (GLP)-1 and peptide tyrosine tyrosine (PYY) levels were significantly higher, and appetite-related neuropeptide gene transcription in the hypothalamus were significantly altered, compared with the HFD-cellulose and FMT-HFD-cellulose groups. These results suggested that the long-term RMD intake changed the gut microbiota composition, increased the GLP-1 and PYY secretion, and altered the appetite-related neuropeptide gene transcription in the hypothalamus, leading to suppressed excessive calorie intake in an HFD.https://www.frontiersin.org/articles/10.3389/frmbi.2023.1149808/fullgut microbiota compositionappetite and food intakeappetite-related gut hormonesappetite-related neuropeptidesfecal microbiota transplantation (FMT)resistant maltodextrin
spellingShingle Kaede Ito
Atsushi Haraguchi
Shuhei Sato
Masataka Sekiguchi
Hiroyuki Sasaki
Conn Ryan
Yijin Lyu
Shigenobu Shibata
Feeding with resistant maltodextrin suppresses excessive calorie intake in a high-fat diet, mediated by changes in mouse gut microbiota composition, appetite-related gut hormone secretion, and neuropeptide transcriptional levels
Frontiers in Microbiomes
gut microbiota composition
appetite and food intake
appetite-related gut hormones
appetite-related neuropeptides
fecal microbiota transplantation (FMT)
resistant maltodextrin
title Feeding with resistant maltodextrin suppresses excessive calorie intake in a high-fat diet, mediated by changes in mouse gut microbiota composition, appetite-related gut hormone secretion, and neuropeptide transcriptional levels
title_full Feeding with resistant maltodextrin suppresses excessive calorie intake in a high-fat diet, mediated by changes in mouse gut microbiota composition, appetite-related gut hormone secretion, and neuropeptide transcriptional levels
title_fullStr Feeding with resistant maltodextrin suppresses excessive calorie intake in a high-fat diet, mediated by changes in mouse gut microbiota composition, appetite-related gut hormone secretion, and neuropeptide transcriptional levels
title_full_unstemmed Feeding with resistant maltodextrin suppresses excessive calorie intake in a high-fat diet, mediated by changes in mouse gut microbiota composition, appetite-related gut hormone secretion, and neuropeptide transcriptional levels
title_short Feeding with resistant maltodextrin suppresses excessive calorie intake in a high-fat diet, mediated by changes in mouse gut microbiota composition, appetite-related gut hormone secretion, and neuropeptide transcriptional levels
title_sort feeding with resistant maltodextrin suppresses excessive calorie intake in a high fat diet mediated by changes in mouse gut microbiota composition appetite related gut hormone secretion and neuropeptide transcriptional levels
topic gut microbiota composition
appetite and food intake
appetite-related gut hormones
appetite-related neuropeptides
fecal microbiota transplantation (FMT)
resistant maltodextrin
url https://www.frontiersin.org/articles/10.3389/frmbi.2023.1149808/full
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