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GSPE Pre-Treatment Exerts Long-Lasting Preventive Effects against Aging-Induced Changes in the Colonic Enterohormone Profile of Female Rats

The impact that healthy aging can have on society has raised great interest in understanding aging mechanisms. However, the effects this biological process may have on the gastrointestinal tract (GIT) have not yet been fully described. Results in relation to changes observed in the enteroendocrine s...

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Autores principales: Miguéns-Gómez, Alba, Sierra-Cruz, Marta, Blay, M. Teresa, Rodríguez-Gallego, Esther, Beltrán-Debón, Raúl, Terra, Ximena, Pinent, Montserrat, Ardévol, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10177949/
https://www.ncbi.nlm.nih.gov/pubmed/37175514
http://dx.doi.org/10.3390/ijms24097807
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author Miguéns-Gómez, Alba
Sierra-Cruz, Marta
Blay, M. Teresa
Rodríguez-Gallego, Esther
Beltrán-Debón, Raúl
Terra, Ximena
Pinent, Montserrat
Ardévol, Anna
author_facet Miguéns-Gómez, Alba
Sierra-Cruz, Marta
Blay, M. Teresa
Rodríguez-Gallego, Esther
Beltrán-Debón, Raúl
Terra, Ximena
Pinent, Montserrat
Ardévol, Anna
author_sort Miguéns-Gómez, Alba
collection PubMed
description The impact that healthy aging can have on society has raised great interest in understanding aging mechanisms. However, the effects this biological process may have on the gastrointestinal tract (GIT) have not yet been fully described. Results in relation to changes observed in the enteroendocrine system along the GIT are controversial. Grape seed proanthocyanidin extracts (GSPE) have been shown to protect against several pathologies associated with aging. Based on previous results, we hypothesized that a GSPE pre-treatment could prevent the aging processes that affect the enteroendocrine system. To test this hypothesis, we treated 21-month-old female rats with GSPE for 10 days. Eleven weeks after the treatment, we analyzed the effects of GSPE by comparing these aged animals with young animals. Aging induced a greater endocrine response to stimulation in the upper GIT segments (cholecystokinin (CCK) and glucagon-like peptide-1 (GLP-1)), a decrease in the mRNA abundance of GLP-1, peptide YY (PYY) and chromogranin A (ChgA) in the colon, and an increase in colonic butyrate. GSPE-treated rats were protected against a decrease in enterohormone expression in the colon. This effect is not directly related to the abundance of microbiome or short-chain fatty acids (SCFA) at this location. GSPE may therefore be effective in preventing a decrease in the colonic abundance of enterohormone expression induced by aging.
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spelling pubmed-101779492023-05-13 GSPE Pre-Treatment Exerts Long-Lasting Preventive Effects against Aging-Induced Changes in the Colonic Enterohormone Profile of Female Rats Miguéns-Gómez, Alba Sierra-Cruz, Marta Blay, M. Teresa Rodríguez-Gallego, Esther Beltrán-Debón, Raúl Terra, Ximena Pinent, Montserrat Ardévol, Anna Int J Mol Sci Article The impact that healthy aging can have on society has raised great interest in understanding aging mechanisms. However, the effects this biological process may have on the gastrointestinal tract (GIT) have not yet been fully described. Results in relation to changes observed in the enteroendocrine system along the GIT are controversial. Grape seed proanthocyanidin extracts (GSPE) have been shown to protect against several pathologies associated with aging. Based on previous results, we hypothesized that a GSPE pre-treatment could prevent the aging processes that affect the enteroendocrine system. To test this hypothesis, we treated 21-month-old female rats with GSPE for 10 days. Eleven weeks after the treatment, we analyzed the effects of GSPE by comparing these aged animals with young animals. Aging induced a greater endocrine response to stimulation in the upper GIT segments (cholecystokinin (CCK) and glucagon-like peptide-1 (GLP-1)), a decrease in the mRNA abundance of GLP-1, peptide YY (PYY) and chromogranin A (ChgA) in the colon, and an increase in colonic butyrate. GSPE-treated rats were protected against a decrease in enterohormone expression in the colon. This effect is not directly related to the abundance of microbiome or short-chain fatty acids (SCFA) at this location. GSPE may therefore be effective in preventing a decrease in the colonic abundance of enterohormone expression induced by aging. MDPI 2023-04-25 /pmc/articles/PMC10177949/ /pubmed/37175514 http://dx.doi.org/10.3390/ijms24097807 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Miguéns-Gómez, Alba
Sierra-Cruz, Marta
Blay, M. Teresa
Rodríguez-Gallego, Esther
Beltrán-Debón, Raúl
Terra, Ximena
Pinent, Montserrat
Ardévol, Anna
GSPE Pre-Treatment Exerts Long-Lasting Preventive Effects against Aging-Induced Changes in the Colonic Enterohormone Profile of Female Rats
title GSPE Pre-Treatment Exerts Long-Lasting Preventive Effects against Aging-Induced Changes in the Colonic Enterohormone Profile of Female Rats
title_full GSPE Pre-Treatment Exerts Long-Lasting Preventive Effects against Aging-Induced Changes in the Colonic Enterohormone Profile of Female Rats
title_fullStr GSPE Pre-Treatment Exerts Long-Lasting Preventive Effects against Aging-Induced Changes in the Colonic Enterohormone Profile of Female Rats
title_full_unstemmed GSPE Pre-Treatment Exerts Long-Lasting Preventive Effects against Aging-Induced Changes in the Colonic Enterohormone Profile of Female Rats
title_short GSPE Pre-Treatment Exerts Long-Lasting Preventive Effects against Aging-Induced Changes in the Colonic Enterohormone Profile of Female Rats
title_sort gspe pre-treatment exerts long-lasting preventive effects against aging-induced changes in the colonic enterohormone profile of female rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10177949/
https://www.ncbi.nlm.nih.gov/pubmed/37175514
http://dx.doi.org/10.3390/ijms24097807
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