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Comparative study on the modulation of incretin and insulin homeostasis by butyrate in chicken and rabbit
The pancreatic secretion of insulin, a key endocrine regulator of metabolism and growth, can be greatly influenced by the gut-derived incretin hormones, namely by GIP (Glucose-dependent Insulinotropic Peptide) and GLP-1 (Glucagon-like Peptide 1). As insulin is a major stimulator of growth, affecting...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6181377/ https://www.ncbi.nlm.nih.gov/pubmed/30308056 http://dx.doi.org/10.1371/journal.pone.0205512 |
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author | Mátis, Gábor Kulcsár, Anna Mackei, Máté Petrilla, Janka Neogrády, Zsuzsanna |
author_facet | Mátis, Gábor Kulcsár, Anna Mackei, Máté Petrilla, Janka Neogrády, Zsuzsanna |
author_sort | Mátis, Gábor |
collection | PubMed |
description | The pancreatic secretion of insulin, a key endocrine regulator of metabolism and growth, can be greatly influenced by the gut-derived incretin hormones, namely by GIP (Glucose-dependent Insulinotropic Peptide) and GLP-1 (Glucagon-like Peptide 1). As insulin is a major stimulator of growth, affecting its producion may be of special importance in food-producing livestock. The aim of the present study was to investigate novel ways of modulating incretin and insulin homeostasis in chickens and rabbits by nutrition, e.g. by oral butyrate application, also studying the mechanisms of incretin action in both species as a comparative approach. Acute oral butyrate challenge significantly decreased plasma GIP levels by approx. 40% in both species: significant interactions of butyrate exposure and incubation time were found in both chickens (P = 0.038 and P = 0.034 at 30 and 60 min following butyrate ingestion [1.25 g/kg BW], respectively) and rabbits (P = 0.036 and P = 0.039 at 30 and 60 min after butyrate ingestion [0.25 g/kg BW], respectively), while plasma GLP-1, insulin and glucose concentrations remained unaffected by butyrate in both species over time. These results are in contrast to butyrate’s stimulating effect on both incretin and insulin secretion in mice, indicating specific, species-dependent differences even among mammalian species. Further, based on the analyzed correlations between the measured endocrine parameters (regardless of the butyrate exposure), it can be assumed that incretins may regulate pancreatic insulin release in rabbits on a partly different way compared to mice, humans and chickens. |
format | Online Article Text |
id | pubmed-6181377 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-61813772018-10-26 Comparative study on the modulation of incretin and insulin homeostasis by butyrate in chicken and rabbit Mátis, Gábor Kulcsár, Anna Mackei, Máté Petrilla, Janka Neogrády, Zsuzsanna PLoS One Research Article The pancreatic secretion of insulin, a key endocrine regulator of metabolism and growth, can be greatly influenced by the gut-derived incretin hormones, namely by GIP (Glucose-dependent Insulinotropic Peptide) and GLP-1 (Glucagon-like Peptide 1). As insulin is a major stimulator of growth, affecting its producion may be of special importance in food-producing livestock. The aim of the present study was to investigate novel ways of modulating incretin and insulin homeostasis in chickens and rabbits by nutrition, e.g. by oral butyrate application, also studying the mechanisms of incretin action in both species as a comparative approach. Acute oral butyrate challenge significantly decreased plasma GIP levels by approx. 40% in both species: significant interactions of butyrate exposure and incubation time were found in both chickens (P = 0.038 and P = 0.034 at 30 and 60 min following butyrate ingestion [1.25 g/kg BW], respectively) and rabbits (P = 0.036 and P = 0.039 at 30 and 60 min after butyrate ingestion [0.25 g/kg BW], respectively), while plasma GLP-1, insulin and glucose concentrations remained unaffected by butyrate in both species over time. These results are in contrast to butyrate’s stimulating effect on both incretin and insulin secretion in mice, indicating specific, species-dependent differences even among mammalian species. Further, based on the analyzed correlations between the measured endocrine parameters (regardless of the butyrate exposure), it can be assumed that incretins may regulate pancreatic insulin release in rabbits on a partly different way compared to mice, humans and chickens. Public Library of Science 2018-10-11 /pmc/articles/PMC6181377/ /pubmed/30308056 http://dx.doi.org/10.1371/journal.pone.0205512 Text en © 2018 Mátis et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Mátis, Gábor Kulcsár, Anna Mackei, Máté Petrilla, Janka Neogrády, Zsuzsanna Comparative study on the modulation of incretin and insulin homeostasis by butyrate in chicken and rabbit |
title | Comparative study on the modulation of incretin and insulin homeostasis by butyrate in chicken and rabbit |
title_full | Comparative study on the modulation of incretin and insulin homeostasis by butyrate in chicken and rabbit |
title_fullStr | Comparative study on the modulation of incretin and insulin homeostasis by butyrate in chicken and rabbit |
title_full_unstemmed | Comparative study on the modulation of incretin and insulin homeostasis by butyrate in chicken and rabbit |
title_short | Comparative study on the modulation of incretin and insulin homeostasis by butyrate in chicken and rabbit |
title_sort | comparative study on the modulation of incretin and insulin homeostasis by butyrate in chicken and rabbit |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6181377/ https://www.ncbi.nlm.nih.gov/pubmed/30308056 http://dx.doi.org/10.1371/journal.pone.0205512 |
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