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C-Peptide-Based Assessment of Insulin Secretion in the Zucker Fatty Rat: A Modelistic Study
A C-peptide-based assessment of β-cell function was performed here in the Zucker fatty rat, a suitable animal model of human metabolic syndrome. To this aim, a 90-min intravenous glucose tolerance test (IVGTT) was performed in seven Zucker fatty rats (ZFR), 7-to-9week-old, and seven age-matched Zuck...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4418729/ https://www.ncbi.nlm.nih.gov/pubmed/25938808 http://dx.doi.org/10.1371/journal.pone.0125252 |
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author | Di Nardo, Francesco Cogo, Carla E. Faelli, Emanuela Morettini, Micaela Burattini, Laura Ruggeri, Piero |
author_facet | Di Nardo, Francesco Cogo, Carla E. Faelli, Emanuela Morettini, Micaela Burattini, Laura Ruggeri, Piero |
author_sort | Di Nardo, Francesco |
collection | PubMed |
description | A C-peptide-based assessment of β-cell function was performed here in the Zucker fatty rat, a suitable animal model of human metabolic syndrome. To this aim, a 90-min intravenous glucose tolerance test (IVGTT) was performed in seven Zucker fatty rats (ZFR), 7-to-9week-old, and seven age-matched Zucker lean rats (ZLR). The minimal model of C-peptide (CPMM), originally introduced for humans, was adapted to Zucker rats and then applied to interpret IVGTT data. For a comprehensive evaluation of glucose tolerance in ZFR, CPMM was applied in combination with the minimal model of glucose kinetics (GKMM). Our results showed that the present CPMM-based interpretation of data is able to: 1) provide a suitable fit of C-Peptide data; 2) achieve a satisfactory estimation of parameters of interest 3) quantify both insulin secretion by estimating the time course of pre-hepatic secretion rate, SR(t), and total insulin secretion, TIS, and pancreatic sensitivity by means of three specific indexes of β-cell responsiveness to glucose stimulus (first-phase, Ф(1), second-phase, Ф(2), and steady-state, Ф(ss), never assessed in Zucker rats before; 4) detect the significant enhancement of insulin secretion in the ZFR, in face of a severe insulin-resistant state, previously observed only using a purely experimental approach. Thus, the methodology presented here represents a reliable tool to assess β-cell function in the Zucker rat, and opens new possibilities for the quantification of further processes involved in glucose homeostasis such as the hepatic insulin degradation. |
format | Online Article Text |
id | pubmed-4418729 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-44187292015-05-12 C-Peptide-Based Assessment of Insulin Secretion in the Zucker Fatty Rat: A Modelistic Study Di Nardo, Francesco Cogo, Carla E. Faelli, Emanuela Morettini, Micaela Burattini, Laura Ruggeri, Piero PLoS One Research Article A C-peptide-based assessment of β-cell function was performed here in the Zucker fatty rat, a suitable animal model of human metabolic syndrome. To this aim, a 90-min intravenous glucose tolerance test (IVGTT) was performed in seven Zucker fatty rats (ZFR), 7-to-9week-old, and seven age-matched Zucker lean rats (ZLR). The minimal model of C-peptide (CPMM), originally introduced for humans, was adapted to Zucker rats and then applied to interpret IVGTT data. For a comprehensive evaluation of glucose tolerance in ZFR, CPMM was applied in combination with the minimal model of glucose kinetics (GKMM). Our results showed that the present CPMM-based interpretation of data is able to: 1) provide a suitable fit of C-Peptide data; 2) achieve a satisfactory estimation of parameters of interest 3) quantify both insulin secretion by estimating the time course of pre-hepatic secretion rate, SR(t), and total insulin secretion, TIS, and pancreatic sensitivity by means of three specific indexes of β-cell responsiveness to glucose stimulus (first-phase, Ф(1), second-phase, Ф(2), and steady-state, Ф(ss), never assessed in Zucker rats before; 4) detect the significant enhancement of insulin secretion in the ZFR, in face of a severe insulin-resistant state, previously observed only using a purely experimental approach. Thus, the methodology presented here represents a reliable tool to assess β-cell function in the Zucker rat, and opens new possibilities for the quantification of further processes involved in glucose homeostasis such as the hepatic insulin degradation. Public Library of Science 2015-05-04 /pmc/articles/PMC4418729/ /pubmed/25938808 http://dx.doi.org/10.1371/journal.pone.0125252 Text en © 2015 Di Nardo 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Di Nardo, Francesco Cogo, Carla E. Faelli, Emanuela Morettini, Micaela Burattini, Laura Ruggeri, Piero C-Peptide-Based Assessment of Insulin Secretion in the Zucker Fatty Rat: A Modelistic Study |
title | C-Peptide-Based Assessment of Insulin Secretion in the Zucker Fatty Rat: A Modelistic Study |
title_full | C-Peptide-Based Assessment of Insulin Secretion in the Zucker Fatty Rat: A Modelistic Study |
title_fullStr | C-Peptide-Based Assessment of Insulin Secretion in the Zucker Fatty Rat: A Modelistic Study |
title_full_unstemmed | C-Peptide-Based Assessment of Insulin Secretion in the Zucker Fatty Rat: A Modelistic Study |
title_short | C-Peptide-Based Assessment of Insulin Secretion in the Zucker Fatty Rat: A Modelistic Study |
title_sort | c-peptide-based assessment of insulin secretion in the zucker fatty rat: a modelistic study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4418729/ https://www.ncbi.nlm.nih.gov/pubmed/25938808 http://dx.doi.org/10.1371/journal.pone.0125252 |
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