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Identification of proteins involved in the pancreatic exocrine by exogenous ghrelin administration in Sprague-Dawley rats
The aims of study were to investigate the effects of intraperitoneal (i.p.) infusion of ghrelin on pancreatic α-amylase outputs and the responses of pancreatic proteins to ghrelin that may relate to the pancreatic exocrine. Six male Sprague-Dawley rats (300 g) were randomly divided into two groups,...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4534188/ https://www.ncbi.nlm.nih.gov/pubmed/26290695 http://dx.doi.org/10.1186/2055-0391-56-6 |
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author | Lee, Kyung-Hoon Wang, Tao Jin, Yong-Cheng Lee, Sang-Bum Oh, Jin-Ju Hwang, Jin-Hee Lim, Ji-Na Lee, Jae-Sung Lee, Hong-Gu |
author_facet | Lee, Kyung-Hoon Wang, Tao Jin, Yong-Cheng Lee, Sang-Bum Oh, Jin-Ju Hwang, Jin-Hee Lim, Ji-Na Lee, Jae-Sung Lee, Hong-Gu |
author_sort | Lee, Kyung-Hoon |
collection | PubMed |
description | The aims of study were to investigate the effects of intraperitoneal (i.p.) infusion of ghrelin on pancreatic α-amylase outputs and the responses of pancreatic proteins to ghrelin that may relate to the pancreatic exocrine. Six male Sprague-Dawley rats (300 g) were randomly divided into two groups, a control group (C, n = 3) and a treatment group (T, 10.0μg/kg BW, n = 3). Blood samples were collected from rat caudal vein once time after one hour injection. The concentrations of plasma ghrelin, cholecystokinin (CCK) and alfa-amylase activity were evaluated by enzyme immunoassay (EIA) kit. Two-dimensional gel electrophoresis (2-DE) analysis was conducted to separate the proteins in pancreas tissue. Results showed that the i.p. infusion of ghrelin at doses of 10.0 μg/kg body weight (BW) increased the plasma ghrelin concentrations (p = 0.07) and elevated the plasma CCK level significantly (p < 0.05). Although there was no statistically significant, the α-amylase activity tended to increase. The proteomics analysis indicated that some pancreatic proteins with various functions were up- or down- regulated compared with control group. In conclusion, ghrelin may have role in the pancreatic exocrine, but the signaling pathway was still not clear. Therefore, much more functional studies focus on these found proteins are needed in the near future. |
format | Online Article Text |
id | pubmed-4534188 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-45341882015-08-19 Identification of proteins involved in the pancreatic exocrine by exogenous ghrelin administration in Sprague-Dawley rats Lee, Kyung-Hoon Wang, Tao Jin, Yong-Cheng Lee, Sang-Bum Oh, Jin-Ju Hwang, Jin-Hee Lim, Ji-Na Lee, Jae-Sung Lee, Hong-Gu J Anim Sci Technol Research The aims of study were to investigate the effects of intraperitoneal (i.p.) infusion of ghrelin on pancreatic α-amylase outputs and the responses of pancreatic proteins to ghrelin that may relate to the pancreatic exocrine. Six male Sprague-Dawley rats (300 g) were randomly divided into two groups, a control group (C, n = 3) and a treatment group (T, 10.0μg/kg BW, n = 3). Blood samples were collected from rat caudal vein once time after one hour injection. The concentrations of plasma ghrelin, cholecystokinin (CCK) and alfa-amylase activity were evaluated by enzyme immunoassay (EIA) kit. Two-dimensional gel electrophoresis (2-DE) analysis was conducted to separate the proteins in pancreas tissue. Results showed that the i.p. infusion of ghrelin at doses of 10.0 μg/kg body weight (BW) increased the plasma ghrelin concentrations (p = 0.07) and elevated the plasma CCK level significantly (p < 0.05). Although there was no statistically significant, the α-amylase activity tended to increase. The proteomics analysis indicated that some pancreatic proteins with various functions were up- or down- regulated compared with control group. In conclusion, ghrelin may have role in the pancreatic exocrine, but the signaling pathway was still not clear. Therefore, much more functional studies focus on these found proteins are needed in the near future. BioMed Central 2014-06-05 /pmc/articles/PMC4534188/ /pubmed/26290695 http://dx.doi.org/10.1186/2055-0391-56-6 Text en © Lee et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. 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 work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Lee, Kyung-Hoon Wang, Tao Jin, Yong-Cheng Lee, Sang-Bum Oh, Jin-Ju Hwang, Jin-Hee Lim, Ji-Na Lee, Jae-Sung Lee, Hong-Gu Identification of proteins involved in the pancreatic exocrine by exogenous ghrelin administration in Sprague-Dawley rats |
title | Identification of proteins involved in the pancreatic exocrine by exogenous ghrelin administration in Sprague-Dawley rats |
title_full | Identification of proteins involved in the pancreatic exocrine by exogenous ghrelin administration in Sprague-Dawley rats |
title_fullStr | Identification of proteins involved in the pancreatic exocrine by exogenous ghrelin administration in Sprague-Dawley rats |
title_full_unstemmed | Identification of proteins involved in the pancreatic exocrine by exogenous ghrelin administration in Sprague-Dawley rats |
title_short | Identification of proteins involved in the pancreatic exocrine by exogenous ghrelin administration in Sprague-Dawley rats |
title_sort | identification of proteins involved in the pancreatic exocrine by exogenous ghrelin administration in sprague-dawley rats |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4534188/ https://www.ncbi.nlm.nih.gov/pubmed/26290695 http://dx.doi.org/10.1186/2055-0391-56-6 |
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