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Morphological and biochemical changes in the pancreas associated with acute systemic hypoxia
This study aimed to investigate the changes associated with acute systemic hypoxia in the endocrine system, particularly in pancreatic tissues. The investigation was based on macroscopic, pathohistological, biochemical, and molecular biological findings in cell lines and human cadavers. The results...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Singapore
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7900369/ https://www.ncbi.nlm.nih.gov/pubmed/33532907 http://dx.doi.org/10.1007/s13577-020-00481-0 |
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author | Morioka, Fumiya Tani, Naoto Ikeda, Tomoya Hirokawa, Tatsuya Ikeda, Kei Shida, Alissa Aoki, Yayoi Ishikawa, Takaki |
author_facet | Morioka, Fumiya Tani, Naoto Ikeda, Tomoya Hirokawa, Tatsuya Ikeda, Kei Shida, Alissa Aoki, Yayoi Ishikawa, Takaki |
author_sort | Morioka, Fumiya |
collection | PubMed |
description | This study aimed to investigate the changes associated with acute systemic hypoxia in the endocrine system, particularly in pancreatic tissues. The investigation was based on macroscopic, pathohistological, biochemical, and molecular biological findings in cell lines and human cadavers. The results showed that cases of death due to asphyxia more frequently showed severe subcapsular/interstitial hemorrhage versus the other causes of death. Histological examination showed that asphyxia cases were associated with severe morphological changes. Although measured insulin levels in the asphyxia were higher compared to other causes of death, no differences were noted for the glucagon and amylase levels with regard to the cause of death. Increased blood insulin levels were not associated with macro- and micromorphological changes, and did not show any association with glucose or cortisol levels. The experiment conducted under hypoxic conditions in cultured cells demonstrated that insulin mRNA expression and insulin protein levels peaked at 10 min after hypoxia exposure. However, there were no changes in either the amylase mRNA or protein levels. Corticosterone level peaked at 120 min after exposure to hypoxic conditions. Overall, acute systemic hypoxic conditions can directly affect the mechanisms involved in pancreatic insulin secretion. |
format | Online Article Text |
id | pubmed-7900369 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Singapore |
record_format | MEDLINE/PubMed |
spelling | pubmed-79003692021-03-05 Morphological and biochemical changes in the pancreas associated with acute systemic hypoxia Morioka, Fumiya Tani, Naoto Ikeda, Tomoya Hirokawa, Tatsuya Ikeda, Kei Shida, Alissa Aoki, Yayoi Ishikawa, Takaki Hum Cell Research Article This study aimed to investigate the changes associated with acute systemic hypoxia in the endocrine system, particularly in pancreatic tissues. The investigation was based on macroscopic, pathohistological, biochemical, and molecular biological findings in cell lines and human cadavers. The results showed that cases of death due to asphyxia more frequently showed severe subcapsular/interstitial hemorrhage versus the other causes of death. Histological examination showed that asphyxia cases were associated with severe morphological changes. Although measured insulin levels in the asphyxia were higher compared to other causes of death, no differences were noted for the glucagon and amylase levels with regard to the cause of death. Increased blood insulin levels were not associated with macro- and micromorphological changes, and did not show any association with glucose or cortisol levels. The experiment conducted under hypoxic conditions in cultured cells demonstrated that insulin mRNA expression and insulin protein levels peaked at 10 min after hypoxia exposure. However, there were no changes in either the amylase mRNA or protein levels. Corticosterone level peaked at 120 min after exposure to hypoxic conditions. Overall, acute systemic hypoxic conditions can directly affect the mechanisms involved in pancreatic insulin secretion. Springer Singapore 2021-02-02 2021 /pmc/articles/PMC7900369/ /pubmed/33532907 http://dx.doi.org/10.1007/s13577-020-00481-0 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Article Morioka, Fumiya Tani, Naoto Ikeda, Tomoya Hirokawa, Tatsuya Ikeda, Kei Shida, Alissa Aoki, Yayoi Ishikawa, Takaki Morphological and biochemical changes in the pancreas associated with acute systemic hypoxia |
title | Morphological and biochemical changes in the pancreas associated with acute systemic hypoxia |
title_full | Morphological and biochemical changes in the pancreas associated with acute systemic hypoxia |
title_fullStr | Morphological and biochemical changes in the pancreas associated with acute systemic hypoxia |
title_full_unstemmed | Morphological and biochemical changes in the pancreas associated with acute systemic hypoxia |
title_short | Morphological and biochemical changes in the pancreas associated with acute systemic hypoxia |
title_sort | morphological and biochemical changes in the pancreas associated with acute systemic hypoxia |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7900369/ https://www.ncbi.nlm.nih.gov/pubmed/33532907 http://dx.doi.org/10.1007/s13577-020-00481-0 |
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