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Establishment of a diabetes mellitus type 1 model in the common marmoset
Common marmosets have attracted considerable attention as a small standard primate model in biomedical research. However, no marmoset diabetes model is available. Here, we established a marmoset diabetes model via the combination of partial pancreatectomy and intravenous streptozotocin (STZ). A part...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6787219/ https://www.ncbi.nlm.nih.gov/pubmed/31601983 http://dx.doi.org/10.1038/s41598-019-51199-5 |
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author | Yuan, Wenji Fukuda, Satsuki Inoue, Takashi Okochi, Hitoshi Sasaki, Erika Shimoda, Masayuki |
author_facet | Yuan, Wenji Fukuda, Satsuki Inoue, Takashi Okochi, Hitoshi Sasaki, Erika Shimoda, Masayuki |
author_sort | Yuan, Wenji |
collection | PubMed |
description | Common marmosets have attracted considerable attention as a small standard primate model in biomedical research. However, no marmoset diabetes model is available. Here, we established a marmoset diabetes model via the combination of partial pancreatectomy and intravenous streptozotocin (STZ). A partial pancreatectomy was performed in 11 common marmosets and multiple STZ doses were intravenously administered. Diabetes was diagnosed upon sustained hyperglycaemia (nonfasting blood glucose level >200 mg/dl). Blood glucose and biochemistry were periodically assessed, in addition to glucose tolerance testing, continual blood glucose determination using a continuous glucose monitoring system, urine testing and histological evaluation. In 8 of the 11 animals (73%), diabetes mellitus was induced. The diabetic marmosets also showed abnormal intravenous and oral glucose tolerance test results. Blood glucose levels decreased in response to human insulin administration. The hyperglycaemic state was irreversible and persisted for more than 3 months, and the animals’ condition was manageable via daily insulin administration. Thus, diabetes can be successfully induced and maintained in the common marmoset via partial pancreatectomy and STZ administration. This protocol effectively generates a valuable animal model for studying disease pathogenesis, risk factors and therapeutic interventions, including islet transplantation. |
format | Online Article Text |
id | pubmed-6787219 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67872192019-10-17 Establishment of a diabetes mellitus type 1 model in the common marmoset Yuan, Wenji Fukuda, Satsuki Inoue, Takashi Okochi, Hitoshi Sasaki, Erika Shimoda, Masayuki Sci Rep Article Common marmosets have attracted considerable attention as a small standard primate model in biomedical research. However, no marmoset diabetes model is available. Here, we established a marmoset diabetes model via the combination of partial pancreatectomy and intravenous streptozotocin (STZ). A partial pancreatectomy was performed in 11 common marmosets and multiple STZ doses were intravenously administered. Diabetes was diagnosed upon sustained hyperglycaemia (nonfasting blood glucose level >200 mg/dl). Blood glucose and biochemistry were periodically assessed, in addition to glucose tolerance testing, continual blood glucose determination using a continuous glucose monitoring system, urine testing and histological evaluation. In 8 of the 11 animals (73%), diabetes mellitus was induced. The diabetic marmosets also showed abnormal intravenous and oral glucose tolerance test results. Blood glucose levels decreased in response to human insulin administration. The hyperglycaemic state was irreversible and persisted for more than 3 months, and the animals’ condition was manageable via daily insulin administration. Thus, diabetes can be successfully induced and maintained in the common marmoset via partial pancreatectomy and STZ administration. This protocol effectively generates a valuable animal model for studying disease pathogenesis, risk factors and therapeutic interventions, including islet transplantation. Nature Publishing Group UK 2019-10-10 /pmc/articles/PMC6787219/ /pubmed/31601983 http://dx.doi.org/10.1038/s41598-019-51199-5 Text en © The Author(s) 2019 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Yuan, Wenji Fukuda, Satsuki Inoue, Takashi Okochi, Hitoshi Sasaki, Erika Shimoda, Masayuki Establishment of a diabetes mellitus type 1 model in the common marmoset |
title | Establishment of a diabetes mellitus type 1 model in the common marmoset |
title_full | Establishment of a diabetes mellitus type 1 model in the common marmoset |
title_fullStr | Establishment of a diabetes mellitus type 1 model in the common marmoset |
title_full_unstemmed | Establishment of a diabetes mellitus type 1 model in the common marmoset |
title_short | Establishment of a diabetes mellitus type 1 model in the common marmoset |
title_sort | establishment of a diabetes mellitus type 1 model in the common marmoset |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6787219/ https://www.ncbi.nlm.nih.gov/pubmed/31601983 http://dx.doi.org/10.1038/s41598-019-51199-5 |
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