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Feasibility of large experimental animal models in testing novel therapeutic strategies for diabetes

Diabetes is among the top 10 causes of death in adults and caused approximately four million deaths worldwide in 2017. The incidence and prevalence of diabetes is predicted to increase. To alleviate this potentially severe situation, safer and more effective therapeutics are urgently required. Mice...

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Autores principales: Nagaya, Masaki, Hasegawa, Koki, Uchikura, Ayuko, Nakano, Kazuaki, Watanabe, Masahito, Umeyama, Kazuhiro, Matsunari, Hitomi, Osafune, Kenji, Kobayashi, Eiji, Nakauchi, Hiromitsu, Nagashima, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8040081/
https://www.ncbi.nlm.nih.gov/pubmed/33889282
http://dx.doi.org/10.4239/wjd.v12.i4.306
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author Nagaya, Masaki
Hasegawa, Koki
Uchikura, Ayuko
Nakano, Kazuaki
Watanabe, Masahito
Umeyama, Kazuhiro
Matsunari, Hitomi
Osafune, Kenji
Kobayashi, Eiji
Nakauchi, Hiromitsu
Nagashima, Hiroshi
author_facet Nagaya, Masaki
Hasegawa, Koki
Uchikura, Ayuko
Nakano, Kazuaki
Watanabe, Masahito
Umeyama, Kazuhiro
Matsunari, Hitomi
Osafune, Kenji
Kobayashi, Eiji
Nakauchi, Hiromitsu
Nagashima, Hiroshi
author_sort Nagaya, Masaki
collection PubMed
description Diabetes is among the top 10 causes of death in adults and caused approximately four million deaths worldwide in 2017. The incidence and prevalence of diabetes is predicted to increase. To alleviate this potentially severe situation, safer and more effective therapeutics are urgently required. Mice have long been the mainstay as preclinical models for basic research on diabetes, although they are not ideally suited for translating basic knowledge into clinical applications. To validate and optimize novel therapeutics for safe application in humans, an appropriate large animal model is needed. Large animals, especially pigs, are well suited for biomedical research and share many similarities with humans, including body size, anatomical features, physiology, and pathophysiology. Moreover, pigs already play an important role in translational studies, including clinical trials for xenotransplantation. Progress in genetic engineering over the past few decades has facilitated the development of transgenic animals, including porcine models of diabetes. This article discusses features that attest to the attractiveness of genetically modified porcine models of diabetes for testing novel treatment strategies using recent technical advances.
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spelling pubmed-80400812021-04-21 Feasibility of large experimental animal models in testing novel therapeutic strategies for diabetes Nagaya, Masaki Hasegawa, Koki Uchikura, Ayuko Nakano, Kazuaki Watanabe, Masahito Umeyama, Kazuhiro Matsunari, Hitomi Osafune, Kenji Kobayashi, Eiji Nakauchi, Hiromitsu Nagashima, Hiroshi World J Diabetes Therapeutic and Diagnostic Guidelines Diabetes is among the top 10 causes of death in adults and caused approximately four million deaths worldwide in 2017. The incidence and prevalence of diabetes is predicted to increase. To alleviate this potentially severe situation, safer and more effective therapeutics are urgently required. Mice have long been the mainstay as preclinical models for basic research on diabetes, although they are not ideally suited for translating basic knowledge into clinical applications. To validate and optimize novel therapeutics for safe application in humans, an appropriate large animal model is needed. Large animals, especially pigs, are well suited for biomedical research and share many similarities with humans, including body size, anatomical features, physiology, and pathophysiology. Moreover, pigs already play an important role in translational studies, including clinical trials for xenotransplantation. Progress in genetic engineering over the past few decades has facilitated the development of transgenic animals, including porcine models of diabetes. This article discusses features that attest to the attractiveness of genetically modified porcine models of diabetes for testing novel treatment strategies using recent technical advances. Baishideng Publishing Group Inc 2021-04-15 2021-04-15 /pmc/articles/PMC8040081/ /pubmed/33889282 http://dx.doi.org/10.4239/wjd.v12.i4.306 Text en ©The Author(s) 2021. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/Licenses/by-nc/4.0/
spellingShingle Therapeutic and Diagnostic Guidelines
Nagaya, Masaki
Hasegawa, Koki
Uchikura, Ayuko
Nakano, Kazuaki
Watanabe, Masahito
Umeyama, Kazuhiro
Matsunari, Hitomi
Osafune, Kenji
Kobayashi, Eiji
Nakauchi, Hiromitsu
Nagashima, Hiroshi
Feasibility of large experimental animal models in testing novel therapeutic strategies for diabetes
title Feasibility of large experimental animal models in testing novel therapeutic strategies for diabetes
title_full Feasibility of large experimental animal models in testing novel therapeutic strategies for diabetes
title_fullStr Feasibility of large experimental animal models in testing novel therapeutic strategies for diabetes
title_full_unstemmed Feasibility of large experimental animal models in testing novel therapeutic strategies for diabetes
title_short Feasibility of large experimental animal models in testing novel therapeutic strategies for diabetes
title_sort feasibility of large experimental animal models in testing novel therapeutic strategies for diabetes
topic Therapeutic and Diagnostic Guidelines
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8040081/
https://www.ncbi.nlm.nih.gov/pubmed/33889282
http://dx.doi.org/10.4239/wjd.v12.i4.306
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