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Histopathological nerve and skeletal muscle changes in rats subjected to persistent insulin-induced hypoglycemia

New insulin analogues with a longer duration of action and a flatter pharmacodynamic profile are developed to improve convenience and safety for diabetic patients. During the nonclinical development of such analogues, safety studies must be conducted in nondiabetic rats, which consequently are rende...

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Autores principales: Jensen, Vivi Flou Hjorth, Mølck, Anne-Marie, Heydenreich, Annette, Jensen, Karin Juul, Bertelsen, Line Olrik, Alifrangis, Lene, Andersen, Lene, Søeborg, Henrik, Chapman, Melissa, Lykkesfeldt, Jens, Bøgh, Ingrid Brück
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japanese Society of Toxicologic Pathology 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4766526/
https://www.ncbi.nlm.nih.gov/pubmed/26989298
http://dx.doi.org/10.1293/tox.2015-0041
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author Jensen, Vivi Flou Hjorth
Mølck, Anne-Marie
Heydenreich, Annette
Jensen, Karin Juul
Bertelsen, Line Olrik
Alifrangis, Lene
Andersen, Lene
Søeborg, Henrik
Chapman, Melissa
Lykkesfeldt, Jens
Bøgh, Ingrid Brück
author_facet Jensen, Vivi Flou Hjorth
Mølck, Anne-Marie
Heydenreich, Annette
Jensen, Karin Juul
Bertelsen, Line Olrik
Alifrangis, Lene
Andersen, Lene
Søeborg, Henrik
Chapman, Melissa
Lykkesfeldt, Jens
Bøgh, Ingrid Brück
author_sort Jensen, Vivi Flou Hjorth
collection PubMed
description New insulin analogues with a longer duration of action and a flatter pharmacodynamic profile are developed to improve convenience and safety for diabetic patients. During the nonclinical development of such analogues, safety studies must be conducted in nondiabetic rats, which consequently are rendered chronically hypoglycemic. A rat comparator model using human insulin would be valuable, as it would enable differentiation between effects related to either persistent insulin-induced hypoglycemia (IIH) or a new analogue per se. Such a model could alleviate the need for an in-study-comparator and thereby reduce the number of animals used during development. Thus, the aims of the present study were i) to develop a preclinical animal model of persistent hypoglycemia in rats using human insulin infusion for four weeks and ii) to investigate histopathological changes in sciatic nerves and quadriceps femoris muscle tissue, as little is known about the response to persistent hypoglycemia in these tissues. Histopathologic changes in insulin-infused animals included axonal degeneration and myofibre degeneration. To our knowledge, this is the first study to show that persistent IIH provokes peripheral nerve and skeletal myofiber degeneration within the same animals. This suggests that the model can serve as a nonclinical comparator model during development of long-acting insulin analogues.
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spelling pubmed-47665262016-03-17 Histopathological nerve and skeletal muscle changes in rats subjected to persistent insulin-induced hypoglycemia Jensen, Vivi Flou Hjorth Mølck, Anne-Marie Heydenreich, Annette Jensen, Karin Juul Bertelsen, Line Olrik Alifrangis, Lene Andersen, Lene Søeborg, Henrik Chapman, Melissa Lykkesfeldt, Jens Bøgh, Ingrid Brück J Toxicol Pathol Original Article New insulin analogues with a longer duration of action and a flatter pharmacodynamic profile are developed to improve convenience and safety for diabetic patients. During the nonclinical development of such analogues, safety studies must be conducted in nondiabetic rats, which consequently are rendered chronically hypoglycemic. A rat comparator model using human insulin would be valuable, as it would enable differentiation between effects related to either persistent insulin-induced hypoglycemia (IIH) or a new analogue per se. Such a model could alleviate the need for an in-study-comparator and thereby reduce the number of animals used during development. Thus, the aims of the present study were i) to develop a preclinical animal model of persistent hypoglycemia in rats using human insulin infusion for four weeks and ii) to investigate histopathological changes in sciatic nerves and quadriceps femoris muscle tissue, as little is known about the response to persistent hypoglycemia in these tissues. Histopathologic changes in insulin-infused animals included axonal degeneration and myofibre degeneration. To our knowledge, this is the first study to show that persistent IIH provokes peripheral nerve and skeletal myofiber degeneration within the same animals. This suggests that the model can serve as a nonclinical comparator model during development of long-acting insulin analogues. Japanese Society of Toxicologic Pathology 2015-10-29 2016-01 /pmc/articles/PMC4766526/ /pubmed/26989298 http://dx.doi.org/10.1293/tox.2015-0041 Text en ©2016 The Japanese Society of Toxicologic Pathology http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License.
spellingShingle Original Article
Jensen, Vivi Flou Hjorth
Mølck, Anne-Marie
Heydenreich, Annette
Jensen, Karin Juul
Bertelsen, Line Olrik
Alifrangis, Lene
Andersen, Lene
Søeborg, Henrik
Chapman, Melissa
Lykkesfeldt, Jens
Bøgh, Ingrid Brück
Histopathological nerve and skeletal muscle changes in rats subjected to persistent insulin-induced hypoglycemia
title Histopathological nerve and skeletal muscle changes in rats subjected to persistent insulin-induced hypoglycemia
title_full Histopathological nerve and skeletal muscle changes in rats subjected to persistent insulin-induced hypoglycemia
title_fullStr Histopathological nerve and skeletal muscle changes in rats subjected to persistent insulin-induced hypoglycemia
title_full_unstemmed Histopathological nerve and skeletal muscle changes in rats subjected to persistent insulin-induced hypoglycemia
title_short Histopathological nerve and skeletal muscle changes in rats subjected to persistent insulin-induced hypoglycemia
title_sort histopathological nerve and skeletal muscle changes in rats subjected to persistent insulin-induced hypoglycemia
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4766526/
https://www.ncbi.nlm.nih.gov/pubmed/26989298
http://dx.doi.org/10.1293/tox.2015-0041
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