Characterization of Diabetic Neuropathy in the Zucker Diabetic Sprague-Dawley Rat: A New Animal Model for Type 2 Diabetes

Recently a new rat model for type 2 diabetes the Zucker diabetic Sprague-Dawley (ZDSD/Pco) was created. In this study we sought to characterize the development of diabetic neuropathy in ZDSD rats using age-matched Sprague-Dawley rats as a control. Rats were examined at 34 weeks of age 12 weeks after...

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Main Authors: Eric P. Davidson, Lawrence J. Coppey, Amey Holmes, Sergey Lupachyk, Brian L. Dake, Christine L. Oltman, Richard G. Peterson, Mark A. Yorek
Format: Article
Language:English
Published: Wiley 2014-01-01
Series:Journal of Diabetes Research
Online Access:http://dx.doi.org/10.1155/2014/714273
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author Eric P. Davidson
Lawrence J. Coppey
Amey Holmes
Sergey Lupachyk
Brian L. Dake
Christine L. Oltman
Richard G. Peterson
Mark A. Yorek
author_facet Eric P. Davidson
Lawrence J. Coppey
Amey Holmes
Sergey Lupachyk
Brian L. Dake
Christine L. Oltman
Richard G. Peterson
Mark A. Yorek
author_sort Eric P. Davidson
collection DOAJ
description Recently a new rat model for type 2 diabetes the Zucker diabetic Sprague-Dawley (ZDSD/Pco) was created. In this study we sought to characterize the development of diabetic neuropathy in ZDSD rats using age-matched Sprague-Dawley rats as a control. Rats were examined at 34 weeks of age 12 weeks after the onset of hyperglycemia in ZDSD rats. At this time ZDSD rats were severely insulin resistant with slowing of both motor and sensory nerve conduction velocities. ZDSD rats also had fatty livers, elevated serum free fatty acids, triglycerides, and cholesterol, and elevated sciatic nerve nitrotyrosine levels. The corneas of ZDSD rats exhibited a decrease in subbasal epithelial corneal nerves and sensitivity. ZDSD rats were hypoalgesic but intraepidermal nerve fibers in the skin of the hindpaw were normal compared to Sprague-Dawley rats. However, the number of Langerhans cells was decreased. Vascular reactivity of epineurial arterioles, blood vessels that provide circulation to the sciatic nerve, to acetylcholine and calcitonin gene-related peptide was impaired in ZDSD rats. These data indicate that ZDSD rats develop many of the neural complications associated with type 2 diabetes and are a good animal model for preclinical investigations of drug development for diabetic neuropathy.
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spelling doaj-art-1ecf2629e59b4ff0af1f668cc1bc67fe2025-08-20T03:54:57ZengWileyJournal of Diabetes Research2314-67452314-67532014-01-01201410.1155/2014/714273714273Characterization of Diabetic Neuropathy in the Zucker Diabetic Sprague-Dawley Rat: A New Animal Model for Type 2 DiabetesEric P. Davidson0Lawrence J. Coppey1Amey Holmes2Sergey Lupachyk3Brian L. Dake4Christine L. Oltman5Richard G. Peterson6Mark A. Yorek7Department of Internal Medicine, The University of Iowa, Iowa City, IA 52242, USADepartment of Internal Medicine, The University of Iowa, Iowa City, IA 52242, USADepartment of Veterans Affairs Iowa City Health Care System, Iowa City, IA 52246, USADepartment of Internal Medicine, The University of Iowa, Iowa City, IA 52242, USADepartment of Internal Medicine, The University of Iowa, Iowa City, IA 52242, USADepartment of Veterans Affairs Iowa City Health Care System, Iowa City, IA 52246, USAPreClinOmics Inc., Indianapolis, IN 46268, USADepartment of Internal Medicine, The University of Iowa, Iowa City, IA 52242, USARecently a new rat model for type 2 diabetes the Zucker diabetic Sprague-Dawley (ZDSD/Pco) was created. In this study we sought to characterize the development of diabetic neuropathy in ZDSD rats using age-matched Sprague-Dawley rats as a control. Rats were examined at 34 weeks of age 12 weeks after the onset of hyperglycemia in ZDSD rats. At this time ZDSD rats were severely insulin resistant with slowing of both motor and sensory nerve conduction velocities. ZDSD rats also had fatty livers, elevated serum free fatty acids, triglycerides, and cholesterol, and elevated sciatic nerve nitrotyrosine levels. The corneas of ZDSD rats exhibited a decrease in subbasal epithelial corneal nerves and sensitivity. ZDSD rats were hypoalgesic but intraepidermal nerve fibers in the skin of the hindpaw were normal compared to Sprague-Dawley rats. However, the number of Langerhans cells was decreased. Vascular reactivity of epineurial arterioles, blood vessels that provide circulation to the sciatic nerve, to acetylcholine and calcitonin gene-related peptide was impaired in ZDSD rats. These data indicate that ZDSD rats develop many of the neural complications associated with type 2 diabetes and are a good animal model for preclinical investigations of drug development for diabetic neuropathy.http://dx.doi.org/10.1155/2014/714273
spellingShingle Eric P. Davidson
Lawrence J. Coppey
Amey Holmes
Sergey Lupachyk
Brian L. Dake
Christine L. Oltman
Richard G. Peterson
Mark A. Yorek
Characterization of Diabetic Neuropathy in the Zucker Diabetic Sprague-Dawley Rat: A New Animal Model for Type 2 Diabetes
Journal of Diabetes Research
title Characterization of Diabetic Neuropathy in the Zucker Diabetic Sprague-Dawley Rat: A New Animal Model for Type 2 Diabetes
title_full Characterization of Diabetic Neuropathy in the Zucker Diabetic Sprague-Dawley Rat: A New Animal Model for Type 2 Diabetes
title_fullStr Characterization of Diabetic Neuropathy in the Zucker Diabetic Sprague-Dawley Rat: A New Animal Model for Type 2 Diabetes
title_full_unstemmed Characterization of Diabetic Neuropathy in the Zucker Diabetic Sprague-Dawley Rat: A New Animal Model for Type 2 Diabetes
title_short Characterization of Diabetic Neuropathy in the Zucker Diabetic Sprague-Dawley Rat: A New Animal Model for Type 2 Diabetes
title_sort characterization of diabetic neuropathy in the zucker diabetic sprague dawley rat a new animal model for type 2 diabetes
url http://dx.doi.org/10.1155/2014/714273
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