The Roles of Streptozotocin Neurotoxicity and Neutral Endopeptidase in Murine Experimental Diabetic Neuropathy

Author:

Davidson Eric12,Coppey Lawrence12,Lu Bao3,Arballo Victor4,Calcutt Nigel A.4,Gerard Craig3,Yorek Mark12

Affiliation:

1. Department of Veterans Affairs Iowa City Health Care System, University of Iowa, Iowa City, IA 52246, USA

2. Department of Internal Medicine, University of Iowa, Iowa City, IA 52246, USA

3. Ina Sue Perlmutter Laboratory, Department of Pediatrics and Medicine, Harvard Medical School, Children's Hospital, Boston, MA 02115, USA

4. Department of Pathology, University of California San Diego, La Jolla, CA 92093, USA

Abstract

We demonstrated that inhibition of neutral endopeptidase (NEP), a protease that degrades vaso- and neuroactive peptides, improves vascular and neural function in diabetic animal models. In this study we explored the role of NEP in neuropathy related to either insulin-deficient diabetes or diet-induced obesity using NEP deficient (−/−) mice. Initial studies showed that streptozotocin, in the absence of subsequent hyperglycemia, did not induce nerve conduction slowing or paw thermal hypoalgesia. Glucose disposal was impaired in both C57Bl/6 and NEP −/− mice fed a high fat diet. Thermal hypoalgesia and nerve conduction slowing were present in both streptozotocin-diabetic and high fat fed C57Bl/6 mice but not in NEP −/− mice exposed to either streptozotocin-induced diabetes or a high fat diet. These studies suggest that streptozotocin does not induce neurotoxicity in mice and that NEP plays a role in regulating nerve function in insulin-deficient diabetes and diet-induced obesity.

Funder

Juvenile Diabetes Research Foundation International

Publisher

Hindawi Limited

Subject

General Medicine,Endocrinology, Diabetes and Metabolism

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