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Sensory and autonomic function and structure in footpads of a diabetic mouse model
Sensory and autonomic neuropathy affects the majority of type II diabetic patients. Clinically, autonomic evaluation often focuses on sudomotor function yet this is rarely assessed in animal models. We undertook morphological and functional studies to assess large myelinated and small unmyelinated a...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5269750/ https://www.ncbi.nlm.nih.gov/pubmed/28128284 http://dx.doi.org/10.1038/srep41401 |
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author | Liu, Ying Sebastian, Blessan Liu, Ben Zhang, Yiyue Fissel, John A. Pan, Baohan Polydefkis, Michael Farah, Mohamed H. |
author_facet | Liu, Ying Sebastian, Blessan Liu, Ben Zhang, Yiyue Fissel, John A. Pan, Baohan Polydefkis, Michael Farah, Mohamed H. |
author_sort | Liu, Ying |
collection | PubMed |
description | Sensory and autonomic neuropathy affects the majority of type II diabetic patients. Clinically, autonomic evaluation often focuses on sudomotor function yet this is rarely assessed in animal models. We undertook morphological and functional studies to assess large myelinated and small unmyelinated axons in the db/db type II diabetes mouse model. We observed that autonomic innervation of sweat glands in the footpads was significantly reduced in db/db mice compared to control db/+ mice and this deficit was greater compared to reductions in intraepidermal sensory innervation of adjacent epidermis. Additionally, db/db mice formed significantly fewer sweat droplets compared to controls as early as 6 weeks of age, a time when no statistical differences were observed electrophysiologically between db/db and db/+ mice studies of large myelinated sensory and motor nerves. The rate of sweat droplet formation was significantly slower and the sweat droplet size larger and more variable in db/db mice compared to controls. Whereas pilocarpine and glycopyrrolate increased and decreased sweating, respectively, in 6 month-old controls, db/db mice did not respond to pharmacologic manipulations. Our findings indicate autonomic neuropathy is an early and prominent deficit in the db/db model and have implications for the development of therapies for peripheral diabetic neuropathy. |
format | Online Article Text |
id | pubmed-5269750 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-52697502017-02-01 Sensory and autonomic function and structure in footpads of a diabetic mouse model Liu, Ying Sebastian, Blessan Liu, Ben Zhang, Yiyue Fissel, John A. Pan, Baohan Polydefkis, Michael Farah, Mohamed H. Sci Rep Article Sensory and autonomic neuropathy affects the majority of type II diabetic patients. Clinically, autonomic evaluation often focuses on sudomotor function yet this is rarely assessed in animal models. We undertook morphological and functional studies to assess large myelinated and small unmyelinated axons in the db/db type II diabetes mouse model. We observed that autonomic innervation of sweat glands in the footpads was significantly reduced in db/db mice compared to control db/+ mice and this deficit was greater compared to reductions in intraepidermal sensory innervation of adjacent epidermis. Additionally, db/db mice formed significantly fewer sweat droplets compared to controls as early as 6 weeks of age, a time when no statistical differences were observed electrophysiologically between db/db and db/+ mice studies of large myelinated sensory and motor nerves. The rate of sweat droplet formation was significantly slower and the sweat droplet size larger and more variable in db/db mice compared to controls. Whereas pilocarpine and glycopyrrolate increased and decreased sweating, respectively, in 6 month-old controls, db/db mice did not respond to pharmacologic manipulations. Our findings indicate autonomic neuropathy is an early and prominent deficit in the db/db model and have implications for the development of therapies for peripheral diabetic neuropathy. Nature Publishing Group 2017-01-27 /pmc/articles/PMC5269750/ /pubmed/28128284 http://dx.doi.org/10.1038/srep41401 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Liu, Ying Sebastian, Blessan Liu, Ben Zhang, Yiyue Fissel, John A. Pan, Baohan Polydefkis, Michael Farah, Mohamed H. Sensory and autonomic function and structure in footpads of a diabetic mouse model |
title | Sensory and autonomic function and structure in footpads of a diabetic mouse model |
title_full | Sensory and autonomic function and structure in footpads of a diabetic mouse model |
title_fullStr | Sensory and autonomic function and structure in footpads of a diabetic mouse model |
title_full_unstemmed | Sensory and autonomic function and structure in footpads of a diabetic mouse model |
title_short | Sensory and autonomic function and structure in footpads of a diabetic mouse model |
title_sort | sensory and autonomic function and structure in footpads of a diabetic mouse model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5269750/ https://www.ncbi.nlm.nih.gov/pubmed/28128284 http://dx.doi.org/10.1038/srep41401 |
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