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n5-STZ Diabetic Model Develops Alterations in Sciatic Nerve and Dorsal Root Ganglia Neurons of Wistar Rats

One experimental model of diabetes mellitus (DM) similar to type II DM, called n5-STZ, is obtained by a single injection (via i.p.) of streptozotocin (STZ) in the 5th day of life of newborn rats. The present investigation aimed to characterize alterations in excitability of rat peripheral neurons in...

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Autores principales: Ferreira-da-Silva, Francisco Walber, da Silva-Alves, Kerly Shamyra, Lemos-dos-Santos, Matheus, de Oliveira, Keciany Alves, Joca, Humberto Cavalcante, do Vale, Otoni Cardoso, Coelho-de-Souza, Andrelina Noronha, Leal-Cardoso, José Henrique
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3588209/
https://www.ncbi.nlm.nih.gov/pubmed/23476801
http://dx.doi.org/10.1155/2013/638028
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author Ferreira-da-Silva, Francisco Walber
da Silva-Alves, Kerly Shamyra
Lemos-dos-Santos, Matheus
de Oliveira, Keciany Alves
Joca, Humberto Cavalcante
do Vale, Otoni Cardoso
Coelho-de-Souza, Andrelina Noronha
Leal-Cardoso, José Henrique
author_facet Ferreira-da-Silva, Francisco Walber
da Silva-Alves, Kerly Shamyra
Lemos-dos-Santos, Matheus
de Oliveira, Keciany Alves
Joca, Humberto Cavalcante
do Vale, Otoni Cardoso
Coelho-de-Souza, Andrelina Noronha
Leal-Cardoso, José Henrique
author_sort Ferreira-da-Silva, Francisco Walber
collection PubMed
description One experimental model of diabetes mellitus (DM) similar to type II DM, called n5-STZ, is obtained by a single injection (via i.p.) of streptozotocin (STZ) in the 5th day of life of newborn rats. The present investigation aimed to characterize alterations in excitability of rat peripheral neurons in n5-STZ model. n5-STZ DM was induced, and electrophysiological evaluation was done at 12th week of rat life. Rats developed glucose intolerance, sensory alteration, and hyperglycemia or near-normoglycemia (21.2 ± 1.6 and 7.4 ± 0.4 mmol/L). In near-normoglycemia group the significant electrophysiological alteration observed was decreased in amplitude of 2nd wave (2nd component, conduction velocity: 48.8 m/s) of compound action potential (CAP) of sciatic nerve. For hyperglycemic rats, decreased excitability, amplitude, and conduction velocity of 2nd CAP component of sciatic nerve were found; a depolarization of resting potential (4-5 mV) and reduction in maximum ascendant and descendant inclinations of action potential were found in DRG neurons but no alteration on Na(+) current (I(Na(+))). Thus, n5-STZ rats develop alterations in excitability which were related to glycemic levels but were not likely attributable to changes on I(Na(+)). Our data confirm that n5-STZ model is a useful model to study type II DM.
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spelling pubmed-35882092013-03-09 n5-STZ Diabetic Model Develops Alterations in Sciatic Nerve and Dorsal Root Ganglia Neurons of Wistar Rats Ferreira-da-Silva, Francisco Walber da Silva-Alves, Kerly Shamyra Lemos-dos-Santos, Matheus de Oliveira, Keciany Alves Joca, Humberto Cavalcante do Vale, Otoni Cardoso Coelho-de-Souza, Andrelina Noronha Leal-Cardoso, José Henrique ISRN Endocrinol Research Article One experimental model of diabetes mellitus (DM) similar to type II DM, called n5-STZ, is obtained by a single injection (via i.p.) of streptozotocin (STZ) in the 5th day of life of newborn rats. The present investigation aimed to characterize alterations in excitability of rat peripheral neurons in n5-STZ model. n5-STZ DM was induced, and electrophysiological evaluation was done at 12th week of rat life. Rats developed glucose intolerance, sensory alteration, and hyperglycemia or near-normoglycemia (21.2 ± 1.6 and 7.4 ± 0.4 mmol/L). In near-normoglycemia group the significant electrophysiological alteration observed was decreased in amplitude of 2nd wave (2nd component, conduction velocity: 48.8 m/s) of compound action potential (CAP) of sciatic nerve. For hyperglycemic rats, decreased excitability, amplitude, and conduction velocity of 2nd CAP component of sciatic nerve were found; a depolarization of resting potential (4-5 mV) and reduction in maximum ascendant and descendant inclinations of action potential were found in DRG neurons but no alteration on Na(+) current (I(Na(+))). Thus, n5-STZ rats develop alterations in excitability which were related to glycemic levels but were not likely attributable to changes on I(Na(+)). Our data confirm that n5-STZ model is a useful model to study type II DM. Hindawi Publishing Corporation 2013-02-17 /pmc/articles/PMC3588209/ /pubmed/23476801 http://dx.doi.org/10.1155/2013/638028 Text en Copyright © 2013 Francisco Walber Ferreira-da-Silva et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Ferreira-da-Silva, Francisco Walber
da Silva-Alves, Kerly Shamyra
Lemos-dos-Santos, Matheus
de Oliveira, Keciany Alves
Joca, Humberto Cavalcante
do Vale, Otoni Cardoso
Coelho-de-Souza, Andrelina Noronha
Leal-Cardoso, José Henrique
n5-STZ Diabetic Model Develops Alterations in Sciatic Nerve and Dorsal Root Ganglia Neurons of Wistar Rats
title n5-STZ Diabetic Model Develops Alterations in Sciatic Nerve and Dorsal Root Ganglia Neurons of Wistar Rats
title_full n5-STZ Diabetic Model Develops Alterations in Sciatic Nerve and Dorsal Root Ganglia Neurons of Wistar Rats
title_fullStr n5-STZ Diabetic Model Develops Alterations in Sciatic Nerve and Dorsal Root Ganglia Neurons of Wistar Rats
title_full_unstemmed n5-STZ Diabetic Model Develops Alterations in Sciatic Nerve and Dorsal Root Ganglia Neurons of Wistar Rats
title_short n5-STZ Diabetic Model Develops Alterations in Sciatic Nerve and Dorsal Root Ganglia Neurons of Wistar Rats
title_sort n5-stz diabetic model develops alterations in sciatic nerve and dorsal root ganglia neurons of wistar rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3588209/
https://www.ncbi.nlm.nih.gov/pubmed/23476801
http://dx.doi.org/10.1155/2013/638028
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