Participation of neuronal nitric oxide synthase in experimental neuropathic pain induced by sciatic nerve transection

Nerve injury leads to a neuropathic pain state that results from central sensitization. This phenomenom is mediated by NMDA receptors and may involve the production of nitric oxide (NO). In this study, we investigated the expression of the neuronal isoform of NO synthase (nNOS) in the spinal cord of...

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Main Authors: M. Chacur, R.J.B. Matos, A.S. Alves, A.C. Rodrigues, V. Gutierrez, Y. Cury, L.R.G. Britto
Format: Article
Language:English
Published: Associação Brasileira de Divulgação Científica 2010-04-01
Series:Brazilian Journal of Medical and Biological Research
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2010000400008
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author M. Chacur
R.J.B. Matos
A.S. Alves
A.C. Rodrigues
V. Gutierrez
Y. Cury
L.R.G. Britto
author_facet M. Chacur
R.J.B. Matos
A.S. Alves
A.C. Rodrigues
V. Gutierrez
Y. Cury
L.R.G. Britto
author_sort M. Chacur
collection DOAJ
description Nerve injury leads to a neuropathic pain state that results from central sensitization. This phenomenom is mediated by NMDA receptors and may involve the production of nitric oxide (NO). In this study, we investigated the expression of the neuronal isoform of NO synthase (nNOS) in the spinal cord of 3-month-old male, Wistar rats after sciatic nerve transection (SNT). Our attention was focused on the dorsal part of L3-L5 segments receiving sensory inputs from the sciatic nerve. SNT resulted in the development of neuropathic pain symptoms confirmed by evaluating mechanical hyperalgesia (Randall and Selitto test) and allodynia (von Frey hair test). Control animals did not present any alteration (sham-animals). The selective inhibitor of nNOS, 7-nitroindazole (0.2 and 2 µg in 50 µL), blocked hyperalgesia and allodynia induced by SNT. Immunohistochemical analysis showed that nNOS was increased (48% by day 30) in the lumbar spinal cord after SNT. This increase was observed near the central canal (Rexed’s lamina X) and also in lamina I-IV of the dorsal horn. Real-time PCR results indicated an increase of nNOS mRNA detected from 1 to 30 days after SNT, with the highest increase observed 1 day after injury (1469%). Immunoblotting confirmed the increase of nNOS in the spinal cord between 1 and 15 days post-lesion (20%), reaching the greatest increase (60%) 30 days after surgery. The present findings demonstrate an increase of nNOS after peripheral nerve injury that may contribute to the increase of NO production observed after peripheral neuropathy.
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spelling doaj.art-04a4d212676a40d9aad5d4910b0132882022-12-21T17:15:39ZengAssociação Brasileira de Divulgação CientíficaBrazilian Journal of Medical and Biological Research0100-879X1414-431X2010-04-01434367376Participation of neuronal nitric oxide synthase in experimental neuropathic pain induced by sciatic nerve transectionM. ChacurR.J.B. MatosA.S. AlvesA.C. RodriguesV. GutierrezY. CuryL.R.G. BrittoNerve injury leads to a neuropathic pain state that results from central sensitization. This phenomenom is mediated by NMDA receptors and may involve the production of nitric oxide (NO). In this study, we investigated the expression of the neuronal isoform of NO synthase (nNOS) in the spinal cord of 3-month-old male, Wistar rats after sciatic nerve transection (SNT). Our attention was focused on the dorsal part of L3-L5 segments receiving sensory inputs from the sciatic nerve. SNT resulted in the development of neuropathic pain symptoms confirmed by evaluating mechanical hyperalgesia (Randall and Selitto test) and allodynia (von Frey hair test). Control animals did not present any alteration (sham-animals). The selective inhibitor of nNOS, 7-nitroindazole (0.2 and 2 µg in 50 µL), blocked hyperalgesia and allodynia induced by SNT. Immunohistochemical analysis showed that nNOS was increased (48% by day 30) in the lumbar spinal cord after SNT. This increase was observed near the central canal (Rexed’s lamina X) and also in lamina I-IV of the dorsal horn. Real-time PCR results indicated an increase of nNOS mRNA detected from 1 to 30 days after SNT, with the highest increase observed 1 day after injury (1469%). Immunoblotting confirmed the increase of nNOS in the spinal cord between 1 and 15 days post-lesion (20%), reaching the greatest increase (60%) 30 days after surgery. The present findings demonstrate an increase of nNOS after peripheral nerve injury that may contribute to the increase of NO production observed after peripheral neuropathy.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2010000400008AllodyniaNeuropathic painNeuronal nitric oxide synthasePeripheral neuropathySciatic nerve transectionSpinal cord
spellingShingle M. Chacur
R.J.B. Matos
A.S. Alves
A.C. Rodrigues
V. Gutierrez
Y. Cury
L.R.G. Britto
Participation of neuronal nitric oxide synthase in experimental neuropathic pain induced by sciatic nerve transection
Brazilian Journal of Medical and Biological Research
Allodynia
Neuropathic pain
Neuronal nitric oxide synthase
Peripheral neuropathy
Sciatic nerve transection
Spinal cord
title Participation of neuronal nitric oxide synthase in experimental neuropathic pain induced by sciatic nerve transection
title_full Participation of neuronal nitric oxide synthase in experimental neuropathic pain induced by sciatic nerve transection
title_fullStr Participation of neuronal nitric oxide synthase in experimental neuropathic pain induced by sciatic nerve transection
title_full_unstemmed Participation of neuronal nitric oxide synthase in experimental neuropathic pain induced by sciatic nerve transection
title_short Participation of neuronal nitric oxide synthase in experimental neuropathic pain induced by sciatic nerve transection
title_sort participation of neuronal nitric oxide synthase in experimental neuropathic pain induced by sciatic nerve transection
topic Allodynia
Neuropathic pain
Neuronal nitric oxide synthase
Peripheral neuropathy
Sciatic nerve transection
Spinal cord
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2010000400008
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