The superoxide anion donor, potassium superoxide, induces pain and inflammation in mice through production of reactive oxygen species and cyclooxygenase-2
It is currently accepted that superoxide anion (O2•−) is an important mediator in pain and inflammation. The role of superoxide anion in pain and inflammation has been mainly determined indirectly by modulating its production and inactivation. Direct evidence using potassium superoxide (KO2), a superoxide anion donor, demonstrated that it induced thermal hyperalgesia, as assessed by the Hargreaves method. However, it remains to be determined whether KO2 is capable of inducing other inflammatory and nociceptive responses attributed to superoxide anion. Therefore, in the present study, we investigated the nociceptive and inflammatory effects of KO2. The KO2-induced inflammatory responses evaluated in mice were: mechanical hyperalgesia (electronic version of von Frey filaments), thermal hyperalgesia (hot plate), edema (caliper rule), myeloperoxidase activity (colorimetric assay), overt pain-like behaviors (flinches, time spent licking and writhing score), leukocyte recruitment, oxidative stress, and cyclooxygenase-2 mRNA expression (quantitative PCR). Administration of KO2 induced mechanical hyperalgesia, thermal hyperalgesia, paw edema, leukocyte recruitment, the writhing response, paw flinching, and paw licking in a dose-dependent manner. KO2 also induced time-dependent cyclooxygenase-2 mRNA expression in the paw skin. The nociceptive, inflammatory, and oxidative stress components of KO2-induced responses were responsive to morphine (analgesic opioid), quercetin (antioxidant flavonoid), and/or celecoxib (anti-inflammatory cyclooxygenase-2 inhibitor) treatment. In conclusion, the well-established superoxide anion donor KO2 is a valuable tool for studying the mechanisms and pharmacological susceptibilities of superoxide anion-triggered nociceptive and inflammatory responses ranging from mechanical and thermal hyperalgesia to overt pain-like behaviors, edema, and leukocyte recruitment.
Main Authors: | , , , , , , , , , , , |
---|---|
Format: | Digital revista |
Language: | English |
Published: |
Associação Brasileira de Divulgação Científica
2015
|
Online Access: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2015000400321 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
id |
oai:scielo:S0100-879X2015000400321 |
---|---|
record_format |
ojs |
spelling |
oai:scielo:S0100-879X20150004003212019-03-19The superoxide anion donor, potassium superoxide, induces pain and inflammation in mice through production of reactive oxygen species and cyclooxygenase-2Maioli,N.A.Zarpelon,A.C.Mizokami,S.S.Calixto-Campos,C.Guazelli,C.F.S.Hohmann,M.S.N.Pinho-Ribeiro,F.A.Carvalho,T.T.Manchope,M.F.Ferraz,C.R.Casagrande,R.Verri Jr,W.A. Superoxide anion Potassium superoxide Pain Inflammation Oxidative stress It is currently accepted that superoxide anion (O2•−) is an important mediator in pain and inflammation. The role of superoxide anion in pain and inflammation has been mainly determined indirectly by modulating its production and inactivation. Direct evidence using potassium superoxide (KO2), a superoxide anion donor, demonstrated that it induced thermal hyperalgesia, as assessed by the Hargreaves method. However, it remains to be determined whether KO2 is capable of inducing other inflammatory and nociceptive responses attributed to superoxide anion. Therefore, in the present study, we investigated the nociceptive and inflammatory effects of KO2. The KO2-induced inflammatory responses evaluated in mice were: mechanical hyperalgesia (electronic version of von Frey filaments), thermal hyperalgesia (hot plate), edema (caliper rule), myeloperoxidase activity (colorimetric assay), overt pain-like behaviors (flinches, time spent licking and writhing score), leukocyte recruitment, oxidative stress, and cyclooxygenase-2 mRNA expression (quantitative PCR). Administration of KO2 induced mechanical hyperalgesia, thermal hyperalgesia, paw edema, leukocyte recruitment, the writhing response, paw flinching, and paw licking in a dose-dependent manner. KO2 also induced time-dependent cyclooxygenase-2 mRNA expression in the paw skin. The nociceptive, inflammatory, and oxidative stress components of KO2-induced responses were responsive to morphine (analgesic opioid), quercetin (antioxidant flavonoid), and/or celecoxib (anti-inflammatory cyclooxygenase-2 inhibitor) treatment. In conclusion, the well-established superoxide anion donor KO2 is a valuable tool for studying the mechanisms and pharmacological susceptibilities of superoxide anion-triggered nociceptive and inflammatory responses ranging from mechanical and thermal hyperalgesia to overt pain-like behaviors, edema, and leukocyte recruitment.info:eu-repo/semantics/openAccessAssociação Brasileira de Divulgação CientíficaBrazilian Journal of Medical and Biological Research v.48 n.4 20152015-04-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2015000400321en10.1590/1414-431x20144187 |
institution |
SCIELO |
collection |
OJS |
country |
Brasil |
countrycode |
BR |
component |
Revista |
access |
En linea |
databasecode |
rev-scielo-br |
tag |
revista |
region |
America del Sur |
libraryname |
SciELO |
language |
English |
format |
Digital |
author |
Maioli,N.A. Zarpelon,A.C. Mizokami,S.S. Calixto-Campos,C. Guazelli,C.F.S. Hohmann,M.S.N. Pinho-Ribeiro,F.A. Carvalho,T.T. Manchope,M.F. Ferraz,C.R. Casagrande,R. Verri Jr,W.A. |
spellingShingle |
Maioli,N.A. Zarpelon,A.C. Mizokami,S.S. Calixto-Campos,C. Guazelli,C.F.S. Hohmann,M.S.N. Pinho-Ribeiro,F.A. Carvalho,T.T. Manchope,M.F. Ferraz,C.R. Casagrande,R. Verri Jr,W.A. The superoxide anion donor, potassium superoxide, induces pain and inflammation in mice through production of reactive oxygen species and cyclooxygenase-2 |
author_facet |
Maioli,N.A. Zarpelon,A.C. Mizokami,S.S. Calixto-Campos,C. Guazelli,C.F.S. Hohmann,M.S.N. Pinho-Ribeiro,F.A. Carvalho,T.T. Manchope,M.F. Ferraz,C.R. Casagrande,R. Verri Jr,W.A. |
author_sort |
Maioli,N.A. |
title |
The superoxide anion donor, potassium superoxide, induces pain and inflammation in mice through production of reactive oxygen species and cyclooxygenase-2 |
title_short |
The superoxide anion donor, potassium superoxide, induces pain and inflammation in mice through production of reactive oxygen species and cyclooxygenase-2 |
title_full |
The superoxide anion donor, potassium superoxide, induces pain and inflammation in mice through production of reactive oxygen species and cyclooxygenase-2 |
title_fullStr |
The superoxide anion donor, potassium superoxide, induces pain and inflammation in mice through production of reactive oxygen species and cyclooxygenase-2 |
title_full_unstemmed |
The superoxide anion donor, potassium superoxide, induces pain and inflammation in mice through production of reactive oxygen species and cyclooxygenase-2 |
title_sort |
superoxide anion donor, potassium superoxide, induces pain and inflammation in mice through production of reactive oxygen species and cyclooxygenase-2 |
description |
It is currently accepted that superoxide anion (O2•−) is an important mediator in pain and inflammation. The role of superoxide anion in pain and inflammation has been mainly determined indirectly by modulating its production and inactivation. Direct evidence using potassium superoxide (KO2), a superoxide anion donor, demonstrated that it induced thermal hyperalgesia, as assessed by the Hargreaves method. However, it remains to be determined whether KO2 is capable of inducing other inflammatory and nociceptive responses attributed to superoxide anion. Therefore, in the present study, we investigated the nociceptive and inflammatory effects of KO2. The KO2-induced inflammatory responses evaluated in mice were: mechanical hyperalgesia (electronic version of von Frey filaments), thermal hyperalgesia (hot plate), edema (caliper rule), myeloperoxidase activity (colorimetric assay), overt pain-like behaviors (flinches, time spent licking and writhing score), leukocyte recruitment, oxidative stress, and cyclooxygenase-2 mRNA expression (quantitative PCR). Administration of KO2 induced mechanical hyperalgesia, thermal hyperalgesia, paw edema, leukocyte recruitment, the writhing response, paw flinching, and paw licking in a dose-dependent manner. KO2 also induced time-dependent cyclooxygenase-2 mRNA expression in the paw skin. The nociceptive, inflammatory, and oxidative stress components of KO2-induced responses were responsive to morphine (analgesic opioid), quercetin (antioxidant flavonoid), and/or celecoxib (anti-inflammatory cyclooxygenase-2 inhibitor) treatment. In conclusion, the well-established superoxide anion donor KO2 is a valuable tool for studying the mechanisms and pharmacological susceptibilities of superoxide anion-triggered nociceptive and inflammatory responses ranging from mechanical and thermal hyperalgesia to overt pain-like behaviors, edema, and leukocyte recruitment. |
publisher |
Associação Brasileira de Divulgação Científica |
publishDate |
2015 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2015000400321 |
work_keys_str_mv |
AT maiolina thesuperoxideaniondonorpotassiumsuperoxideinducespainandinflammationinmicethroughproductionofreactiveoxygenspeciesandcyclooxygenase2 AT zarpelonac thesuperoxideaniondonorpotassiumsuperoxideinducespainandinflammationinmicethroughproductionofreactiveoxygenspeciesandcyclooxygenase2 AT mizokamiss thesuperoxideaniondonorpotassiumsuperoxideinducespainandinflammationinmicethroughproductionofreactiveoxygenspeciesandcyclooxygenase2 AT calixtocamposc thesuperoxideaniondonorpotassiumsuperoxideinducespainandinflammationinmicethroughproductionofreactiveoxygenspeciesandcyclooxygenase2 AT guazellicfs thesuperoxideaniondonorpotassiumsuperoxideinducespainandinflammationinmicethroughproductionofreactiveoxygenspeciesandcyclooxygenase2 AT hohmannmsn thesuperoxideaniondonorpotassiumsuperoxideinducespainandinflammationinmicethroughproductionofreactiveoxygenspeciesandcyclooxygenase2 AT pinhoribeirofa thesuperoxideaniondonorpotassiumsuperoxideinducespainandinflammationinmicethroughproductionofreactiveoxygenspeciesandcyclooxygenase2 AT carvalhott thesuperoxideaniondonorpotassiumsuperoxideinducespainandinflammationinmicethroughproductionofreactiveoxygenspeciesandcyclooxygenase2 AT manchopemf thesuperoxideaniondonorpotassiumsuperoxideinducespainandinflammationinmicethroughproductionofreactiveoxygenspeciesandcyclooxygenase2 AT ferrazcr thesuperoxideaniondonorpotassiumsuperoxideinducespainandinflammationinmicethroughproductionofreactiveoxygenspeciesandcyclooxygenase2 AT casagrander thesuperoxideaniondonorpotassiumsuperoxideinducespainandinflammationinmicethroughproductionofreactiveoxygenspeciesandcyclooxygenase2 AT verrijrwa thesuperoxideaniondonorpotassiumsuperoxideinducespainandinflammationinmicethroughproductionofreactiveoxygenspeciesandcyclooxygenase2 AT maiolina superoxideaniondonorpotassiumsuperoxideinducespainandinflammationinmicethroughproductionofreactiveoxygenspeciesandcyclooxygenase2 AT zarpelonac superoxideaniondonorpotassiumsuperoxideinducespainandinflammationinmicethroughproductionofreactiveoxygenspeciesandcyclooxygenase2 AT mizokamiss superoxideaniondonorpotassiumsuperoxideinducespainandinflammationinmicethroughproductionofreactiveoxygenspeciesandcyclooxygenase2 AT calixtocamposc superoxideaniondonorpotassiumsuperoxideinducespainandinflammationinmicethroughproductionofreactiveoxygenspeciesandcyclooxygenase2 AT guazellicfs superoxideaniondonorpotassiumsuperoxideinducespainandinflammationinmicethroughproductionofreactiveoxygenspeciesandcyclooxygenase2 AT hohmannmsn superoxideaniondonorpotassiumsuperoxideinducespainandinflammationinmicethroughproductionofreactiveoxygenspeciesandcyclooxygenase2 AT pinhoribeirofa superoxideaniondonorpotassiumsuperoxideinducespainandinflammationinmicethroughproductionofreactiveoxygenspeciesandcyclooxygenase2 AT carvalhott superoxideaniondonorpotassiumsuperoxideinducespainandinflammationinmicethroughproductionofreactiveoxygenspeciesandcyclooxygenase2 AT manchopemf superoxideaniondonorpotassiumsuperoxideinducespainandinflammationinmicethroughproductionofreactiveoxygenspeciesandcyclooxygenase2 AT ferrazcr superoxideaniondonorpotassiumsuperoxideinducespainandinflammationinmicethroughproductionofreactiveoxygenspeciesandcyclooxygenase2 AT casagrander superoxideaniondonorpotassiumsuperoxideinducespainandinflammationinmicethroughproductionofreactiveoxygenspeciesandcyclooxygenase2 AT verrijrwa superoxideaniondonorpotassiumsuperoxideinducespainandinflammationinmicethroughproductionofreactiveoxygenspeciesandcyclooxygenase2 |
_version_ |
1756391497697067008 |