Acetic acid- and phenyl-p-benzoquinone-induced overt pain-like behavior depends on spinal activation of MAP kinases, PI3K and microglia in mice


Autoria(s): Pavao-de-Souza, Gabriela F.; Zarpelon, Ana C.; Tedeschi, Giovana C.; Mizokami, Sandra S.; Sanson, Joice S.; Cunha, Thiago M.; Ferreira, Sergio H.; Cunha, Fernando Q.; Casagrande, Rubia; Verri, Waldiceu A., Jr.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

27/09/2013

27/09/2013

2012

Resumo

The acetic acid and phenyl-p-benzoquinone are easy and fast screening models to access the activity of novel candidates as analgesic drugs and their mechanisms. These models induce a characteristic and quantifiable overt pain-like behavior described as writhing response or abdominal contortions. The knowledge of the mechanisms involved in the chosen model is a crucial step forward demonstrating the mechanisms that the candidate drug would inhibit because the mechanisms triggered in that model will be addressed. Herein, it was investigated the role of spinal mitogen-activated protein (MAP) kinases ERK (extracellular signal-regulated kinase), JNK (Jun N-terminal Kinase) and p38, PI3K (phosphatidylinositol 3-kinase) and microglia in the writhing response induced by acetic acid and phenyl-p-benzoquinone, and flinch induced by formalin in mice. Acetic acid and phenyl-p-benzoquinone induced significant writhing response over 20 min. The nociceptive response in these models were significantly and in a dose-dependent manner reduced by intrathecal pre-treatment with ERK (PD98059), JNK (SB600125), p38 (SB202190) or PI3K (wortmannin) inhibitors. Furthermore, the co-treatment with MAP kinase and PI3K inhibitors, at doses that were ineffective as single treatment, significantly inhibited acetic acid- and phenyl-p-benzoquinone-induced nociception. The treatment with microglia inhibitors minocycline and fluorocitrate also diminished the nociceptive response. Similar results were obtained in the formalin test. Concluding. MAP kinases and PI3K are important spinal signaling kinases in acetic acid and phenyl-p-benzoquinone models of overt pain-like behavior and there is also activation of spinal microglia indicating that it is also important to determine whether drugs tested in these models also modulate such spinal mechanisms. (C) 2012 Elsevier Inc. All rights reserved.

Fundacao Araucaria

Fundacao Araucaria

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)

Coordenadoria de Aperfeicoamento de Pessoal de Nivel Superior (CAPES), Brazil

Coordenadoria de Aperfeicoamento de Pessoal de Nivel Superior (CAPES), Brazil

PIBITI/UEL, Brazil

PIBITI/UEL, Brazil

Identificador

PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, OXFORD, v. 101, n. 3, pp. 320-328, MAY, 2012

0091-3057

http://www.producao.usp.br/handle/BDPI/33785

10.1016/j.pbb.2012.01.018

http://dx.doi.org/10.1016/j.pbb.2012.01.018

Idioma(s)

eng

Publicador

PERGAMON-ELSEVIER SCIENCE LTD

OXFORD

Relação

PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR

Direitos

restrictedAccess

Copyright PERGAMON-ELSEVIER SCIENCE LTD

Palavras-Chave #ERK #JNK #P38 #PI3K #MICROGLIA #PAIN #FORMALIN #ABDOMINAL CONTORTIONS #ACETIC ACID #PHENYL-P-BENZOQUINONE #INFLAMMATION #VISCERAL PAIN #INFLAMMATION-INDUCED HYPERALGESIA #NECROSIS-FACTOR-ALPHA #N-TERMINAL KINASE #NEUROPATHIC PAIN #PROTEIN-KINASE #PHOSPHATIDYLINOSITOL 3-KINASE #MECHANICAL ALLODYNIA #SENSORY NEURONS #NERVE LIGATION #CORD #BEHAVIORAL SCIENCES #NEUROSCIENCES #PHARMACOLOGY & PHARMACY
Tipo

article

original article

publishedVersion