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Physiol Behav ; 138: 273-8, 2015 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-25447472

RESUMO

The interaction between antinociception induced by CB1 agonist and muscarinic receptor modulators has not been studied yet. In the present study, the effect of pilocarpine (a muscarinic agonist) and atropine (a muscarinic antagonist) on arachidonylcyclopropylamide (ACPA, a CB1 agonist) induced antinociception was studied in mice. In this study the antinociceptive effect of intracerebroventricular administration of ACPA (0.001-2 µg/mice) or intraperitoneal injection of pilocarpine (2.5-20mg/kg) or atropine (1 and 5mg/kg) were studied individually. Then the effect of co-administration of pilocarine (2.5mg/kg) or atropine (5mg/kg) and ACPA (0.001-2 µg/mice) were studied as well. ACPA and pilocarpine induced antinociception in mice but atropine did not. Pilocarpine potentiated but atropine antagonized the antinociceptive effect of ACPA. It is concluded that ACPA induced antinociception is influenced by muscarinic receptor modulators in mice.


Assuntos
Analgésicos não Narcóticos/farmacologia , Ácidos Araquidônicos/farmacologia , Agonistas Muscarínicos/farmacologia , Antagonistas Muscarínicos/farmacologia , Dor Nociceptiva/tratamento farmacológico , Animais , Atropina/farmacologia , Agonistas de Receptores de Canabinoides/farmacologia , Cateteres de Demora , Formaldeído/toxicidade , Injeções Intraventriculares , Masculino , Camundongos , Atividade Motora/efeitos dos fármacos , Dor Nociceptiva/induzido quimicamente , Dor Nociceptiva/fisiopatologia , Medição da Dor , Pilocarpina/farmacologia , Receptor CB1 de Canabinoide/agonistas , Receptor CB1 de Canabinoide/metabolismo
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