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Journal of Zanjan University of Medical Sciences and Health Services. 2009; 17 (67): 11-21
in Persian | IMEMR | ID: emr-102044

ABSTRACT

JWH133 is known to have cannabinoid-2 [CB2] receptor agonist properties. Celecoxib, a selective cyclooxygenase-2 [COX-2] inhibitor, is also known to have antinociceptive properties. Endocannabinoids produce analgesia possibly through cyclooxygenase [COX] pathway. The aim of the present work was: to study the effect of celecoxib on JWH133 induced antinociception and to compare the effects of two different dose ranges of celecoxib [mg/kg and nano g/kg] on the JWH133 antiniciceptive effect. We have studied the possible interaction of administration of mg/kg [50-200 mg/kg] and Ultra-Low Dose [ULD] [25 and 50 ng/kg] of celecoxib on the antinociceptive effect of intraperitoneal [i.p.] injection of JWH133 using formalin test in mice. JWH133 [0.01, 0.1 and 1 mg/kg] induced antinociceptive effect just in phase I of the formalin test. Celecoxib [50-200 mg/kg] and its ULD [25 and 50 ng/kg] attenuated and potentiated, JWH133 induced antinociception, respectively. It is concluded that JWH-133 induced antinociception is modulated by celecoxib and mg/kg doses of celecoxib showed opposite effects compare to its ultra-low doses


Subject(s)
Animals, Laboratory , Mice , Endocannabinoids , Drug Dosage Calculations , Pain Measurement , Pyrazoles , Sulfonamides
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