Disclaimer: The information contained herein should NOT be used as a substitute for the advice of an appropriately qualified and licensed physician or other health care provider. The tool is not a substitute for the care provided… (more)
“The locomotor hyperactivation induced by acute cocaine (10 mg/kg) was enhanced by MSX-3 (5-25 ….4 mg/kg), while CGS 21680 (0.2 mg/kg), SCH 23390 (0.25 mg/kg), raclopride (0.2-0.8 mg/kg) or ….1 mg/kg) decreased this effect of cocaine.”
“ResultsUsing the same challenge dose of cocaine in both repeated treatment conditions (i.e. 20 mg/kg), the D2 class antagonists eticlopride and raclopride were less potent in attenuating the locomotor effects of cocaine in sensitized than those in non-sensitized animals.”
“Both SCH23390, a D-1 receptor antagonist, and raclopride , a D-2 antagonist, inhibited all behaviors induced by cocaine , suggesting that the behavioral actions of cocaine may involve the activation of D-1 and D-2 receptors.”
Pharmacology Biochemistry and Behavior • 1991 | View Paper
“The concomitant administration of both D1R and D2R antagonists, SCH 23390 (D1R selective) and raclopride (D2R selective), blocked cocaine induced-behavioral sensitization, CART over-expression, and cyclic adenosine 5'-monophosphate (cAMP)/protein kinase A (PKA)/phospho-cAMP response element-binding protein (pCREB) signal pathways.”
The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology • 2015 | View Paper
Help us improve supp.ai, we'd love to hear your feedback:Submit Feedback