Intrinsic activity estimation of cannabinoid CB1 receptor ligands in a drug discrimination paradigm

The present study estimated the apparent intrinsic activity of the cannabinoid CB1 receptor ligands CP 55,940, Δ-tetrahydrocannabinol (Δ-THC) and SR 141716A in a highly sensitive in vivo assay. Rats were trained to discriminate the cannabinoid CB1 receptor agonist CP 55,940 (either 0.03 or 0.014 mg/...

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Veröffentlicht in:Behavioural pharmacology 2003-09, Vol.14 (56), p.471-476
Hauptverfasser: De Vry, J, Jentzsch, K. R
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description The present study estimated the apparent intrinsic activity of the cannabinoid CB1 receptor ligands CP 55,940, Δ-tetrahydrocannabinol (Δ-THC) and SR 141716A in a highly sensitive in vivo assay. Rats were trained to discriminate the cannabinoid CB1 receptor agonist CP 55,940 (either 0.03 or 0.014 mg/kg, i.p., t=30 min) from vehicle, in a two-lever food-reinforced procedure, and were subsequently tested with the three compounds. Although reduction of the training dose did not affect the maximum level of generalization or antagonism (>80% generalization for CP 55,940 and Δ-THC; 0% generalization and >80% antagonism for SR 141716A), the potency of the compounds was differentially affected. Thus, the generalization curves obtained with CP 55,940 and Δ-THC were shifted three- and sixfold to the left; whereas no potency difference was obtained for the antagonism of CP 55,940 by SR 141716A. The data are consistent with the hypothesis that the level of intrinsic activity of CP 55,940 is higher than that of Δ-THC, and that SR 141716A may have a very low level of intrinsic activity. It is concluded that variation of the training dose increases the sensitivity of the in vivo intrinsic activity estimation of cannabinoid CB1 receptor ligands.
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R</creatorcontrib><description>The present study estimated the apparent intrinsic activity of the cannabinoid CB1 receptor ligands CP 55,940, Δ-tetrahydrocannabinol (Δ-THC) and SR 141716A in a highly sensitive in vivo assay. Rats were trained to discriminate the cannabinoid CB1 receptor agonist CP 55,940 (either 0.03 or 0.014 mg/kg, i.p., t=30 min) from vehicle, in a two-lever food-reinforced procedure, and were subsequently tested with the three compounds. Although reduction of the training dose did not affect the maximum level of generalization or antagonism (&gt;80% generalization for CP 55,940 and Δ-THC; 0% generalization and &gt;80% antagonism for SR 141716A), the potency of the compounds was differentially affected. Thus, the generalization curves obtained with CP 55,940 and Δ-THC were shifted three- and sixfold to the left; whereas no potency difference was obtained for the antagonism of CP 55,940 by SR 141716A. The data are consistent with the hypothesis that the level of intrinsic activity of CP 55,940 is higher than that of Δ-THC, and that SR 141716A may have a very low level of intrinsic activity. 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R</creatorcontrib><title>Intrinsic activity estimation of cannabinoid CB1 receptor ligands in a drug discrimination paradigm</title><title>Behavioural pharmacology</title><description>The present study estimated the apparent intrinsic activity of the cannabinoid CB1 receptor ligands CP 55,940, Δ-tetrahydrocannabinol (Δ-THC) and SR 141716A in a highly sensitive in vivo assay. Rats were trained to discriminate the cannabinoid CB1 receptor agonist CP 55,940 (either 0.03 or 0.014 mg/kg, i.p., t=30 min) from vehicle, in a two-lever food-reinforced procedure, and were subsequently tested with the three compounds. Although reduction of the training dose did not affect the maximum level of generalization or antagonism (&gt;80% generalization for CP 55,940 and Δ-THC; 0% generalization and &gt;80% antagonism for SR 141716A), the potency of the compounds was differentially affected. Thus, the generalization curves obtained with CP 55,940 and Δ-THC were shifted three- and sixfold to the left; whereas no potency difference was obtained for the antagonism of CP 55,940 by SR 141716A. The data are consistent with the hypothesis that the level of intrinsic activity of CP 55,940 is higher than that of Δ-THC, and that SR 141716A may have a very low level of intrinsic activity. 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Although reduction of the training dose did not affect the maximum level of generalization or antagonism (&gt;80% generalization for CP 55,940 and Δ-THC; 0% generalization and &gt;80% antagonism for SR 141716A), the potency of the compounds was differentially affected. Thus, the generalization curves obtained with CP 55,940 and Δ-THC were shifted three- and sixfold to the left; whereas no potency difference was obtained for the antagonism of CP 55,940 by SR 141716A. The data are consistent with the hypothesis that the level of intrinsic activity of CP 55,940 is higher than that of Δ-THC, and that SR 141716A may have a very low level of intrinsic activity. It is concluded that variation of the training dose increases the sensitivity of the in vivo intrinsic activity estimation of cannabinoid CB1 receptor ligands.</abstract><pub>Lippincott Williams &amp; Wilkins, Inc</pub></addata></record>
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