SB 277011-A (a DRD3 selective antagonist) significantly reduced cue-induced reinstatement at all the doses tested, whereas there was no significant effect of BP 897 (a DRD3 partial agonist) on cue-induced reinstatement of nicotine-seeking or on nicotine-taking behaviour.
|Animal models||Male, Long–Evans rats|
|Dosages||1, 3 and 10 mg/kg|
|Body Surface Area (m2)||0.007||0.025||0.15||0.05||0.02||0.5|
|Animal A (mg/kg) = Animal B (mg/kg) multiplied by||Animal B Km|
|Animal A Km|
For example, to modify the dose of resveratrol used for a mouse (22.4 mg/kg) to a dose based on the BSA for a rat, multiply 22.4 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for resveratrol of 11.2 mg/kg.
|Solubility||10 mM in DMSO|
The selective dopamine D₃ receptor antagonist SB-277011-A significantly decreases binge-like consumption of ethanol in C57BL/J6 mice.
Rice OV, et al. Synapse. 2015 Jun;69(6):295-8. PMID: 25764479.
Effect of the selective dopamine D3 receptor antagonist SB-277011-A on regional c-Fos-like expression in rat forebrain.
Southam E, et al. Brain Res. 2007 May 29;1149:50-7. PMID: 17382304.
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