5-HT 3 receptor antagonist MDL 72222 attenuates cocaine- and mazindol-, but not methylphenidate-induced neurochemical and behavioral effects in the rat

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Molecular geometry of inhibitors of the uptake of catecholamines and serotonin in synaptosomal preparations of rat brain.

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5-HT3 receptors control dopamine release in the nucleus accumbens of freely moving rats

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Effect of the 5-HT3 receptor antagonists, MDL72222 and ondansetron on morphine place conditioning

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GR38032F, a serotonin 5-HT3 antagonist, fails to alter cocaine self-administration in rats

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Failure of ondansetron to block the discriminative or reinforcing stimulus effects of cocaine in the rat

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Local 5HT3 receptors mediate fluoxetine but not desipramine-induced increase of extracellular dopamine in the prefrontal cortex

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MDL72222, a serotonin 5-HT3 receptor antagonist, blocks MDMA's ability to establish a conditioned place preference

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Interactions between 5-HT3 receptors and cerebral dopamine function: implications for the treatment of schizophrenia and psychoactive substance abuse

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Serotonin 5-HT3 antagonists do not alter the discriminative stimulus properties of cocaine

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Cocaine Is Self‐administered into the Shell Region of the Nucleus Accumbens in Wistar Rats

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5‐HT₃ Receptor Antagonist MDL 72222 Dose‐Dependently Attenuates Cocaine‐ and Amphetamine‐Induced Elevations of Extracellular Dopamine in the Nucleus Accumbens and the Dorsal Striatum

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Oxalic acid stabilizes dopamine, serotonin, and their metabolites in automated liquid chromatography with electrochemical detection

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Effects of Methylphenidate Analogues on Phenethylamine Substrates for the Striatal Dopamine Transporter

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Studies on the capacity of mazindol and dita to act as uptake inhibitors or releasing agents for 3H-biogenic amines in rat brain tissue slices

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5-HT3 receptor antagonists do not modify cocaine place conditioning or the rise in extracellular dopamine in the nucleus accumbens of rats

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Different Effects of Tropisetron and Ondansetron in Learning and Memory Paradigms

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Ondansetron fails to attenuate a scopolamineinduced deficit in a Stone maze task

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