Reversal of a cholinergic-induced deficit in a rodent model of recognition memory by the selective 5-HT6 receptor antagonist, Ro 04-6790

• Published in: Psychopharmacologia Vol. 170; no. 4; pp. 358 - 367
• Main Authors: WOOLLEY, Marie L, MARSDEN, Charles A, SLEIGHT, Andrew J, FONE, Kevin C. F
• Format: Journal Article
• Language: English
• Published: Berlin Springer 01.12.2003; Springer Nature B.V
• Subjects: Animals; Behavior, Animal - drug effects; Biological and medical sciences; Cognitive ability; Dopamine Antagonists - pharmacology; Dose-Response Relationship, Drug; Drug Interactions; Hydrocarbons; Male; Medical sciences; Memory; Memory - drug effects; Miscellaneous; Muscarinic Antagonists - pharmacology; Neuropharmacology; Pharmacology. Drug treatments; Pyrimidines - pharmacology; Raclopride - antagonists & inhibitors; Rats; Rodents; Scopolamine Hydrobromide - antagonists & inhibitors; Serotonin Antagonists - pharmacology; Recognition memory; Intraperitoneal administration; Rat; Memory; Rodentia; 5-HT6 serotonin receptor; Cognition; Biological activity; Vertebrata; Mammalia; Animal; Antagonist; Mechanism of action; Cholinergic transmission
• ISSN: 0033-3158; 1432-2072
• DOI: 10.1007/s00213-003-1552-5

Accumulating evidence suggests a potential role for the 5-HT(6 )receptor in cognitive function and the potential use of 5-HT(6) receptor antagonists in the treatment of learning and memory disorders. The aim of the current study was to investigate the effect of the selective 5-HT(6) receptor antagonist, Ro 04-6790, on both the performance of normal adult rats and restoration of a pharmacological disruption of memory function produced by the non-selective muscarinic receptor antagonist, scopolamine, or the dopamine D(2) receptor antagonist, raclopride, in a rodent model of recognition memory. Passive, perceptually based, recognition memory was assessed using a novel object discrimination task. Following habituation to an arena, rats were presented with two identical objects during trial 1 (T(1)) and a novel and familiar object during trial 2 (T(2)). The time spent exploring the two objects in each trial was measured and novel object discrimination assessed in T(2). In the absence of drug all rats spent an equal time exploring the two identical objects in T(1) but more time exploring the novel object in T(2). Scopolamine (but not N-methylscopolamine) and raclopride both produced a dose-dependent reduction in novel object discrimination whilst the 5-HT(6) receptor antagonist, Ro 04-6790, had no effect on discrimination when given alone but completely reversed the scopolamine- but not the raclopride-induced deficit. This study demonstrates that acute administration of Ro 04-6790 reverses a cholinergic but not a dopaminergic deficit in a rodent model of recognition memory and provides further support for a role of the 5-HT(6) receptor in the regulation of cognitive function.