Participation of hippocampal 5-HT5A, 5-HT6 and 5-HT7 serotonin receptors on the consolidation of social recognition memory

•The blockade of 5-HT5A receptors in the CA1 impairs the consolidation of social recognition memory (SRM).•The activation of 5-HT6 receptors in the CA1 impairs the consolidation of SRM.•The activation of 5-HT7 receptors in the CA1 impairs the consolidation of SRM. Social recognition is the ability o...

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Veröffentlicht in:Neuroscience 2022-08, Vol.497, p.171-183
Hauptverfasser: Schmidt, Scheila Daiane, Zinn, Carolina Garrido, Cavalcante, Lorena Evelyn, Ferreira, Flávia Fagundes, Furini, Cristiane Regina Guerino, Izquierdo, Ivan, de Carvalho Myskiw, Jociane
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Sprache:eng
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Zusammenfassung:•The blockade of 5-HT5A receptors in the CA1 impairs the consolidation of social recognition memory (SRM).•The activation of 5-HT6 receptors in the CA1 impairs the consolidation of SRM.•The activation of 5-HT7 receptors in the CA1 impairs the consolidation of SRM. Social recognition is the ability of animals to identify and recognize a conspecific. The consolidation of social stimuli in long-term memory is crucial for the establishment and maintenance of social groups, reproduction and species survival. Despite its importance, little is known about the circuitry and molecular mechanisms involved in the social recognition memory (SRM). Serotonin (5-hydroxytryptamine, 5-HT) is acknowledged as a major neuromodulator, which plays a key role in learning and memory. Focusing on the more recently described 5-HT receptors, we investigated in the CA1 region of the dorsal hippocampus the participation of 5-HT5A, 5-HT6 and 5-HT7 receptors in the consolidation of social recognition memory (SRM). Male Wistar rats cannulated in CA1 were subjected to a social discrimination task. In the sample phase the animals were exposed to a juvenile conspecific for 1 h. Immediately after, they received different pharmacological treatments. Twenty-four hours later, they were submitted to a 5 min retention test in the presence of the previously presented juvenile (familiar) and a novel juvenile. The animals that received infusions of 5-HT5A receptor antagonist SB-699551 (10 µg/µL), 5-HT6 receptor agonist WAY-208466 (0.63 µg/µL) or 5-HT7 receptor agonist AS-19 (5 µg/µL) intra-CA1 were unable to recognize the familiar juvenile. This effect was blocked by the coinfusion of WAY-208466 plus 5-HT6 receptor antagonist SB-271046 (10 µg/µL) or AS-19 plus 5-HT7 receptor antagonist SB-269970 (5 µg/µL). The present study helps to clarify the neurobiological functions of the 5-HT receptors more recently described and extends our knowledge about mechanisms underlying the SRM.
ISSN:0306-4522
1873-7544
DOI:10.1016/j.neuroscience.2022.06.016