ArticleSystemic injection of p-chloroamphetamine eliminates the effect of the 5-HT3 compounds on learning☆
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Synergistic effect between prelimbic 5-HT3 and CB1 receptors on memory consolidation deficit in adult male Sprague-Dawley rats: An isobologram analysis
2016, NeuroscienceCitation Excerpt :Performance of 5-HTRs in various tasks could either be facilitating or disruptive (Roman and Marchetti, 1998; Meneses and Perez-Garcia, 2007). Our data are in agreement with the reports indicating that IP injection of m-CPBG, induced aversive learning deficit in the passive avoidance task (Rajan et al., 2011), also dose-dependently impaired short- and long-term memory in the autoshaping task (Meneses, 2007) and decreased the retention of the conditioned response (CR), in an associative learning task (Hong and Meneses, 1996). It was also reported that intra-CA3 injection of m-CPBG impaired aversive memory acquisition in a one-trial passive avoidance task (Nasehi et al., 2015a).
Neurotransmitters and Memory: Cholinergic, Glutamatergic, GaBAergic, Dopaminergic, Serotonergic, Signaling, and Memory
2013, Identification of Neural Markers Accompanying MemoryCognitive dysfunction in neuropsychiatric disorders: Selected serotonin receptor subtypes as therapeutic targets
2008, Behavioural Brain ResearchSerotonin/dopamine interaction in learning
2008, Progress in Brain ResearchCitation Excerpt :However, an effect of these receptors on learning and memory has been reported. Post-training intraperitoneal administration of the agonist mCPBG impaired retention in autoshaping tests, whereas the antagonists tropisetron and ondansetron improved retention (Hong and Meneses, 1996; Meneses, 2007). Granisetron, another 5-HT3 receptor antagonist, induced deficiencies in spatial learning in a Morris water maze when it was infused intra-hippocampally 20 min before daily training without having any effect on visual discrimination (Naghdi and Harooni, 2005).
The effect of Ondansetron on memory in schizophrenic patients
2005, Brain Research Bulletin
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The receptor nomenclature used in this report is recommended by the Serotonin Club Nomenclature Committee (10). The research was supported by CONACYT Grant 4367-M9406.