Synergistic effect between prelimbic 5-HT3 and CB1 receptors on memory consolidation deficit in adult male Sprague-Dawley rats: An isobologram analysis
Autor: | Mohammad-Reza Zarrindast, M. Emam Ghoreishi, Mohammad Nasehi, Nargol Ahmadi-Mahmoodabadi |
---|---|
Rok vydání: | 2015 |
Předmět: |
0301 basic medicine
Agonist Male medicine.drug_class medicine.medical_treatment Biguanides Arachidonic Acids Pharmacology Motor Activity Serotonergic Rats Sprague-Dawley 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Receptor Cannabinoid CB1 Oxazines medicine Avoidance Learning Reaction Time Serotonin receptor antagonist Animals Arachidonylcyclopropylamide Serotonin receptor agonist Cannabinoid Receptor Agonists Cerebral Cortex Memory Disorders Dose-Response Relationship Drug Chemistry General Neuroscience Drug Synergism Bridged Bicyclo Compounds Heterocyclic Rats Serotonin Receptor Agonists Disease Models Animal 030104 developmental biology Memory consolidation Serotonin Cannabinoid Serotonin Antagonists Receptors Serotonin 5-HT3 Neuroscience 030217 neurology & neurosurgery medicine.drug |
Zdroj: | Neuroscience. 317 |
ISSN: | 1873-7544 |
Popis: | The serotonergic system has often been defined as a neuromodulator system, and is specifically involved in learning and memory via its various receptors. Serotonin is involved in many of the same processes affected by cannabinoids. The present study investigated the influence of bilateral post-training intra-prelimbic (PL) administrations of serotonergic 5-hydroxytryptamine type-3 (5-HT3) receptor agents on arachidonylcyclopropylamide (ACPA) (cannabinoid CB1 receptor agonist)-induced amnesia, using the step-through inhibitory avoidance (IA) task to assess memory in adult male Sprague-Dawley rats. The results indicated that sole intra-PL microinjection of ACPA (0.1 and 0.5 μg/rat) and 5-HT3 serotonin receptor agonist (m-Chlorophenylbiguanide hydrochloride, m-CPBG; 0.001, 0.01 and 0.1 μg/rat) impaired, whereas Y-25130 (a selective 5-HT3 serotonin receptor antagonist; 0.001 and 0.01 and 0.1 μg/rat) did not alter IA memory consolidation, by itself. Moreover, intra-PL administration of subthreshold dose of m-CPBG (0.0005 μg/rat) potentiated, while Y-25130 (0. 1 μg/rat) restored ACPA-induced memory consolidation deficit. The isobologram analysis showed that there is a synergistic effect between ACPA and m-CPBG on memory consolidation deficit. These findings suggest that 5-HT3 receptor mechanism(s), at least partly, play(s) a role in modulating the effect of ACPA on memory consolidation in the PL area. |
Databáze: | OpenAIRE |
Externí odkaz: |