Effect of 5-HT6 Receptor Ligands Combined with Haloperidol or Risperidone on Antidepressant-/Anxiolytic-Like Behavior and BDNF Regulation in Hippocampus and Prefrontal Cortex of Rats
Anna Wesołowska,1 Joanna Rychtyk,1 Joanna Gdula-Argasińska,2 Katarzyna Górecka,1 Natalia Wilczyńska-Zawal,1 Magdalena Jastrzębska-Więsek,1 Anna Partyka1 1Department of Clinical Pharmacy, Faculty of Pharmacy, Jagiellonian University Medical College...
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| Formato: | article |
| Lenguaje: | EN |
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Dove Medical Press
2021
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| Acceso en línea: | https://doaj.org/article/0698d54e34d4401ab7e961b71676cadf |
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| Sumario: | Anna Wesołowska,1 Joanna Rychtyk,1 Joanna Gdula-Argasińska,2 Katarzyna Górecka,1 Natalia Wilczyńska-Zawal,1 Magdalena Jastrzębska-Więsek,1 Anna Partyka1 1Department of Clinical Pharmacy, Faculty of Pharmacy, Jagiellonian University Medical College, Kraków, Poland; 2Department of Radioligands, Faculty of Pharmacy, Jagiellonian University Medical College, Kraków, PolandCorrespondence: Anna PartykaDepartment of Clinical Pharmacy, Faculty of Pharmacy, Jagiellonian University Medical College, Medyczna 9 Street, Kraków, 30-688, PolandTel/Fax +48 126 205 654Email annairena.partyka@uj.edu.plBackground: The presence of depressive and anxiety symptoms in patients with schizophrenia may have an important impact on treatment and compliance. Hence, interventions addressing such comorbidity in schizophrenia should be explored. One target may be a serotonergic 5-HT6 receptor (5-HT6R) since its ligands displayed antidepressant- and anxiolytic-like activities in preclinical experiments.Methods: Acute and chronic (21 days) administration of haloperidol or risperidone in combination with a selective 5-HT6R agonist (WAY-181187) or antagonist (SB-742457) to rats was performed for detecting antidepressant- and anxiolytic-like behaviors. In addition, the level of brain-derived neurotrophic factor (BDNF) protein and its gene expression in hippocampus and prefrontal cortex were determined.Results: Both single and chronic administration of WAY-181187 with haloperidol produced antidepressant- and anxiolytic-like activities. SB-742457 did not provide full benefits in terms of improvement of haloperidol-induced adverse mood effects. However, the administration of SB-742457 with risperidone triggered its anxiolytic-like activity. Both 5-HT6R ligands evoked no changes in haloperidol-induced effects on BDNF level. WAY-181187 induced repression of the BDNF gene while SB-742457 increased its expression in both structures. 5-HT6R ligands, when combined with risperidone, did not change BDNF protein level and increased gene expression in the hippocampus, while they elevated BDNF level and potentiated gene expression in the prefrontal cortex.Conclusion: The combined administration of WAY-181187 and haloperidol provided the greatest benefits, which were manifested by antidepressant-like effects and suppression of the anxiogenic-like properties. The combined administration of risperidone with both agonist and antagonist resulted only in an anxiolytic-like effect. It seems that the anxiolytic-like effects induced by haloperidol or risperidone with the addition of 5-HT6R ligands are task-specific. The data on BDNF protein and gene expression did not fully correspond with the behavioral outcomes, and thus it appears that other factors/mechanisms are involved in the observed antidepressant- and/or anxiolytic-like effects.Keywords: schizophrenia, haloperidol, risperidone, 5-HT6 receptor ligands, BDNF, rats |
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