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Título: | Modulation of serotonergic function in rat brain by VN2222, a 5-HT reuptake inhibitor with 5-HT1A receptor agonist |
Autor: | Romero, Luz; Celada, Pau CSIC ORCID; Martín-Ruiz, Raúl; Díaz-Mataix, Llorenç; Mourelle, Marisabel; Delgadillo, Joaquim; Hervás, Ildefonso; Artigas, Francesc CSIC ORCID | Palabras clave: | 5-HT1A receptors 5-hydroxytryptamine uptake Antidepressant drugs Dorsal raphe Selective serotonin reuptake inhibitors (SSRIs) Frontal cortex |
Fecha de publicación: | mar-2003 | Editor: | Nature Publishing Group | Citación: | Neuropsychopharmacology 28 (3) : 445-56 (2003) | Resumen: | VN2222 (1-(benzo[b]thiophen-3-yl)-3-[4-(2-methoxiphenyl piperazin-1-yl]propan-1-ol) is a potential antidepressant with high affinity for the serotonin transporter and 5-HT1A receptors. Locally applied, VN2222 enhanced the extracellular 5-hydroxytryptamine (5-HT) concentration (5-HText) in rat striatum to 780% of baseline whereas its systemic administration (1–10 mg/kg s.c.) reduced 5-HText. In the presence of citalopram, 8-OH-DPAT or VN2222 applied in medial prefrontal cortex reduced 5-HText. Fluoxetine, VN2222, and 8-OH-DPAT suppressed the firing rate of dorsal raphe 5-HT neurons (ED50: 790, 14.9, and 0.8 g/kg i.v., respectively). These effects were antagonized by WAY 100635. Administration of VN2222 for 2 weeks desensitized 5-HT1A receptors as assessed by microdialysis and single-unit recordings (ED50 values for 8-OH-DPAT were 0.45 and 2.34 g/kg i.v. for controls and rats treated with 6 mg/kg day VN2222). These results show that VN2222 is a mixed 5-HT reuptake inhibitor/5-HT1A agonist that markedly desensitizes 5-HT1A autoreceptors. These properties suggest that it may be a clinically effective dual action antidepressant drug. | Versión del editor: | http://dx.doi.org/10.1038/sj.npp.1300062 | URI: | http://hdl.handle.net/10261/34694 | DOI: | 10.1038/sj.npp.1300062 | ISSN: | 0893-133X | E-ISSN: | 1740-634X |
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