Fluoxetine administration modulates the cytoskeletal microtubular system in the rat hippocampus
Version of Record online: 12 JAN 2009
Copyright © 2009 Wiley-Liss, Inc.
Volume 63, Issue 4, pages 359–364, April 2009
How to Cite
Bianchi, M., Shah, A. J., Fone, K. C.F., Atkins, A. R., Dawson, L. A., Heidbreder, C. A., Hows, M. E., Hagan, J. J. and Marsden, C. A. (2009), Fluoxetine administration modulates the cytoskeletal microtubular system in the rat hippocampus. Synapse, 63: 359–364. doi: 10.1002/syn.20614
- Issue online: 12 JAN 2009
- Version of Record online: 12 JAN 2009
- Manuscript Accepted: 2 SEP 2008
- Manuscript Received: 6 MAY 2008
- University of Nottingham and GlaxoSmithKline plc (MB)
- neuronal plasticity;
A number of studies suggest that stressful conditions can induce structural alterations in the hippocampus and that antidepressant drugs may prevent such deficits. In particular, the selective serotonin reuptake inhibitor (SSRI) fluoxetine was more effective in modulating different neuronal plasticity phenomena and related molecules in rat hippocampus. Cytoskeletal microtubule dynamics are fundamental to dendrites and axons remodeling, leading to the hypothesis that fluoxetine may affect the microtubular system. However, despite reports of stress-induced alterations in microtubule dynamics by different stressors, only few studies investigated the in vivo effects of antidepressants on microtubules in specific rat brain regions. The present study investigated the dose-related (1, 5, or 10 mg/kg i.p.) effects of acute and chronic (21 days) treatments with fluoxetine on the ratio of hippocampal α-tubulin isoforms which is thought to reflect microtubule dynamics. Western Blot analysis was used to quantify α-tubulin isoforms, high-performance liquid chromatography and fluorescence detection was used to measure ex vivo monoamine metabolism. The results showed that acute fluoxetine increased the stable forms acetylated and detyrosinated α-tubulin. Conversely, chronic fluoxetine decreased acetylated α-tubulin, indicative of increased microtubule dynamics. The neuron-specific Δ2-Tubulin was increased by chronic fluoxetine indicating neuronal involvement in the observed cytoskeletal changes. Although acute and chronic fluoxetine similarly altered serotonin metabolism by inhibition of serotonin reuptake, this showed no apparent correlation to the cytoskeletal perturbations. Our findings demonstrate that fluoxetine administration modulates microtubule dynamics in rat hippocampus. The cytoskeletal effect exerted by fluoxetine may eventually culminate in promoting events of structural neuronal remodeling. Synapse 63:359–364, 2009. © 2009 Wiley-Liss, Inc.