Effects of the association of physical stress and chronic use of fluoxetine hydrochloride on the cerebral cortex
DOI:
https://doi.org/10.33448/rsd-v10i11.19509Keywords:
Cerebral cortex; Physical stress; Fluoxetine hydrochloride.Abstract
Exposure to stressful factors plays an important role in development of depressive disorders. The deleterious effects of stress on neuroplasticity and apoptosis can be accentuated by chronic use of antidepressants. Thus, this study aims to evaluate and correlate the effects and consequences of physical stress (PS), associated with the treatment of fluoxetine hydrochloride (FC), on brain volume and cortical thickness of three brain areas. Brains of 25 male Wistar rats (Rattus norvegicus) were used. These animals were divided into 5 groups: G1 – control group; G2 – FC and without PS; G3 – PS but without FC; G4 –FC until the day before surgical procedure (PS); and G5 – Animals treated with FC until 30 days after surgical procedure (PS). The results show that groups G3, G4 and G5 had a significant reduction in brain volume. Regarding cortical thickness in limbic area, the data show that groups G4 and G5 had a significant reduction compared to G1, as well as groups G3, G4 and G5 showed a significant difference compared to G2. In the sensitive area, groups G3, G4 and G5 had a significant reduction when compared to G1; the same was observed for G4 and G5 in relation to groups G2 and G3. In the motor area, a similar result was observed in groups G3 and G4 in relation to G1. The data allow to conclude that physical stress, associated or not with chronic use of fluoxetine hydrochloride, decreases the cortical volume of male rats brain and, as a consequence of reduction, there is a significant loss of cortical density in limbic, sensory and motor areas.
References
Ackerley, R., Aimonetti, J. M., & Ribot-Ciscar, E. (2017). Emotions alter muscle proprioceptive coding of movements in humans. Scientific Reports, 7(1), 1–9. https://doi.org/10.1038/s41598-017-08721-4
Aoki, S., Smith, J. B., Li, H., Yan, X., Igarashi, M., Coulon, P., Wickens, J. R., Ruigrok, T. J., & Jin, X. (2019). An open cortico-basal ganglia loop allows limbic control over motor output via the nigrothalamic pathway. ELife, 8. https://doi.org/10.7554/eLife.49995
Benfield, P., Heel, R. C., & Lewis, S. P. (1986). Fluoxetine. Drugs, 32(6), 481–508. https://doi.org/10.2165/00003495-198632060-00002
Bloss, E. B., Janssen, W. G., McEwen, B. S., & Morrison, J. H. (2010). Interactive effects of stress and aging on structural plasticity in the prefrontal cortex. Journal of Neuroscience, 30(19), 6726–6731. https://doi.org/10.1523/JNEUROSCI.0759-10.2010
Bosman, R. C., Waumans, R. C., Jacobs, G. E., Oude Voshaar, R. C., Muntingh, A. D. T., Batelaan, N. M., & van Balkom, A. J. L. M. (2018). Failure to Respond after Reinstatement of Antidepressant Medication: A Systematic Review. Psychotherapy and Psychosomatics, 87(5), 268–275. https://doi.org/10.1159/000491550
Bremner, J. D. (2006). Stress and brain atrophy. CNS & Neurological Disorders Drug Targets, 5(5), 503–512. http://www.ncbi.nlm.nih.gov/pubmed/17073653%5Cnhttp://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=PMC3269810
Chrousos, G. P., & Gold, P. W. (1992). The Concepts of Stress and Stress System Disorders: Overview of Physical and Behavioral Homeostasis. JAMA, 267(9), 1244–1252. https://doi.org/10.1001/jama.1992.03480090092034
Czéh, B., Müller-Keuker, J. I. H., Rygula, R., Abumaria, N., Hiemke, C., Domenici, E., & Fuchs, E. (2007). Chronic social stress inhibits cell proliferation in the adult medial prefrontal cortex: Hemispheric asymmetry and reversal by fluoxetine treatment. Neuropsychopharmacology, 32(7), 1490–1503. https://doi.org/10.1038/sj.npp.1301275
Djordjevic, A., Djordjevic, J., Elaković, I., Adzic, M., Matić, G., & Radojcic, M. B. (2012). Effects of fluoxetine on plasticity and apoptosis evoked by chronic stress in rat prefrontal cortex. European Journal of Pharmacology, 693(1–3), 37–44. https://doi.org/10.1016/j.ejphar.2012.07.042
Feighner, J. P. (1999). Mechanism of action of antidepressant medications. The Journal of Clinical Psychiatry, 60 Suppl 4, 3–4.
Firk, C., & Markus, C. R. (2006). Review: Serotonin by stress interaction: a susceptibility factor for the development of depression? Journal of Psychopharmacology, 21(5), 538–544. https://doi.org/10.1177/0269881106075588
Fleck, M. P., Berlim, M. T., Lafer, B., Sougey, E. B., Del Porto, J. A., Brasil, M. A., Juruena, M. F., & Hetem, L. A. (2009). [Review of the guidelines of the Brazilian Medical Association for the treatment of depression (Complete version)]. Revista Brasileira de Psiquiatria (Sao Paulo, Brazil : 1999), 31 Suppl 1, S7-17. https://doi.org/10.1590/S1516-44462009000500003
Gárate, I., Garcia-Bueno, B., Madrigal, J. L. M., Caso, J. R., Alou, L., Gomez-Lus, M. L., Micó, J. A., & Leza, J. C. (2013). Stress-induced neuroinflammation: Role of the toll-like receptor-4 pathway. Biological Psychiatry, 73(1), 32–43. https://doi.org/10.1016/j.biopsych.2012.07.005
Gingrich, J. A., & Hen, R. (2001). Dissecting the role of the serotonin system in neuropsychiatric disorders using knockout mice. Psychopharmacology, 155(1), 1–10. https://doi.org/10.1007/s002130000573
Hwang, S., & Kim, J.-K. (2020). Fluoxetine Induces Apoptotic and Oxidative Neuronal Death Associated with The Influx of Copper Ions in Cultured Neuronal Cells. Chonnam Medical Journal, 56(1), 20. https://doi.org/10.4068/cmj.2020.56.1.20
McAllister, B. B., Spanswick, S. C., Patel, P. P., Barneto, A. A., & Dyck, R. H. (2015). The effects of chronic fluoxetine treatment following injury of medial frontal cortex in mice. Behavioural Brain Research, 290, 102–116. https://doi.org/10.1016/j.bbr.2015.04.049
Oquendo, M. A., Echavarria, G., Galfalvy, H. C., Grunebaum, M. F., Burke, A., Barrera, A., Cooper, T. B., Malone, K. M., & Mann, J. J. (2003). Lower cortisol levels in depressed patients with comorbid post-traumatic stress disorder. Neuropsychopharmacology, 28(3), 591–598. https://doi.org/10.1038/sj.npp.1300050
Santarelli, L., Saxe, M., Gross, C., Surget, A., Battaglia, F., Dulawa, S., Weisstaub, N., Lee, J., Duman, R., Arancio, O., Belzung, C., & Hen, R. (2003). Requirement of hippocampal neurogenesis for the behavioral effects of antidepressants. Science (New York, N.Y.), 301(5634), 805–809. https://doi.org/10.1126/science.1083328
Silva, D. K., & De, F. M. (2008). Pharmacogenetics of selective serotonine reuptake inhibitors: A review [Portuguese] Farmacogenetica de inibidores seletivos de recaptacao de serotonina: Uma revisao. Revista de Psiquiatria Do Rio Grande Do Sul, 30(1 SUPPL.).
Sousa, N., Lukoyanov, N. V, Madeira, M. D., Almeida, O. F., & Paula-Barbosa, M. M. (2000). Reorganization of the morphology of hippocampal neurites and synapses after stress-induced damage correlates with behavioral improvement. Neuroscience, 97(2), 253–266. https://doi.org/10.1016/s0306-4522(00)00050-6
Veena, J., Rao, B. S. S., & Srikumar, B. N. (2011). Regulation of adult neurogenesis in the hippocampus by stress, acetylcholine and dopamine. Journal of Natural Science, Biology, and Medicine, 2(1), 26–37. https://doi.org/10.4103/0976-9668.82312
White, K. J., Walline, C. C., & Barker, E. L. (2005). Serotonin transporters: implications for antidepressant drug development. The AAPS Journal, 7(2), E421-33. https://doi.org/10.1208/aapsj070242
Wulf, G., & Lewthwaite, R. (2016). Optimizing performance through intrinsic motivation and attention for learning: The OPTIMAL theory of motor learning. Psychonomic Bulletin and Review, 23(5), 1382–1414. https://doi.org/10.3758/s13423-015-0999-9
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