The olfactory bulbectomized rat model is not an appropriate model for studying depression based on morphological/stereological studies of the hippocampus
Autor: | Harry W.M. Steinbusch, Tatyana Strekalova, Canan Yurttaş, Christoph Schmitz, Mehmet Turgut |
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Přispěvatelé: | Psychiatrie & Neuropsychologie, RS: MHeNs - R3 - Neuroscience, Faculteit FHML Centraal |
Rok vydání: | 2017 |
Předmět: |
Male
0301 basic medicine medicine.medical_specialty REVERSAL Hippocampal formation Hippocampus Rats Sprague-Dawley NEUROGENESIS 03 medical and health sciences ANTIDEPRESSANT TREATMENT 0302 clinical medicine Neurochemical Fluoxetine ANIMAL-MODEL Internal medicine medicine Animals Major depression Hippocampus (mythology) NEURONS Depressive Disorder General Neuroscience Dentate gyrus Neurogenesis Neurodegeneration NEURODEGENERATION Organ Size medicine.disease Immunohistochemistry Olfactory Bulb Olfactory bulbectomy ALZHEIMERS-DISEASE Disease Models Animal MICE 030104 developmental biology Endocrinology COGNITIVE DEFICITS Astrocytes Antidepressive Agents Second-Generation Antidepressant Psychology Neuroscience BEHAVIOR 030217 neurology & neurosurgery medicine.drug |
Zdroj: | Brain Research Bulletin, 134, 128-135. Elsevier Science |
ISSN: | 0361-9230 |
DOI: | 10.1016/j.brainresbull.2017.07.010 |
Popis: | Bilateral olfactory bulbectomy (OBX) has been used as an animal model for major depression that results in behavioral, neurochemical, and neuroendocrinological changes were reversed by chronic treatment with antidepressants, including fluoxetine. However, both etiological and construct validities are lacking in OBX for rats. In the present study, we investigated the morphological changes in the hippocampi of rats undergoing OBX that were treated with fluoxetine (10 mg/kg, p.o. once daily for 4 and 12 weeks) using stereological techniques. Our results revealed that OBX caused a reduction in the volumes of the CA1/2, CA3, and dentate gyros regions 4 weeks after OBX without fluoxetine treatment. With fluoxetine treatment, these reductions were achieved 12 weeks after OBX and the volumes were comparable to normal control rats. Nevertheless, fluoxetine treatment did not reverse neuron loss in all hippocampal regions 12 weeks after OBX. Therefore, we suggest that the OBX rat model should not be used to detect the antidepressant activity of various pharmacological agents such as fluoxetine. |
Databáze: | OpenAIRE |
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