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Axon morphology of rapid Golgi-stained pyramidal neurons in the prefrontal cortex in schizophrenia
AIM: To analyze axon morphology on rapid Golgi impregnated pyramidal neurons in the dorsolateral prefrontal cortex in schizophrenia. METHODS: Postmortem brain tissue from five subjects diagnosed with schizophrenia and five control subjects without neuropathological findings was processed with the ra...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Croatian Medical Schools
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7480760/ https://www.ncbi.nlm.nih.gov/pubmed/32881434 http://dx.doi.org/10.3325/cmj.2020.61.354 |
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author | Banovac, Ivan Sedmak, Dora Rojnić Kuzman, Martina Hladnik, Ana Petanjek, Zdravko |
author_facet | Banovac, Ivan Sedmak, Dora Rojnić Kuzman, Martina Hladnik, Ana Petanjek, Zdravko |
author_sort | Banovac, Ivan |
collection | PubMed |
description | AIM: To analyze axon morphology on rapid Golgi impregnated pyramidal neurons in the dorsolateral prefrontal cortex in schizophrenia. METHODS: Postmortem brain tissue from five subjects diagnosed with schizophrenia and five control subjects without neuropathological findings was processed with the rapid Golgi method. Layer III and layer V pyramidal neurons from Brodmann area 9 were chosen in each brain for reconstruction with Neurolucida software. The axons and cell bodies of 136 neurons from subjects with schizophrenia and of 165 neurons from control subjects were traced. The data obtained by quantitative analysis were compared between the schizophrenia and control group with the t test. RESULTS: Axon impregnation length was consistently greater in the schizophrenia group. The axon main trunk length was significantly greater in the schizophrenia than in the control group (93.7 ± 36.6 μm vs 49.8 ± 9.9 μm, P = 0.032). Furthermore, in the schizophrenia group more axons had visibly stained collaterals (14.7% vs 5.5%). CONCLUSION: Axon rapid Golgi impregnation stops at the beginning of the myelin sheath. The increased axonal staining in the schizophrenia group could, therefore, be explained by reduced axon myelination. Such a decrease in axon myelination is in line with both the disconnection hypothesis and the two-hit model of schizophrenia as a neurodevelopmental disease. Our results support that the cortical circuitry disorganization in schizophrenia might be caused by functional alterations of two major classes of principal neurons due to altered oligodendrocyte development. |
format | Online Article Text |
id | pubmed-7480760 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Croatian Medical Schools |
record_format | MEDLINE/PubMed |
spelling | pubmed-74807602020-09-17 Axon morphology of rapid Golgi-stained pyramidal neurons in the prefrontal cortex in schizophrenia Banovac, Ivan Sedmak, Dora Rojnić Kuzman, Martina Hladnik, Ana Petanjek, Zdravko Croat Med J Research Article AIM: To analyze axon morphology on rapid Golgi impregnated pyramidal neurons in the dorsolateral prefrontal cortex in schizophrenia. METHODS: Postmortem brain tissue from five subjects diagnosed with schizophrenia and five control subjects without neuropathological findings was processed with the rapid Golgi method. Layer III and layer V pyramidal neurons from Brodmann area 9 were chosen in each brain for reconstruction with Neurolucida software. The axons and cell bodies of 136 neurons from subjects with schizophrenia and of 165 neurons from control subjects were traced. The data obtained by quantitative analysis were compared between the schizophrenia and control group with the t test. RESULTS: Axon impregnation length was consistently greater in the schizophrenia group. The axon main trunk length was significantly greater in the schizophrenia than in the control group (93.7 ± 36.6 μm vs 49.8 ± 9.9 μm, P = 0.032). Furthermore, in the schizophrenia group more axons had visibly stained collaterals (14.7% vs 5.5%). CONCLUSION: Axon rapid Golgi impregnation stops at the beginning of the myelin sheath. The increased axonal staining in the schizophrenia group could, therefore, be explained by reduced axon myelination. Such a decrease in axon myelination is in line with both the disconnection hypothesis and the two-hit model of schizophrenia as a neurodevelopmental disease. Our results support that the cortical circuitry disorganization in schizophrenia might be caused by functional alterations of two major classes of principal neurons due to altered oligodendrocyte development. Croatian Medical Schools 2020-08 /pmc/articles/PMC7480760/ /pubmed/32881434 http://dx.doi.org/10.3325/cmj.2020.61.354 Text en Copyright © 2020 by the Croatian Medical Journal. All rights reserved. http://creativecommons.org/licenses/by/2.5/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Banovac, Ivan Sedmak, Dora Rojnić Kuzman, Martina Hladnik, Ana Petanjek, Zdravko Axon morphology of rapid Golgi-stained pyramidal neurons in the prefrontal cortex in schizophrenia |
title | Axon morphology of rapid Golgi-stained pyramidal neurons in the prefrontal cortex in schizophrenia |
title_full | Axon morphology of rapid Golgi-stained pyramidal neurons in the prefrontal cortex in schizophrenia |
title_fullStr | Axon morphology of rapid Golgi-stained pyramidal neurons in the prefrontal cortex in schizophrenia |
title_full_unstemmed | Axon morphology of rapid Golgi-stained pyramidal neurons in the prefrontal cortex in schizophrenia |
title_short | Axon morphology of rapid Golgi-stained pyramidal neurons in the prefrontal cortex in schizophrenia |
title_sort | axon morphology of rapid golgi-stained pyramidal neurons in the prefrontal cortex in schizophrenia |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7480760/ https://www.ncbi.nlm.nih.gov/pubmed/32881434 http://dx.doi.org/10.3325/cmj.2020.61.354 |
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