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Neuropathology of the Basal Ganglia in SNCA Transgenic Rat Model of Parkinson’s Disease: Involvement of Parvalbuminergic Interneurons and Glial-Derived Neurotropic Factor
Parkinson’s disease (PD) is a neurodegenerative disease characterized by the accumulation of alpha-synuclein, encoded by the SNCA gene. The main neuropathological hallmark of PD is the degeneration of dopaminergic neurons leading to striatal dopamine depletion. Trophic support by a neurotrophin call...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9456397/ https://www.ncbi.nlm.nih.gov/pubmed/36077524 http://dx.doi.org/10.3390/ijms231710126 |
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author | Paldino, Emanuela D’angelo, Vincenza Massaro Cenere, Mariangela Guatteo, Ezia Barattucci, Simone Migliorato, Giorgia Berretta, Nicola Riess, Olaf Sancesario, Giuseppe Mercuri, Nicola Biagio Fusco, Francesca Romana |
author_facet | Paldino, Emanuela D’angelo, Vincenza Massaro Cenere, Mariangela Guatteo, Ezia Barattucci, Simone Migliorato, Giorgia Berretta, Nicola Riess, Olaf Sancesario, Giuseppe Mercuri, Nicola Biagio Fusco, Francesca Romana |
author_sort | Paldino, Emanuela |
collection | PubMed |
description | Parkinson’s disease (PD) is a neurodegenerative disease characterized by the accumulation of alpha-synuclein, encoded by the SNCA gene. The main neuropathological hallmark of PD is the degeneration of dopaminergic neurons leading to striatal dopamine depletion. Trophic support by a neurotrophin called glial-derived neurotrophic factor (GDNF) is also lacking in PD. We performed immunohistochemical studies to investigate neuropathological changes in the basal ganglia of a rat transgenic model of PD overexpressing alfa-synuclein. We observed that neuronal loss also occurs in the dorsolateral part of the striatum in the advanced stages of the disease. Moreover, along with the degeneration of the medium spiny projection neurons, we found a dramatic loss of parvalbumin interneurons. A marked decrease in GDNF, which is produced by parvalbumin interneurons, was observed in the striatum and in the substantia nigra of these animals. This confirmed the involvement of the striatum in the pathophysiology of PD and the importance of GDNF in maintaining the health of the substantia nigra. |
format | Online Article Text |
id | pubmed-9456397 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-94563972022-09-09 Neuropathology of the Basal Ganglia in SNCA Transgenic Rat Model of Parkinson’s Disease: Involvement of Parvalbuminergic Interneurons and Glial-Derived Neurotropic Factor Paldino, Emanuela D’angelo, Vincenza Massaro Cenere, Mariangela Guatteo, Ezia Barattucci, Simone Migliorato, Giorgia Berretta, Nicola Riess, Olaf Sancesario, Giuseppe Mercuri, Nicola Biagio Fusco, Francesca Romana Int J Mol Sci Article Parkinson’s disease (PD) is a neurodegenerative disease characterized by the accumulation of alpha-synuclein, encoded by the SNCA gene. The main neuropathological hallmark of PD is the degeneration of dopaminergic neurons leading to striatal dopamine depletion. Trophic support by a neurotrophin called glial-derived neurotrophic factor (GDNF) is also lacking in PD. We performed immunohistochemical studies to investigate neuropathological changes in the basal ganglia of a rat transgenic model of PD overexpressing alfa-synuclein. We observed that neuronal loss also occurs in the dorsolateral part of the striatum in the advanced stages of the disease. Moreover, along with the degeneration of the medium spiny projection neurons, we found a dramatic loss of parvalbumin interneurons. A marked decrease in GDNF, which is produced by parvalbumin interneurons, was observed in the striatum and in the substantia nigra of these animals. This confirmed the involvement of the striatum in the pathophysiology of PD and the importance of GDNF in maintaining the health of the substantia nigra. MDPI 2022-09-04 /pmc/articles/PMC9456397/ /pubmed/36077524 http://dx.doi.org/10.3390/ijms231710126 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Paldino, Emanuela D’angelo, Vincenza Massaro Cenere, Mariangela Guatteo, Ezia Barattucci, Simone Migliorato, Giorgia Berretta, Nicola Riess, Olaf Sancesario, Giuseppe Mercuri, Nicola Biagio Fusco, Francesca Romana Neuropathology of the Basal Ganglia in SNCA Transgenic Rat Model of Parkinson’s Disease: Involvement of Parvalbuminergic Interneurons and Glial-Derived Neurotropic Factor |
title | Neuropathology of the Basal Ganglia in SNCA Transgenic Rat Model of Parkinson’s Disease: Involvement of Parvalbuminergic Interneurons and Glial-Derived Neurotropic Factor |
title_full | Neuropathology of the Basal Ganglia in SNCA Transgenic Rat Model of Parkinson’s Disease: Involvement of Parvalbuminergic Interneurons and Glial-Derived Neurotropic Factor |
title_fullStr | Neuropathology of the Basal Ganglia in SNCA Transgenic Rat Model of Parkinson’s Disease: Involvement of Parvalbuminergic Interneurons and Glial-Derived Neurotropic Factor |
title_full_unstemmed | Neuropathology of the Basal Ganglia in SNCA Transgenic Rat Model of Parkinson’s Disease: Involvement of Parvalbuminergic Interneurons and Glial-Derived Neurotropic Factor |
title_short | Neuropathology of the Basal Ganglia in SNCA Transgenic Rat Model of Parkinson’s Disease: Involvement of Parvalbuminergic Interneurons and Glial-Derived Neurotropic Factor |
title_sort | neuropathology of the basal ganglia in snca transgenic rat model of parkinson’s disease: involvement of parvalbuminergic interneurons and glial-derived neurotropic factor |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9456397/ https://www.ncbi.nlm.nih.gov/pubmed/36077524 http://dx.doi.org/10.3390/ijms231710126 |
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