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Fraternine, a Novel Wasp Peptide, Protects against Motor Impairments in 6-OHDA Model of Parkinsonism

Parkinson’s disease (PD) is a progressive neurodegenerative condition that affects the Central Nervous System (CNS). Insect venoms show high molecular variability and selectivity in the CNS of mammals and present potential for the development of new drugs for the treatment of PD. In this study, we i...

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Autores principales: Biolchi, Andréia Mayer, de Oliveira, Danilo Gustavo Rodrigues, Amaral, Henrique de Oliveira, Campos, Gabriel Avohay Alves, Gonçalves, Jacqueline Coimbra, de Souza, Adolfo Carlos Barros, Lima, Marcos Robalinho, Silva, Luciano Paulino, Mortari, Márcia Renata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7551070/
https://www.ncbi.nlm.nih.gov/pubmed/32867207
http://dx.doi.org/10.3390/toxins12090550
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author Biolchi, Andréia Mayer
de Oliveira, Danilo Gustavo Rodrigues
Amaral, Henrique de Oliveira
Campos, Gabriel Avohay Alves
Gonçalves, Jacqueline Coimbra
de Souza, Adolfo Carlos Barros
Lima, Marcos Robalinho
Silva, Luciano Paulino
Mortari, Márcia Renata
author_facet Biolchi, Andréia Mayer
de Oliveira, Danilo Gustavo Rodrigues
Amaral, Henrique de Oliveira
Campos, Gabriel Avohay Alves
Gonçalves, Jacqueline Coimbra
de Souza, Adolfo Carlos Barros
Lima, Marcos Robalinho
Silva, Luciano Paulino
Mortari, Márcia Renata
author_sort Biolchi, Andréia Mayer
collection PubMed
description Parkinson’s disease (PD) is a progressive neurodegenerative condition that affects the Central Nervous System (CNS). Insect venoms show high molecular variability and selectivity in the CNS of mammals and present potential for the development of new drugs for the treatment of PD. In this study, we isolated and identified a component of the venom of the social wasp Parachartergus fraternus and evaluated its neuroprotective activity in the murine model of PD. For this purpose, the venom was filtered and separated through HPLC; fractions were analyzed through mass spectrometry and the active fraction was identified as a novel peptide, called Fraternine. We performed two behavioral tests to evaluate motor discoordination, as well as an apomorphine-induced rotation test. We also conducted an immunohistochemical assay to assess protection in TH+ neurons in the Substantia Nigra (SN) region. Group treated with 10 μg/animal of Fraternine remained longer in the rotarod compared to the lesioned group. In the apomorphine test, Fraternine decreased the number of rotations between treatments. This dose also inhibited dopaminergic neuronal loss, as indicated by immunohistochemical analysis. This study identified a novel peptide able to prevent the death of dopaminergic neurons of the SN and recover motor deficit in a 6-OHDA-induced murine model of PD.
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spelling pubmed-75510702020-10-16 Fraternine, a Novel Wasp Peptide, Protects against Motor Impairments in 6-OHDA Model of Parkinsonism Biolchi, Andréia Mayer de Oliveira, Danilo Gustavo Rodrigues Amaral, Henrique de Oliveira Campos, Gabriel Avohay Alves Gonçalves, Jacqueline Coimbra de Souza, Adolfo Carlos Barros Lima, Marcos Robalinho Silva, Luciano Paulino Mortari, Márcia Renata Toxins (Basel) Article Parkinson’s disease (PD) is a progressive neurodegenerative condition that affects the Central Nervous System (CNS). Insect venoms show high molecular variability and selectivity in the CNS of mammals and present potential for the development of new drugs for the treatment of PD. In this study, we isolated and identified a component of the venom of the social wasp Parachartergus fraternus and evaluated its neuroprotective activity in the murine model of PD. For this purpose, the venom was filtered and separated through HPLC; fractions were analyzed through mass spectrometry and the active fraction was identified as a novel peptide, called Fraternine. We performed two behavioral tests to evaluate motor discoordination, as well as an apomorphine-induced rotation test. We also conducted an immunohistochemical assay to assess protection in TH+ neurons in the Substantia Nigra (SN) region. Group treated with 10 μg/animal of Fraternine remained longer in the rotarod compared to the lesioned group. In the apomorphine test, Fraternine decreased the number of rotations between treatments. This dose also inhibited dopaminergic neuronal loss, as indicated by immunohistochemical analysis. This study identified a novel peptide able to prevent the death of dopaminergic neurons of the SN and recover motor deficit in a 6-OHDA-induced murine model of PD. MDPI 2020-08-27 /pmc/articles/PMC7551070/ /pubmed/32867207 http://dx.doi.org/10.3390/toxins12090550 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Biolchi, Andréia Mayer
de Oliveira, Danilo Gustavo Rodrigues
Amaral, Henrique de Oliveira
Campos, Gabriel Avohay Alves
Gonçalves, Jacqueline Coimbra
de Souza, Adolfo Carlos Barros
Lima, Marcos Robalinho
Silva, Luciano Paulino
Mortari, Márcia Renata
Fraternine, a Novel Wasp Peptide, Protects against Motor Impairments in 6-OHDA Model of Parkinsonism
title Fraternine, a Novel Wasp Peptide, Protects against Motor Impairments in 6-OHDA Model of Parkinsonism
title_full Fraternine, a Novel Wasp Peptide, Protects against Motor Impairments in 6-OHDA Model of Parkinsonism
title_fullStr Fraternine, a Novel Wasp Peptide, Protects against Motor Impairments in 6-OHDA Model of Parkinsonism
title_full_unstemmed Fraternine, a Novel Wasp Peptide, Protects against Motor Impairments in 6-OHDA Model of Parkinsonism
title_short Fraternine, a Novel Wasp Peptide, Protects against Motor Impairments in 6-OHDA Model of Parkinsonism
title_sort fraternine, a novel wasp peptide, protects against motor impairments in 6-ohda model of parkinsonism
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7551070/
https://www.ncbi.nlm.nih.gov/pubmed/32867207
http://dx.doi.org/10.3390/toxins12090550
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