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Effects of bee venom and dopamine-loaded nanoparticles on reserpine-induced Parkinson’s disease rat model

Parkinson’s disease (PD) is a progressive chronic neurodegenerative condition characterized by the loss of dopaminergic neurons within the substantia nigra. Current PD therapeutic strategies are mainly symptomatic and can lead to motor complications overtime. As a result, alternative medicine may pr...

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Autores principales: Ahmed-Farid, Omar A., Taha, Mohamed, Bakeer, Rofanda M., Radwan, Omyma K., Hendawy, Hassan A. M., Soliman, Ayman S., Yousef, Einas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8551202/
https://www.ncbi.nlm.nih.gov/pubmed/34707203
http://dx.doi.org/10.1038/s41598-021-00764-y
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author Ahmed-Farid, Omar A.
Taha, Mohamed
Bakeer, Rofanda M.
Radwan, Omyma K.
Hendawy, Hassan A. M.
Soliman, Ayman S.
Yousef, Einas
author_facet Ahmed-Farid, Omar A.
Taha, Mohamed
Bakeer, Rofanda M.
Radwan, Omyma K.
Hendawy, Hassan A. M.
Soliman, Ayman S.
Yousef, Einas
author_sort Ahmed-Farid, Omar A.
collection PubMed
description Parkinson’s disease (PD) is a progressive chronic neurodegenerative condition characterized by the loss of dopaminergic neurons within the substantia nigra. Current PD therapeutic strategies are mainly symptomatic and can lead to motor complications overtime. As a result, alternative medicine may provide an effective adjuvant treatment for PD as an addition to or as a replacement of the conventional therapies. The aim of this work was to evaluate the effects of Bee Venom (BV) and dopamine (DA)-loaded nanoparticles in a reserpine-induced animal model of PD. After inducing PD with reserpine injection, different groups of male rats were treated with L-Dopa, BV, DA-nanoparticles. Our findings showed that BV and DA-nanoparticles administration restored monoamines, balanced glutamate/GABA levels, halted DNA fragmentation, decreased pro-inflammatory mediators (IL-1β and TNF-α), and elevated anti-inflammatory mediators (PON1) and neurotropic factor (BDNF) levels in comparison with conventional therapy of PD. Furthermore, in a reserpine-induced PD rat model, the ameliorative effects of BV were significantly superior to that of DA-nanoparticles. These findings imply that BV and DA-nanoparticles could be useful as adjuvant treatments for PD.
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spelling pubmed-85512022021-10-28 Effects of bee venom and dopamine-loaded nanoparticles on reserpine-induced Parkinson’s disease rat model Ahmed-Farid, Omar A. Taha, Mohamed Bakeer, Rofanda M. Radwan, Omyma K. Hendawy, Hassan A. M. Soliman, Ayman S. Yousef, Einas Sci Rep Article Parkinson’s disease (PD) is a progressive chronic neurodegenerative condition characterized by the loss of dopaminergic neurons within the substantia nigra. Current PD therapeutic strategies are mainly symptomatic and can lead to motor complications overtime. As a result, alternative medicine may provide an effective adjuvant treatment for PD as an addition to or as a replacement of the conventional therapies. The aim of this work was to evaluate the effects of Bee Venom (BV) and dopamine (DA)-loaded nanoparticles in a reserpine-induced animal model of PD. After inducing PD with reserpine injection, different groups of male rats were treated with L-Dopa, BV, DA-nanoparticles. Our findings showed that BV and DA-nanoparticles administration restored monoamines, balanced glutamate/GABA levels, halted DNA fragmentation, decreased pro-inflammatory mediators (IL-1β and TNF-α), and elevated anti-inflammatory mediators (PON1) and neurotropic factor (BDNF) levels in comparison with conventional therapy of PD. Furthermore, in a reserpine-induced PD rat model, the ameliorative effects of BV were significantly superior to that of DA-nanoparticles. These findings imply that BV and DA-nanoparticles could be useful as adjuvant treatments for PD. Nature Publishing Group UK 2021-10-27 /pmc/articles/PMC8551202/ /pubmed/34707203 http://dx.doi.org/10.1038/s41598-021-00764-y Text en © The Author(s) 2021, corrected publication 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Ahmed-Farid, Omar A.
Taha, Mohamed
Bakeer, Rofanda M.
Radwan, Omyma K.
Hendawy, Hassan A. M.
Soliman, Ayman S.
Yousef, Einas
Effects of bee venom and dopamine-loaded nanoparticles on reserpine-induced Parkinson’s disease rat model
title Effects of bee venom and dopamine-loaded nanoparticles on reserpine-induced Parkinson’s disease rat model
title_full Effects of bee venom and dopamine-loaded nanoparticles on reserpine-induced Parkinson’s disease rat model
title_fullStr Effects of bee venom and dopamine-loaded nanoparticles on reserpine-induced Parkinson’s disease rat model
title_full_unstemmed Effects of bee venom and dopamine-loaded nanoparticles on reserpine-induced Parkinson’s disease rat model
title_short Effects of bee venom and dopamine-loaded nanoparticles on reserpine-induced Parkinson’s disease rat model
title_sort effects of bee venom and dopamine-loaded nanoparticles on reserpine-induced parkinson’s disease rat model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8551202/
https://www.ncbi.nlm.nih.gov/pubmed/34707203
http://dx.doi.org/10.1038/s41598-021-00764-y
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