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Evaluation of the therapeutic potential of cerebrolysin and/or lithium in the male Wistar rat model of Parkinson’s disease induced by reserpine

Parkinson’s disease (PD) is the second most prevalent neurodegenerative disease worldwide and represents a challenge for clinicians. The present study aims to investigate the effects of cerebrolysin and/or lithium on the behavioral, neurochemical and histopathological alterations induced by reserpin...

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Autores principales: Tharwat, Engy K., Abdelaty, Ahmed O., Abdelrahman, Alaa I., Elsaeed, Hebatallah, Elgohary, Ayatallah, El-Feky, Amena S., Ebrahim, Yasmina M., Sakraan, Alaa, Ismail, Hossam A., Khadrawy, Yasser A., Aboul Ezz, Heba S., Noor, Neveen A., Fahmy, Heba M., Mohammed, Haitham S., Mohammed, Faten F., Radwan, Nasr M., Ahmed, Nawal A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10185619/
https://www.ncbi.nlm.nih.gov/pubmed/36847968
http://dx.doi.org/10.1007/s11011-023-01189-4
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author Tharwat, Engy K.
Abdelaty, Ahmed O.
Abdelrahman, Alaa I.
Elsaeed, Hebatallah
Elgohary, Ayatallah
El-Feky, Amena S.
Ebrahim, Yasmina M.
Sakraan, Alaa
Ismail, Hossam A.
Khadrawy, Yasser A.
Aboul Ezz, Heba S.
Noor, Neveen A.
Fahmy, Heba M.
Mohammed, Haitham S.
Mohammed, Faten F.
Radwan, Nasr M.
Ahmed, Nawal A.
author_facet Tharwat, Engy K.
Abdelaty, Ahmed O.
Abdelrahman, Alaa I.
Elsaeed, Hebatallah
Elgohary, Ayatallah
El-Feky, Amena S.
Ebrahim, Yasmina M.
Sakraan, Alaa
Ismail, Hossam A.
Khadrawy, Yasser A.
Aboul Ezz, Heba S.
Noor, Neveen A.
Fahmy, Heba M.
Mohammed, Haitham S.
Mohammed, Faten F.
Radwan, Nasr M.
Ahmed, Nawal A.
author_sort Tharwat, Engy K.
collection PubMed
description Parkinson’s disease (PD) is the second most prevalent neurodegenerative disease worldwide and represents a challenge for clinicians. The present study aims to investigate the effects of cerebrolysin and/or lithium on the behavioral, neurochemical and histopathological alterations induced by reserpine as a model of PD. The rats were divided into control and reserpine-induced PD model groups. The model animals were further divided into four subgroups: rat PD model, rat PD model treated with cerebrolysin, rat PD model treated with lithium and rat PD model treated with a combination of cerebrolysin and lithium. Treatment with cerebrolysin and/or lithium ameliorated most of the alterations in oxidative stress parameters, acetylcholinesterase and monoamines in the striatum and midbrain of reserpine-induced PD model. It also ameliorated the changes in nuclear factor-kappa and improved the histopathological picture induced by reserpine. It could be suggested that cerebrolysin and/or lithium showed promising therapeutic potential against the variations induced in the reserpine model of PD. However, the ameliorating effects of lithium on the neurochemical, histopathological and behavioral alterations induced by reserpine were more prominent than those of cerebrolysin alone or combined with lithium. It can be concluded that the antioxidant and anti-inflammatory effects of both drugs played a significant role in their therapeutic potency.
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spelling pubmed-101856192023-05-17 Evaluation of the therapeutic potential of cerebrolysin and/or lithium in the male Wistar rat model of Parkinson’s disease induced by reserpine Tharwat, Engy K. Abdelaty, Ahmed O. Abdelrahman, Alaa I. Elsaeed, Hebatallah Elgohary, Ayatallah El-Feky, Amena S. Ebrahim, Yasmina M. Sakraan, Alaa Ismail, Hossam A. Khadrawy, Yasser A. Aboul Ezz, Heba S. Noor, Neveen A. Fahmy, Heba M. Mohammed, Haitham S. Mohammed, Faten F. Radwan, Nasr M. Ahmed, Nawal A. Metab Brain Dis Original Article Parkinson’s disease (PD) is the second most prevalent neurodegenerative disease worldwide and represents a challenge for clinicians. The present study aims to investigate the effects of cerebrolysin and/or lithium on the behavioral, neurochemical and histopathological alterations induced by reserpine as a model of PD. The rats were divided into control and reserpine-induced PD model groups. The model animals were further divided into four subgroups: rat PD model, rat PD model treated with cerebrolysin, rat PD model treated with lithium and rat PD model treated with a combination of cerebrolysin and lithium. Treatment with cerebrolysin and/or lithium ameliorated most of the alterations in oxidative stress parameters, acetylcholinesterase and monoamines in the striatum and midbrain of reserpine-induced PD model. It also ameliorated the changes in nuclear factor-kappa and improved the histopathological picture induced by reserpine. It could be suggested that cerebrolysin and/or lithium showed promising therapeutic potential against the variations induced in the reserpine model of PD. However, the ameliorating effects of lithium on the neurochemical, histopathological and behavioral alterations induced by reserpine were more prominent than those of cerebrolysin alone or combined with lithium. It can be concluded that the antioxidant and anti-inflammatory effects of both drugs played a significant role in their therapeutic potency. Springer US 2023-02-27 2023 /pmc/articles/PMC10185619/ /pubmed/36847968 http://dx.doi.org/10.1007/s11011-023-01189-4 Text en © The Author(s) 2023, Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 Original Article
Tharwat, Engy K.
Abdelaty, Ahmed O.
Abdelrahman, Alaa I.
Elsaeed, Hebatallah
Elgohary, Ayatallah
El-Feky, Amena S.
Ebrahim, Yasmina M.
Sakraan, Alaa
Ismail, Hossam A.
Khadrawy, Yasser A.
Aboul Ezz, Heba S.
Noor, Neveen A.
Fahmy, Heba M.
Mohammed, Haitham S.
Mohammed, Faten F.
Radwan, Nasr M.
Ahmed, Nawal A.
Evaluation of the therapeutic potential of cerebrolysin and/or lithium in the male Wistar rat model of Parkinson’s disease induced by reserpine
title Evaluation of the therapeutic potential of cerebrolysin and/or lithium in the male Wistar rat model of Parkinson’s disease induced by reserpine
title_full Evaluation of the therapeutic potential of cerebrolysin and/or lithium in the male Wistar rat model of Parkinson’s disease induced by reserpine
title_fullStr Evaluation of the therapeutic potential of cerebrolysin and/or lithium in the male Wistar rat model of Parkinson’s disease induced by reserpine
title_full_unstemmed Evaluation of the therapeutic potential of cerebrolysin and/or lithium in the male Wistar rat model of Parkinson’s disease induced by reserpine
title_short Evaluation of the therapeutic potential of cerebrolysin and/or lithium in the male Wistar rat model of Parkinson’s disease induced by reserpine
title_sort evaluation of the therapeutic potential of cerebrolysin and/or lithium in the male wistar rat model of parkinson’s disease induced by reserpine
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10185619/
https://www.ncbi.nlm.nih.gov/pubmed/36847968
http://dx.doi.org/10.1007/s11011-023-01189-4
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