Curcumin protects purkinje neurons, ameliorates motor function and reduces cerebellar atrophy in rat model of cerebellar ataxia induced by 3-AP.


Journal

Journal of chemical neuroanatomy
ISSN: 1873-6300
Titre abrégé: J Chem Neuroanat
Pays: Netherlands
ID NLM: 8902615

Informations de publication

Date de publication:
12 2019
Historique:
received: 13 07 2019
revised: 22 10 2019
accepted: 22 10 2019
pubmed: 2 11 2019
medline: 15 9 2020
entrez: 1 11 2019
Statut: ppublish

Résumé

Cerebellar ataxias comprise a group of terminal illnesses with ataxia as the main symptom. Curcumin as a yellow polyphenol was extracted from the rhizome ofCurcuma longa. Owing to its antioxidant, anti-inflammatory, anti-fibrotic and anti-tumor features, curcumin is considered as a potential therapeutic agent. In this study, we aim to investigate the neuroprotective effects of oral administration of curcumin on a rat model of cerebellar ataxia induced by neurotoxin 3-acetylpyridine. The animals were randomly separated into three groups (control, 3-acetylpyridine, and curcumin + 3-acetylpyridine). Next, motor performance and muscle electromyography activity were assessed. Then, in the molecular part of the study, the anti-apoptotic role of curcumin in cerebellar ataxia and its relationship to protection of Purkinje cells were investigated. Curcumin treatment improved motor coordination and muscular activity, reduced cleaved caspase-3, and increased glutathione level in 3-AP-lesioned rats as well as total volumes of cerebellar granular and molecular layers. the present study implies that curcumin might have neuroprotective effects to counteract neurotoxicity of 3-AP-induced ataxia.

Sections du résumé

BACKGROUND
Cerebellar ataxias comprise a group of terminal illnesses with ataxia as the main symptom. Curcumin as a yellow polyphenol was extracted from the rhizome ofCurcuma longa. Owing to its antioxidant, anti-inflammatory, anti-fibrotic and anti-tumor features, curcumin is considered as a potential therapeutic agent.
AIM
In this study, we aim to investigate the neuroprotective effects of oral administration of curcumin on a rat model of cerebellar ataxia induced by neurotoxin 3-acetylpyridine.
METHODS
The animals were randomly separated into three groups (control, 3-acetylpyridine, and curcumin + 3-acetylpyridine). Next, motor performance and muscle electromyography activity were assessed. Then, in the molecular part of the study, the anti-apoptotic role of curcumin in cerebellar ataxia and its relationship to protection of Purkinje cells were investigated.
RESULTS
Curcumin treatment improved motor coordination and muscular activity, reduced cleaved caspase-3, and increased glutathione level in 3-AP-lesioned rats as well as total volumes of cerebellar granular and molecular layers.
CONCLUSION
the present study implies that curcumin might have neuroprotective effects to counteract neurotoxicity of 3-AP-induced ataxia.

Identifiants

pubmed: 31669431
pii: S0891-0618(19)30128-0
doi: 10.1016/j.jchemneu.2019.101706
pii:
doi:

Substances chimiques

Neuroprotective Agents 0
Pyridines 0
3-acetylpyridine 00QT8FX306
Curcumin IT942ZTH98

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

101706

Informations de copyright

Copyright © 2019 Elsevier B.V. All rights reserved.

Auteurs

Maedeh Mahmoudi (M)

Biology and Anatomical Sciences Department, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran. Electronic address: maede.mahmoudi@yahoo.com.

Amir-Hossein Bayat (AH)

Department of Neuroscience and Psychology, Saveh University of Medical Sciences, Saveh, Iran. Electronic address: a.bayat@yahoo.com.

Mahdi Eskandarian Boroujeni (ME)

Department of Stem Cells and Regenerative Medicine, Faculty of Medical Biotechnology, National Institute of Genetic Engineering and Biotechnology, Tehran, Iran; Department of Human Molecular Genetics, Institute of Molecular Biology and Biotechnology, Faculty of Biology, Adam Mickiewicz University, Poznan, Poland. Electronic address: esmahdee@gmail.com.

Mohammad Amin Abdollahifar (MA)

Biology and Anatomical Sciences Department, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran. Electronic address: m_amin58@yahoo.com.

Vahid Ebrahimi (V)

Department of Anatomy, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran. Electronic address: ebrahimi.v67@gmail.com.

Samira Danyali (S)

Department of Physiology and Neuroscience Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran. Electronic address: samira.danyali@gmail.com.

Mohammad Hassan Heidari (MH)

Biology and Anatomical Sciences Department, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran. Electronic address: heidari34@gmail.com.

Abbas Aliaghaei (A)

Biology and Anatomical Sciences Department, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran. Electronic address: aghaei60@gmail.com.

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Classifications MeSH