NF-κB Inhibitors Attenuate MCAO Induced Neurodegeneration and Oxidative Stress-A Reprofiling Approach.

MCAO stroke atorvastatin caeffic acid phenethyl ester cephalexin mycophenolate p-NF-κB reprofiling

Journal

Frontiers in molecular neuroscience
ISSN: 1662-5099
Titre abrégé: Front Mol Neurosci
Pays: Switzerland
ID NLM: 101477914

Informations de publication

Date de publication:
2020
Historique:
received: 29 08 2019
accepted: 12 02 2020
entrez: 16 4 2020
pubmed: 16 4 2020
medline: 16 4 2020
Statut: epublish

Résumé

Stroke is the leading cause of morbidity and mortality worldwide. About 87% of stroke cases are ischemic, which disrupt the physiological activity of the brain, thus leading to a series of complex pathophysiological events. Despite decades of research on neuroprotectants to probe for suitable therapies against ischemic stroke, no successful results have been obtained, and new alternative approaches are urgently required in order to combat this pathological torment. To address these problems, drug repositioning/reprofiling is explored extensively. Drug repurposing aims to identify new uses for already established drugs, and this makes it an attractive commercial strategy. Nuclear factor-kappa beta (NF-κB) is reported to be involved in many physiological and pathological conditions, such as neurodegeneration, neuroinflammation, and ischemia/reperfusion (I/R) injury. In this study, we examined the neuroprotective effects of atorvastatin, cephalexin, and mycophenolate against the NF-κB in ischemic stroke, as compared to the standard NF-κB inhibitor caeffic acid phenethyl ester (CAPE). An in-silico docking analysis was performed and their potential neuroprotective activities in the

Identifiants

pubmed: 32292329
doi: 10.3389/fnmol.2020.00033
pmc: PMC7121334
doi:

Types de publication

Journal Article Retracted Publication

Langues

eng

Pagination

33

Commentaires et corrections

Type : RetractionIn

Informations de copyright

Copyright © 2020 Ali, Shah, Zeb, Malik, Alvi, Alkury, Rashid, Hussain, Ullah, Ullah Khan, Koh and Li.

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Auteurs

Awais Ali (A)

Riphah Institute of Pharmaceutical Sciences, Riphah International University, Islamabad, Pakistan.

Fawad Ali Shah (FA)

Riphah Institute of Pharmaceutical Sciences, Riphah International University, Islamabad, Pakistan.

Alam Zeb (A)

Riphah Institute of Pharmaceutical Sciences, Riphah International University, Islamabad, Pakistan.

Imran Malik (I)

Riphah Institute of Pharmaceutical Sciences, Riphah International University, Islamabad, Pakistan.

Arooj Mohsin Alvi (AM)

Riphah Institute of Pharmaceutical Sciences, Riphah International University, Islamabad, Pakistan.

Lina Tariq Alkury (LT)

College of Natural and Health Sciences, Zayed University, Abu Dhabi, United Arab Emirates.

Sajid Rashid (S)

National Center for Bioinformatics, Quaid-i-Azam University, Islamabad, Pakistan.

Ishtiaq Hussain (I)

Department of Pharmacy, Abbottabad University of Science and Technology, Khyber Pakhtunkhwa, Pakistan.

Najeeb Ullah (N)

Institute of Basic Medical Sciences, Khyber Medical University, Peshawar, Pakistan.
State Key Laboratory of Oncogenomics, School of Chemical Biology and Biotechnology, Peking University Shenzhen, China.

Arif Ullah Khan (AU)

Riphah Institute of Pharmaceutical Sciences, Riphah International University, Islamabad, Pakistan.

Phil Ok Koh (PO)

Department of Anatomy, College of Veterinary Medicine, Research Institute of Life Science, Gyeongsang National University, Jinju, South Korea.

Shupeng Li (S)

State Key Laboratory of Oncogenomics, School of Chemical Biology and Biotechnology, Peking University Shenzhen, China.
Centre for Addiction and Mental Health, Campbell Research Institute, Toronto, ON, Canada.

Classifications MeSH