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The Role of Glycogen Synthase Kinase 3 Beta in Multiple Sclerosis Publisher Pubmed



Noori T1 ; Dehpour AR2, 3 ; Sureda A4 ; Fakhri S1 ; Sobarzosanchez E5, 6 ; Farzaei MH1 ; Kupeli Akkol E7 ; Khodarahmi Z8 ; Hosseini SZ8 ; Alavi SD8 ; Shirooie S1
Authors
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Authors Affiliations
  1. 1. Pharmaceutical Sciences Research Center, Health Institute, Kermanshah University of Medical Sciences, Kermanshah, 6734667149, Iran
  2. 2. Department of Pharmacology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
  3. 3. Experimental Medicine Research Center, TUMS, Tehran, Iran
  4. 4. Research Group on Community Nutrition and Oxidative Stress (NUCOX) and CIBEROBN (Physiopathology of Obesity and Nutrition CB12/03/30038), University of Balearic Islands, Palma de Mallorca E-07122, Balearic Islands, Spain
  5. 5. Instituto de Investigacion e Innovacion en Salud, Facultad de Ciencias de la Salud, Universidad Central de Chile, Chile
  6. 6. Department of Organic Chemistry, Faculty of Pharmacy, University of Santiago de Compostela, Spain
  7. 7. Department of Pharmacognosy, Faculty of Pharmacy, Gazi University, Etiler, Ankara, 06330, Turkey
  8. 8. Student Research Committee, Faculty of Pharmacy, Kermanshah University of Medical Sciences, Kermanshah, 6714415153, Iran

Source: Biomedicine and Pharmacotherapy Published:2020


Abstract

Multiple sclerosis (MS) is an autoimmune disease of the central nervous system (CNS) that leads to progressive neurological disability due to axonal deterioration. Although MS presents profound heterogeneity in the clinical course, its underlying central mechanism is active demyelination and neurodegeneration associated with inflammation. Multiple autoimmune and neuroinflammatory pathways are involved in the demyelination process of MS. Analysis of MS lesions has shown that inflammatory genes are upregulated. Glycogen synthase kinase-3 (GSK-3) is part of the mitogen-activated protein kinase (MAPK) family and has important roles in many signaling cascades. GSK-3 is a highly conserved serine/threonine protein kinase expressed in both the central and the peripheral nervous systems. GSK-3 modulates several biological processes through phosphorylation of protein kinases, including cell signaling, neuronal growth, apoptosis and production of pro-inflammatory cytokines and interleukins, allowing adaptive changes in events such as cellular proliferation, migration, inflammation, and immunity. GSK-3 occurs in mammals in two isoforms GSK-3α and GSK-3β, both of which are common in the brain, although GSK-3α is found particularly in the cerebral cortex, cerebellum, striated hippocampus and Purkinje cells, while GSK-3β is found in all brain regions. In patients with chronic progressive MS, expression of GSK-3β is elevated in several brain regions such as the corpus callosum and cerebral cortex. GSK-3β inhibition may play a role in glial cell activation, reducing pathological pain induced by nerve injury by formalin injection. According to the role of GSK-3β in pathological conditions, the aim of this article is review of the role of GSK-3β in multiple sclerosis and inflammation of neurons. © 2020 The Authors