Literature DB >> 23916593

Glycogen synthase kinase-3 inhibitors: Rescuers of cognitive impairments.

Margaret K King1, Marta Pardo1, Yuyan Cheng1, Kimberlee Downey1, Richard S Jope1, Eléonore Beurel2.   

Abstract

Impairment of cognitive processes is a devastating outcome of many diseases, injuries, and drugs affecting the central nervous system (CNS). Most often, very little can be done by available therapeutic interventions to improve cognitive functions. Here we review evidence that inhibition of glycogen synthase kinase-3 (GSK3) ameliorates cognitive deficits in a wide variety of animal models of CNS diseases, including Alzheimer's disease, Fragile X syndrome, Down syndrome, Parkinson's disease, spinocerebellar ataxia type 1, traumatic brain injury, and others. GSK3 inhibitors also improve cognition following impairments caused by therapeutic interventions, such as cranial irradiation for brain tumors. These findings demonstrate that GSK3 inhibitors are able to ameliorate cognitive impairments caused by a diverse array of diseases, injury, and treatments. The improvements in impaired cognition instilled by administration of GSK3 inhibitors appear to involve a variety of different mechanisms, such as supporting long-term potentiation and diminishing long-term depression, promotion of neurogenesis, reduction of inflammation, and increasing a number of neuroprotective mechanisms. The potential for GSK3 inhibitors to repair cognitive deficits associated with many conditions warrants further investigation of their potential for therapeutic interventions, particularly considering the current dearth of treatments available to reduce loss of cognitive functions.
© 2013.

Entities:  

Keywords:  1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine; AD; APP; Alzheimer's disease; Aβ; CNS; FX; Fragile X; Fragile X syndrome; GSK3; Glycogen synthase kinase-3; LTD; LTP; Learning; Lithium; MTPT; SCA1; TBI; amyloid precursor protein; amyloid-β peptide; central nervous system; glycogen synthase kinase-3; long-term depression; long-term potentiation; spinocerebellar ataxia type 1; traumatic brain injury

Mesh:

Substances:

Year:  2013        PMID: 23916593      PMCID: PMC3867580          DOI: 10.1016/j.pharmthera.2013.07.010

Source DB:  PubMed          Journal:  Pharmacol Ther        ISSN: 0163-7258            Impact factor:   12.310


  203 in total

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