Glycogen Synthase Kinase-3 as a Therapeutic Target for Cognitive Dysfunction in Neuropsychiatric Disorders

被引:54
作者
O'Leary, Olivia [1 ]
Nolan, Yvonne [1 ]
机构
[1] Natl Univ Ireland Univ Coll Cork, Dept Anat & Neurosci, Cork, Ireland
基金
爱尔兰科学基金会;
关键词
AMYLOID PROTEIN DEPOSITION; POSTMORTEM FRONTAL-CORTEX; EUTHYMIC BIPOLAR PATIENTS; LONG-TERM POTENTIATION; ALZHEIMERS-DISEASE; LITHIUM TREATMENT; BETA-CATENIN; TAU PHOSPHORYLATION; PREFRONTAL CORTEX; TRANSGENIC MODEL;
D O I
10.1007/s40263-014-0213-z
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The serine/threonine kinase glycogen synthase kinase-3 (GSK-3) is involved in a broad range of cellular processes including cell proliferation, apoptosis and inflammation. It is now also increasingly acknowledged as having a role to play in cognitive-related processes such as neurogenesis, synaptic plasticity and neural cell survival. Cognitive impairment represents a major debilitating feature of many neurodegenerative and psychiatric disorders, including Alzheimer's disease, mood disorders, schizophrenia and fragile X syndrome, as well as being a result of traumatic brain injury or cranial irradiation. Accordingly, GSK-3 has been identified as an important therapeutic target for cognitive impairment, and recent preclinical studies have yielded important evidence demonstrating that GSK-3 inhibitors may be useful therapeutic interventions for restoring cognitive function in some of these brain disorders. The current review summarises the role of GSK-3 as a regulator of cognitive-dependent functions, examines current preclinical and clinical evidence of the potential of GSK-3 inhibitors as therapeutic agents for cognitive impairments in neuropsychiatric disorders, and offers some insight into the current obstacles that are impeding the clinical use of selective GSK-3 inhibitors in the treatment of cognitive impairment.
引用
收藏
页码:1 / 15
页数:15
相关论文
共 190 条
[1]   Antipsychotics alter the protein expression levels of β-catenin and GSK-3 in the rat medial prefrontal cortex and striatum [J].
Alimohamad, H ;
Rajakumar, N ;
Seah, YH ;
Rushlow, W .
BIOLOGICAL PSYCHIATRY, 2005, 57 (05) :533-542
[2]   Neurocognitive function in clinically stable men with bipolar I disorder or schizophrenia and normal control subjects [J].
Altshuler, LL ;
Ventura, J ;
van Gorp, WG ;
Green, MF ;
Theberge, DC ;
Mintz, J .
BIOLOGICAL PSYCHIATRY, 2004, 56 (08) :560-569
[3]  
Aplin AE, 1996, J NEUROCHEM, V67, P699
[4]   Inhibition of Glycogen Synthase Kinase-3 Ameliorates β-Amyloid Pathology and Restores Lysosomal Acidification and Mammalian Target of Rapamycin Activity in the Alzheimer Disease Mouse Model [J].
Avrahami, Limor ;
Farfara, Dorit ;
Shaham-Kol, Maya ;
Vassar, Robert ;
Frenkel, Dan ;
Eldar-Finkelman, Hagit .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2013, 288 (02) :1295-1306
[5]   Glycogen synthase kinase-3β immunoreactivity is reduced in the prefrontal cortex in schizophrenia [J].
Beasley, C ;
Cotter, D ;
Khan, N ;
Pollard, C ;
Sheppard, P ;
Varndell, I ;
Lovestone, S ;
Anderton, B ;
Everall, I .
NEUROSCIENCE LETTERS, 2001, 302 (2-3) :117-120
[6]   Role of GSK3β in behavioral abnormalities induced by serotonin deficiency [J].
Beaulieu, Jean-Martin ;
Zhang, Xiaodong ;
Rodriguiz, Ramona M. ;
Sotnikova, Tatyana D. ;
Cools, Michael J. ;
Wetsel, William C. ;
Gainetdinov, Raul R. ;
Caron, Marc G. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (04) :1333-1338
[7]   A role for Akt and glycogen synthase kinase-3 as integrators of dopamine and serotonin neurotransmission in mental health [J].
Beaulieu, Jean-Martin .
JOURNAL OF PSYCHIATRY & NEUROSCIENCE, 2012, 37 (01) :7-16
[8]   Lithium antagonizes dopamine-dependent behaviors mediated by an AKT/glycogen synthase kinase 3 signaling cascade [J].
Beaulieu, JM ;
Sotnikova, TD ;
Yao, WD ;
Kockeritz, L ;
Woodgett, JR ;
Gainetdinov, RR ;
Caron, MG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (14) :5099-5104
[9]   An Akt/β-arrestin 2/PP2A signaling complex mediates dopaminergic neurotransmission and behavior [J].
Beaulieu, JM ;
Sotnikova, TD ;
Marion, S ;
Lefkowitz, RJ ;
Gainetdinov, RR ;
Caron, MG .
CELL, 2005, 122 (02) :261-273
[10]   Long-term response to lithium salts in bipolar illness is influenced by the glycogen synthase kinase 3-β -50 T/C SNP [J].
Benedetti, F ;
Serretti, A ;
Pontiggia, A ;
Bernasconi, A ;
Lorenzi, C ;
Colombo, C ;
Smeraldi, E .
NEUROSCIENCE LETTERS, 2005, 376 (01) :51-55