Wnt and GSK3 Signaling Pathways in Bipolar Disorder: Clinical and Therapeutic Implications

被引:53
|
作者
Muneer, Ather [1 ]
机构
[1] Riphah Int Univ, Islamic Int Med Coll, Dept Psychiat, 274 Peshawar Rd, Rawalpindi, Pakistan
关键词
Bipolar disorder; Glycogen synthase kinase 3; Wnt; Protein kinase B; beta-catenin; Canonical Wnt pathway; GLYCOGEN-SYNTHASE KINASE-3; ADULT HIPPOCAMPAL NEUROGENESIS; BETA-CATENIN; MOOD DISORDERS; CIRCADIAN RHYTHMICITY; STEM-CELLS; LITHIUM; MODELS; MICE; DYSREGULATION;
D O I
10.9758/cpn.2017.15.2.100
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The neurobiology of bipolar disorder, a chronic and systemic ailment is not completely understood. The bipolar phenotype manifests in myriad ways, and psychopharmacological agents like lithium have long term beneficial effects. The enzyme glycogen synthase kinase 3 (GSK3) has come into focus, as lithium and several other mood stabilizing medications inhibit its activity. This kinase and its key upstream modulator, Wnt are dysregulated in mood disorders and there is a growing impetus to delineate the chief substrates involved in the development of these illnesses. In May 2016, a comprehensive literature search was undertaken which revealed that there is over activity of GSK3 in bipolar disorder with deleterious downstream effects like proinflammatory status, increased oxidative stress, and circadian dysregulation leading to declining neurotrophic support and enhanced apoptosis of neural elements. By developing specific GSK3 inhibitors the progressive worsening in bipolar disorder can be forestalled with improved prospects for the sufferers.
引用
收藏
页码:100 / 114
页数:15
相关论文
共 50 条
  • [1] An emerging role for Wnt and GSK3 signaling pathways in schizophrenia
    Singh, K. K.
    CLINICAL GENETICS, 2013, 83 (06) : 511 - 517
  • [2] GSK-3 and Wnt signaling in neurogenesis and bipolar disorder
    Valvezan, Alexander J.
    Klein, Peter S.
    FRONTIERS IN MOLECULAR NEUROSCIENCE, 2012, 5
  • [3] GSK3: a multifaceted kinase in Wnt signaling
    Wu, Dianqing
    Pan, Weijun
    TRENDS IN BIOCHEMICAL SCIENCES, 2010, 35 (03) : 161 - 168
  • [4] Synaptic Wnt/GSK3β Signaling Hub in Autism
    Caracci, Mario O.
    Avila, Miguel E.
    De Ferrari, Giancarlo V.
    NEURAL PLASTICITY, 2016, 2016
  • [5] Inositol depletion, GSK3 inhibition and bipolar disorder
    Yu, Wenxi
    Greenberg, Miriam L.
    FUTURE NEUROLOGY, 2016, 11 (02) : 135 - 148
  • [6] Cross-talk of WNT and FGF signaling pathways at GSK3β to regulate β-catenin and SNAIL signaling cascades
    Katoh, Masuko
    Katoh, Masaru
    CANCER BIOLOGY & THERAPY, 2006, 5 (09) : 1059 - 1064
  • [7] Wnt Signaling: Multivesicular Bodies Hold GSK3 Captive
    Niehrs, Christof
    Acebron, Sergio P.
    CELL, 2010, 143 (07) : 1044 - 1046
  • [8] Targeting GSK3 and Associated Signaling Pathways Involved in Cancer
    Duda, Przemyslaw
    Akula, Shaw M.
    Abrams, Stephen L.
    Steelman, Linda S.
    Martelli, Alberto M.
    Cocco, Lucio
    Ratti, Stefano
    Candido, Saverio
    Libra, Massimo
    Montalto, Giuseppe
    Cervello, Melchiorre
    Gizak, Agnieszka
    Rakus, Dariusz
    McCubrey, James A.
    CELLS, 2020, 9 (05)
  • [9] Exploring the wnt and notch signaling pathways in schizophrenia and bipolar disorder
    Hoseth, E. Z.
    Dieset, I.
    Ragni, M.
    Sigrun, H.
    Tove, L.
    Aurelija, A.
    Annika, M.
    Ingrid, M.
    Pal, A.
    Srdjan, D.
    Ole, A. A.
    Thor, U.
    BIPOLAR DISORDERS, 2017, 19 : 123 - 123
  • [10] Inhibition of GSK3 and MEK induced cancer stem cell generation via the Wnt and MEK signaling pathways
    Liao, Shengtao
    Gan, Li
    Qin, Wanxiang
    Liu, Chang
    Mei, Zhechuan
    ONCOLOGY REPORTS, 2018, 40 (04) : 2005 - 2013