Wnt and GSK3 Signaling Pathways in Bipolar Disorder: Clinical and Therapeutic Implications
Clinical Psychopharmacology and Neuroscience
;
: 100-114, 2017.
Artigo
em Inglês
| WPRIM
| ID: wpr-203972
ABSTRACT
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.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Fenótipo
/
Fosfotransferases
/
Transtorno Bipolar
/
Neurobiologia
/
Apoptose
/
Estresse Oxidativo
/
Transtornos do Humor
/
Transtornos Cronobiológicos
/
Quinase 3 da Glicogênio Sintase
/
Proteínas Proto-Oncogênicas c-akt
Idioma:
Inglês
Revista:
Clinical Psychopharmacology and Neuroscience
Ano de publicação:
2017
Tipo de documento:
Artigo
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