2009
DOI: 10.1016/s1734-1140(09)70113-6
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Prenatal stress decreases glycogen synthase kinase-3 phosphorylation in the rat frontal cortex

Abstract: It has been postulated that hyperactive glycogen synthase kinase-3 (GSK-3) is an important factor in the pathogenesis of depression, and that this enzyme also contributes to the mechanism of antidepressant drug action. In the present study, we investigated the effect of prenatal stress (an animal model of depression) and long-term treatment with antidepressant drugs on the concentration of GSK-3beta and its main regulating protein kinase B (PKB, Akt). The concentration of GSK-3beta, its inactive form (phospho-… Show more

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Cited by 31 publications
(27 citation statements)
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“…Prenatal stress is one of the well-characterized animal models of depression, and the face, predictive and construct validities of this model have previously been reported [8,25,28,29,32,33,34]. In addition to depression-like behavioral changes, hyperactivity of the HPA axis and increases in blood glucose levels were observed in this model.…”
Section: Discussionmentioning
confidence: 58%
“…Prenatal stress is one of the well-characterized animal models of depression, and the face, predictive and construct validities of this model have previously been reported [8,25,28,29,32,33,34]. In addition to depression-like behavioral changes, hyperactivity of the HPA axis and increases in blood glucose levels were observed in this model.…”
Section: Discussionmentioning
confidence: 58%
“…Mice overexpressing GSK-3β shows prodepressant-like phenotype and increased sensitivity to chronic mild stress; these behaviour changes can be prevented by chronic, but not by acute treatment with fluoxetine (Zhang et al 2013). In prenatally stressed rats GSK-3β levels were significantly elevated in the frontal cortex, but not in the hippocampus (Szymańska et al 2009), while concentration of phosphorylated GSK-3β was decreased only in the former structure. Chronic treatment with antidepressant drugs diminished stress-induced alterations in GSK-3β and phospho-GSK-3β only in the frontal cortex (Szymańska et al 2009).…”
Section: Discussionmentioning
confidence: 94%
“…In prenatally stressed rats GSK-3β levels were significantly elevated in the frontal cortex, but not in the hippocampus (Szymańska et al 2009), while concentration of phosphorylated GSK-3β was decreased only in the former structure. Chronic treatment with antidepressant drugs diminished stress-induced alterations in GSK-3β and phospho-GSK-3β only in the frontal cortex (Szymańska et al 2009). In addition, chronic treatment with citalopram alleviated the depression-like behaviors and reversed the decrease of the phosphorylated GSK-3β in stressed rats (Liu et al 2012).…”
Section: Discussionmentioning
confidence: 94%
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“…Patients with schizophrenia spectrum had a larger pituitary volume (larger in female than male patients), reflecting hyperactivity of the HPA axis, which may be related to a common vulnerability to stress in patients [63]. Dysregulation of HPA axis activity can be detected not only in depressed but also in schizophrenic patients [64,65], and the hypothesis of HPA axis hyperactivity in schizophrenia was supported by an experiment using a neurodevelopmental model of schizophrenia in rats [66]. HPA axis activity is associated with the severity of multiple types of symptoms in first-episode psychosis, and patients' diagnosis and clinical phase partially influence these associations [67].…”
Section: Hypothalamusmentioning
confidence: 99%