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CNS Neurosci Ther ; 21(5): 398-409, 2015 May.
Article in English | MEDLINE | ID: mdl-25611431

ABSTRACT

AIMS: This study explored whether surgical stress-induced glucocorticoid receptor (GR) phosphorylation is related to postoperative cognitive dysfunction (POCD) in aged individuals. Inhibition of GR activation could be an effective treatment for POCD. METHODS: A laparotomy was given to C57/BL6 mice in POCD group both 20 and 6 months old. Animals in control group were treated in identical manners except for laparotomy. Cognitive function was evaluated by Morris water maze and elevated plus maze. Western blot and Elisa assay were used to detect related molecules. Mifepristone and roscovitine were treated as inhibitions of GR phosphorylation. RESULTS: The cognitive function was impaired, and brain-derived neurotrophic factor (BDNF) was found reduced in aged POCD group. GR translocation into nucleus and elevated GR phosphorylation were found in prefrontal cortex of aged POCD mice. Cyclin-dependent Kinase 5 (CDK5), kinase for GR phosphorylation also elevated in aged POCD mice. With GR antagonist and CDK5 inhibitor, reduction of BDNF and cognitive dysfunction in aged mice were both rescued. CONCLUSION: These results presented a mechanism that surgical stress-induced GR phosphorylation contributes to POCD in aged individuals. Inhibition of GR activation and phosphorylation might be a potential treatment target of POCD.


Subject(s)
Brain-Derived Neurotrophic Factor/deficiency , Cognition Disorders/metabolism , Postoperative Complications/metabolism , Prefrontal Cortex/metabolism , Receptors, Glucocorticoid/metabolism , Stress, Physiological/physiology , Active Transport, Cell Nucleus/physiology , Aging/metabolism , Animals , Cognition Disorders/etiology , Cyclin-Dependent Kinase 5/antagonists & inhibitors , Cyclin-Dependent Kinase 5/metabolism , Disease Models, Animal , Laparotomy/adverse effects , Male , Maze Learning/drug effects , Maze Learning/physiology , Mice, Inbred C57BL , Phosphorylation/drug effects , Postoperative Complications/psychology , Prefrontal Cortex/drug effects , Receptors, Glucocorticoid/antagonists & inhibitors
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