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Convergent Effects of Acute Stress and Glucocorticoid Exposure upon MAO-A in Humans

Convergent Effects of Acute Stress and Glucocorticoid Exposure upon MAO-A in Humans

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SOLIMAN, Alexandra, Chinelo UDEMGBA, Ian FAN, Xin XU, Laura MILER, Pablo RUSJAN, Sylvain HOULE, Alan A. WILSON, Jens PRUESSNER, Jeffrey H. MEYER, 2012. Convergent Effects of Acute Stress and Glucocorticoid Exposure upon MAO-A in Humans. In: Journal of Neuroscience. 32(48), pp. 17120-17127. ISSN 0270-6474. eISSN 1529-2401. Available under: doi: 10.1523/JNEUROSCI.2091-12.2012

@article{Soliman2012-11-28Conve-38386, title={Convergent Effects of Acute Stress and Glucocorticoid Exposure upon MAO-A in Humans}, year={2012}, doi={10.1523/JNEUROSCI.2091-12.2012}, number={48}, volume={32}, issn={0270-6474}, journal={Journal of Neuroscience}, pages={17120--17127}, author={Soliman, Alexandra and Udemgba, Chinelo and Fan, Ian and Xu, Xin and Miler, Laura and Rusjan, Pablo and Houle, Sylvain and Wilson, Alan A. and Pruessner, Jens and Meyer, Jeffrey H.} }

Miler, Laura Soliman, Alexandra Rusjan, Pablo Miler, Laura Convergent Effects of Acute Stress and Glucocorticoid Exposure upon MAO-A in Humans Soliman, Alexandra Meyer, Jeffrey H. Xu, Xin Wilson, Alan A. Udemgba, Chinelo Pruessner, Jens Houle, Sylvain Pruessner, Jens Fan, Ian Monoamine oxidase-A (MAO-A), a key brain enzyme which metabolizes monoamines, is implicated in the pathophysiology of stress-related illnesses, including major depressive disorder, addiction, and violent behavior. Chronic stressors and glucocorticoid-administration typically associate with elevated MAO-A levels/activity. However, the relationship of shorter stress or glucocorticoid exposures and MAO-A levels/activity is not well established. Our objectives are to assess effects of acute stress upon MAO-A V<sub>T,</sub> an index of MAO-A density, in human brain and acute glucocorticoid exposure upon MAO-A levels in human neuronal and glial cell lines. Twelve healthy, non-smoking participants aged 18-50 underwent [<sup>11</sup>C]harmine positron emission tomography to measure brain MAO-A V<sub>T</sub> on two different days: One under acute psychosocial stress (via Trier Social Stress and Montreal Imaging Stress Tasks) and one under a non-stress condition. MAO-A density (by Western blot) and activity (by [<sup>14</sup>C]-5-HT metabolism and liquid scintillation spectroscopy) were measured in human neuronal and glial cell lines after 4 h exposure to dexamethasone. We observed a significant reduction in whole-brain MAO-A binding as reflected by reductions in 10 of 11 brain regions. Acute dexamethasone exposure in neuronal and glial cells significantly decreased MAO-A activity and protein levels. We observed a highly consistent relationship between acute stressors and glucocorticoid administration and decreased MAO-A binding, activity and protein levels. Since MAO-A metabolizes monoamines, this phenomenon may explain why acute stressors benefit healthy animals even though chronic stress is associated with illness. Rusjan, Pablo Udemgba, Chinelo Houle, Sylvain Wilson, Alan A. eng Fan, Ian Meyer, Jeffrey H. 2012-11-28 Xu, Xin 2017-04-06T11:08:42Z 2017-04-06T11:08:42Z

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