Monoamine Oxidase A is Required for Rapid Dendritic Remodeling in Response to Stress
Author(s) -
Sean C. Godar,
Marco Bortolato,
S. Richards,
Felix G. Li,
Kai Chen,
Cara L. Wellman,
Jean C. Shih
Publication year - 2015
Publication title -
the international journal of neuropsychopharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.897
H-Index - 107
eISSN - 1469-5111
pISSN - 1461-1457
DOI - 10.1093/ijnp/pyv035
Subject(s) - monoamine neurotransmitter , monoamine oxidase , basolateral amygdala , dendritic spine , neuroscience , amygdala , psychology , serotonin , chemistry , enzyme , biochemistry , hippocampal formation , receptor
Acute stress triggers transient alterations in the synaptic release and metabolism of brain monoamine neurotransmitters. These rapid changes are essential to activate neuroplastic processes aimed at the appraisal of the stressor and enactment of commensurate defensive behaviors. Threat evaluation has been recently associated with the dendritic morphology of pyramidal cells in the orbitofrontal cortex (OFC) and basolateral amygdala (BLA); thus, we examined the rapid effects of restraint stress on anxiety-like behavior and dendritic morphology in the BLA and OFC of mice. Furthermore, we tested whether these processes may be affected by deficiency of monoamine oxidase A (MAO-A), the primary enzyme catalyzing monoamine metabolism.
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