4 results match your criteria: "Massachusetts General Hospital and Massachusetts Institute of Technology[Affiliation]"
Biol Psychiatry
April 2015
Department of Psychiatry, Harvard Medical School, Boston; Connors Center for Women's Health and Gender Biology, Division of Women's Health, Department of Medicine, Brigham & Women's Hospital, Boston; Department of Psychiatry, Brigham & Women's Hospital, Boston; Athinoula A. Martinos Center, Massachusetts General Hospital and Massachusetts Institute of Technology, Charlestown, Massachusetts.. Electronic address:
Biol Psychiatry
July 2015
Center for Depression, Anxiety and Stress Research, McLean Hospital, Belmont, Massachusetts; McLean Imaging Center, McLean Hospital, Belmont, Massachusetts; Department of Psychiatry, Harvard Medical School, Cambridge, Massachusetts. Electronic address:
Background: Increased sensitivity to stress and dysfunctional reward processing are two primary characteristics of major depressive disorder (MDD) that may persist after remission. Preclinical work has established the pivotal role of the striatum in mediating both stress and reward responses. Human neuroimaging studies have corroborated these preclinical findings and highlighted striatal dysfunction in MDD in response to reward but have yet to investigate striatal function during stress, in particular in individuals with recurrent depression.
View Article and Find Full Text PDFNeuropsychopharmacology
February 2015
1] Division of Women's Health, Department of Medicine, Brigham and Women's Hospital, Boston, MA, USA [2] Department of Psychiatry, Brigham and Women's Hospital, Boston, MA, USA [3] Harvard Medical School, Boston, MA, USA [4] Athinoula A. Martinos Center, Massachusetts General Hospital and Massachusetts Institute of Technology, Charlestown, MA, USA.
Many regions within stress neurocircuitry, including the anterior hypothalamus, amygdala, hippocampus, and medial prefrontal cortex, are densely populated with sex steroid receptors. Substantial evidence from animal studies indicates that the gonadal hormone 17β-estradiol (E₂) impacts the structure and function of these regions, but human studies are limited. Characterizing estradiol's role in stress circuitry in vivo in humans may have important clinical implications given the comorbidity between major depressive disorder (MDD), stress circuitry dysfunction and endocrine dysregulation.
View Article and Find Full Text PDFPsychiatry Res
August 2014
Division of Women׳s Health, Department of Medicine, Boston, MA, USA; Department of Psychiatry, Brigham & Women׳s Hospital, Boston, MA, USA; Harvard Medical School, Boston, MA, USA; Athinoula A. Martinos Center, Massachusetts General Hospital and Massachusetts Institute of Technology, Charlestown, MA, USA.
Evidence contributing to the understanding of neurobiological mechanisms underlying appetite dysregulation in anorexia nervosa draws heavily on separate lines of research into neuroendocrine and neural circuitry functioning. In particular, studies consistently cite elevated ghrelin and abnormal activation patterns in homeostatic (hypothalamus) and hedonic (striatum, amygdala, insula) regions governing appetite. The current preliminary study examined the interaction of these systems, based on research demonstrating associations between circulating ghrelin levels and activity in these regions in healthy individuals.
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