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Published Online: 1 November 2004

Neural and Endocrine Correlates of Sadness In Women: Implications for Neural Network Regulation of HPA Activity

Publication: The Journal of Neuropsychiatry and Clinical Neurosciences

Abstract

In order to evaluate the suprahypothalamic neuroanatomical sites of relevance to adrenocorticotropic hormone (ACTH) and cortisol regulation, single photon emission computed tomography (SPECT) investigation of induced sadness was combined with a linear regression analysis of these hormone levels during mood induction. Images from eight healthy women were analyzed by statistical parametric mapping (SPM), replicating many findings from prior sadness induction studies. Statistical parametric mapping endocrine covariate analysis showed that the ventromedial prefrontal, anterior cingulate, and insular cortices may regulate ACTH and the insular cortex may be related to regulation of cortisol during sadness. Dysfunction of these sites may contribute to the cortisol dysregulation observed in some subjects with major depression.

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Published In

Go to The Journal of Neuropsychiatry and Clinical Neurosciences
Go to The Journal of Neuropsychiatry and Clinical Neurosciences
The Journal of Neuropsychiatry and Clinical Neurosciences
Pages: 446 - 455
PubMed: 15616171

History

Published online: 1 November 2004
Published in print: November 2004

Authors

Details

William E. Ottowitz, M.D.
Received August 8, 2002; revised February 24, 2003, accepted March 11, 2003. From the Department of Nuclear Medicine, St. Elizabeth’s Hospital, Boston Massachusetts. Address correspondence to Dr. Ottowitz, Massachusetts General Hospital, Psychiatric Neuroscience Program, Building 149, 2nd floor, 13th St., Charlestown, MA 02129; [email protected] (E-mail).
Darin D. Dougherty, M.D.
Received August 8, 2002; revised February 24, 2003, accepted March 11, 2003. From the Department of Nuclear Medicine, St. Elizabeth’s Hospital, Boston Massachusetts. Address correspondence to Dr. Ottowitz, Massachusetts General Hospital, Psychiatric Neuroscience Program, Building 149, 2nd floor, 13th St., Charlestown, MA 02129; [email protected] (E-mail).
Alan Sirota, Ph.D.
Received August 8, 2002; revised February 24, 2003, accepted March 11, 2003. From the Department of Nuclear Medicine, St. Elizabeth’s Hospital, Boston Massachusetts. Address correspondence to Dr. Ottowitz, Massachusetts General Hospital, Psychiatric Neuroscience Program, Building 149, 2nd floor, 13th St., Charlestown, MA 02129; [email protected] (E-mail).
Raymond Niaura, Ph.D.
Received August 8, 2002; revised February 24, 2003, accepted March 11, 2003. From the Department of Nuclear Medicine, St. Elizabeth’s Hospital, Boston Massachusetts. Address correspondence to Dr. Ottowitz, Massachusetts General Hospital, Psychiatric Neuroscience Program, Building 149, 2nd floor, 13th St., Charlestown, MA 02129; [email protected] (E-mail).
Scott L. Rauch, M.D.
Received August 8, 2002; revised February 24, 2003, accepted March 11, 2003. From the Department of Nuclear Medicine, St. Elizabeth’s Hospital, Boston Massachusetts. Address correspondence to Dr. Ottowitz, Massachusetts General Hospital, Psychiatric Neuroscience Program, Building 149, 2nd floor, 13th St., Charlestown, MA 02129; [email protected] (E-mail).
Walter A. Brown, M.D.
Received August 8, 2002; revised February 24, 2003, accepted March 11, 2003. From the Department of Nuclear Medicine, St. Elizabeth’s Hospital, Boston Massachusetts. Address correspondence to Dr. Ottowitz, Massachusetts General Hospital, Psychiatric Neuroscience Program, Building 149, 2nd floor, 13th St., Charlestown, MA 02129; [email protected] (E-mail).

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