Panic Disorder affects roughly 1-2% of the general population with more women than men affected. Although drug and behavioral treatments are relatively effective in treating this disorder, its etiology and pathophysiology remain poorly understood. Pharmacological challenges and treatment in humans have helped define panic disorder, but ethical and practical constraints limit scientific exploration. We propose further neurochemical and behavioral investigation of the provocation of anxiety symptoms in nonhuman primates which reliably mirror significant aspects of human panic response. We have labeled these symptoms, """"""""Acute Endogenous Distress"""""""" (AED). The proposed work will examine the hypothesized central role of the locus ceruleus in mediating these acute anxiety responses and the possible role of dysregulation of several neurochemical systems in modulating LC responsivity. These experiments will employ agents capable of provoking panic in patients which we have previously demonstrated as effective in primates, particularly sodium lactate and yohimbine. Our goals include determination of the role of centrally administered CRF, the effects of serotonin and its depletion, and the possible role of Glutamate in the pathophysiology of AED. Comparisons of pre- and post-treatment CSF levels of major neurotransmitters and cardiac responsivity during AED provocation will permit assessment of baseline and altered neurochemical status on AED susceptibility. In addition to the pharmacological probes, our primate studies will allow us to examine developmentally the hypothesized role of early attachment/mastery experience in the emergence of AED and its neurochemical underpinnings. The effects of recent stressful events, which have been linked theoretically to panic vulnerability in humans, will also be studied. Systematic observations of a range of previously defined anxiety patterns form the core of the AED assessments, while the possible cognitive effects of AED will employ novel computer-based video tasks of varying difficulty. The use of primates in the systematic examination of hypotheses which have emerged from the human literature, but which remain untestable at the human level, is critical to our understanding and ultimate treatment of panic disorder.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
5R01MH042545-06
Application #
2245474
Study Section
Special Emphasis Panel (SRCM)
Project Start
1988-02-01
Project End
1998-08-31
Budget Start
1995-09-01
Budget End
1996-08-31
Support Year
6
Fiscal Year
1995
Total Cost
Indirect Cost
Name
Suny Downstate Medical Center
Department
Psychiatry
Type
Schools of Medicine
DUNS #
068552207
City
Brooklyn
State
NY
Country
United States
Zip Code
11203
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Smith, Eric L P; Batuman, Olcay A; Trost, Ronald C et al. (2002) Transforming growth factor-beta 1 and cortisol in differentially reared primates. Brain Behav Immun 16:140-9
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Smith, E L; Coplan, J D; Trost, R C et al. (1997) Neurobiological alterations in adult nonhuman primates exposed to unpredictable early rearing. Relevance to posttraumatic stress disorder. Ann N Y Acad Sci 821:545-8
Trappler, B; Friedman, S (1996) Posttraumatic stress disorder in survivors of the Brooklyn Bridge shooting. Am J Psychiatry 153:705-7
Coplan, J D; Andrews, M W; Rosenblum, L A et al. (1996) Persistent elevations of cerebrospinal fluid concentrations of corticotropin-releasing factor in adult nonhuman primates exposed to early-life stressors: implications for the pathophysiology of mood and anxiety disorders. Proc Natl Acad Sci U S A 93:1619-23
Coplan, J D; Rosenblum, L A; Gorman, J M (1995) Primate models of anxiety. Longitudinal perspectives. Psychiatr Clin North Am 18:727-43
Rosenblum, L A; Coplan, J D; Friedman, S et al. (1994) Adverse early experiences affect noradrenergic and serotonergic functioning in adult primates. Biol Psychiatry 35:221-7

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