5-HT1A receptor binding in panic disorder; comparison with depressive disorder and healthy volunteers using PET and [11C]WAY-100635

NeuroImage ◽  
2000 ◽  
Vol 11 (5) ◽  
pp. S189 ◽  
Author(s):  
P. Sargent ◽  
J. Nash ◽  
S. Hood ◽  
E. Rabiner ◽  
C. Messa ◽  
...  
2008 ◽  
Vol 193 (3) ◽  
pp. 229-234 ◽  
Author(s):  
Jon R. Nash ◽  
Peter A. Sargent ◽  
Eugenii A. Rabiner ◽  
Sean D. Hood ◽  
Spilios V. Argyropoulos ◽  
...  

BackgroundThe importance of the neurotransmitter serotonin (5-HT) in the pathophysiology of anxiety is well known. A key role for postsynaptic 5-HT1A receptors has recently been suggested in studies of genetic knockout mice.AimsTo measure 5-HT1A receptor binding in patients with panic disorder in the untreated state and after recovery on treatment with selective serotonin reuptake inhibitors (SSRIs).MethodNine symptomatic untreated patients with panic disorder, seven patients recovered on SSRI medication and nineteen healthy volunteers underwent a single positron emission tomography (PET) scan using the 5-HT1A tracer [11C]WAY-100635.ResultsIn comparison with controls, both presynaptic and postsynaptic 5-HT1A receptor binding was reduced in untreated patients, with the most significant reductions being in the raphe, orbitofrontal cortex, temporal cortex and amygdala. In recovered patients presynaptic binding was reduced, but there was no significant reduction in postsynaptic binding.ConclusionsPanic disorder is associated with reduced 5-HT1A receptor availability, which is also known to have a key role in depression.


2020 ◽  
Author(s):  
Samuel David Clark

AbstractThe kappa opioid receptor (KOR) and its endogenous ligands dynorphins (DYN) have been implicated in the development or symptomatology of a variety of neuropsychiatric disorders. This review covers a brief history of the development of KOR agonists and antagonists, their effects in healthy volunteers, and the potential role of DYN/KOR dysfunction in schizophrenia and major depressive disorder from a translational perspective. The potential role of DYN/KOR dysfunction in schizophrenia is based on several lines of evidence. Selective KOR agonists induce affective states in healthy volunteers with similarities to the symptoms of schizophrenia. Studies have shown increased DYN in patients with schizophrenia, although the data have been mixed. Finally, meta-analytic data have shown that opioid antagonists are associated with reductions in the symptoms of schizophrenia. The potential role of DYN/KOR dysfunction in major depressive disorder is also based on a combination of preclinical and clinical data. Selective KOR agonists have shown pro-depressive effects in human volunteers, while selective KOR antagonists have shown robust efficacy in several preclinical models of antidepressant activity. Small studies have shown that nonselective KOR antagonists may have efficacy in treatment-resistant depression. Additionally, recent clinical data have shown that the KOR may be an effective target for treating anhedonia, a finding relevant to both schizophrenia and depression. Finally, recommendations are provided for translating preclinical models for schizophrenia and major depressive disorder into the clinic.


2016 ◽  
Vol 26 (3) ◽  
pp. 570-577 ◽  
Author(s):  
Jani Penttilä ◽  
Jussi Hirvonen ◽  
Lauri Tuominen ◽  
Ville Lumme ◽  
Tuula Ilonen ◽  
...  

1984 ◽  
Vol 13 (2) ◽  
pp. 93-96 ◽  
Author(s):  
Donald R. Sweeney ◽  
Mark S. Gold ◽  
A. L. C. Pottash ◽  
David Martin

Five patients with panic disorder were placed on low doses of imipramine. All patients had shown dramatic improvement after three weeks of treatment, when plasma levels of imipramine and desipramine were measured. Plasma levels corresponded to the low doses being administered. This result implies that the mechanism of action of tricyclic antidepressants is different in patients with panic disorder than in patients with depressive disorder.


1995 ◽  
Vol 37 (4) ◽  
pp. 224-228 ◽  
Author(s):  
Murray B. Stein ◽  
Suzanne M. Delaney ◽  
Mariette J. Chartier ◽  
Cara D.L. Kroft ◽  
Andrea L. Hazen

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