Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/4721
Title: Nitric oxide, adenosine deaminase, xanthine oxidase and superoxide dismutase in patients with panic disorder: Alterations by antidepressant treatment
Authors: Herken, Hasan
Akyol, O.
Yilmaz, H.R.
Tutkun, H.
Savas, H.A.
Ozen, M.E.
Kalenderoglu, A.
Keywords: Adenosine deaminase
Nitric oxide
Panic disorder
Superoxide dismutase
Treatment response
Xanthine oxidase
adenosine deaminase
alprazolam
antidepressant agent
citalopram
fluoxetine
fluvoxamine
nitric oxide
serotonin uptake inhibitor
superoxide dismutase
xanthine oxidase
adolescent
adult
article
blood sampling
controlled study
correlation analysis
diagnostic and statistical manual of mental disorders
disease association
enzyme activity
enzyme blood level
female
human
major clinical study
male
panic
pathophysiology
priority journal
prognosis
protein blood level
protein function
questionnaire
rating scale
semi structured interview
spectrophotometry
statistical significance
treatment outcome
treatment response
Turkey (republic)
Adenosine
Adolescent
Adult
Antidepressive Agents
Case-Control Studies
Female
Humans
Male
Middle Aged
Nitric Oxide
Panic Disorder
Spectrum Analysis
Superoxide Dismutase
Xanthine Oxidase
Abstract: Objective: In the present study, we aimed to investigate whether nitric oxide (NO) levels and activities of xanthine oxidase (XO), superoxide dismutase (SOD), and adenosine deaminase (ADA) are associated with Panic disorder (PD) as well as impact of psychopharmacological treatments on NO, SOD, ADA, and XO levels in PD. Method: In this study, 32 patients and 20 healthy controls were included. The serum levels of NO, XO, SOD, and ADA were measured in the patients and controls. The patients were treated with antidepressant. Results: ADA and XO levels of the patients were significantly higher than the controls. SOD levels of the patients were significantly lower than the controls but the difference was not statistically significant. Although NO levels of the patients were higher than the controls, the difference was not statistically significant. There was no correlation between PAS and the parameters studied (SOD, ADA, XO, and NO) of the patients. After 8 weeks of antidepressant treatment, ADA and SOD activities were increased whereas NO and XO levels decreased significantly. Conclusion: ADA, XO activity may have a pathophysiological role in PD, and prognosis of PD. Activity of these enzymes may be used to monitor effects of the antidepressant treatment. Copyright © 2005 John Wiley & Sons, Ltd.
URI: https://hdl.handle.net/11499/4721
https://doi.org/10.1002/hup.742
ISSN: 0885-6222
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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