Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/4347
Title: Adenosine Deaminase, Nitric Oxide, Superoxide Dismutase, and Xanthine Oxidase in Patients with Major Depression: Impact of Antidepressant Treatment
Authors: Herken, Hasan
Gurel, A.
Selek, S.
Armutcu, F.
Ozen, M.E.
Bulut, M.
Kap, O.
Keywords: Adenosine deaminase
Antidepressant
Depression
Nitric oxide
Superoxide dismutase
Xanthine oxidase
adenosine deaminase
antidepressant agent
citalopram
fluoxetine
fluvoxamine
nitric oxide
oxygen radical
serotonin uptake inhibitor
sertraline
superoxide dismutase
xanthine oxidase
adolescent
adult
article
clinical article
controlled study
diagnostic and statistical manual of mental disorders
enzyme activity
enzyme blood level
female
Hamilton scale
human
major depression
male
monitoring
pathophysiology
prognosis
treatment outcome
Adenosine Deaminase
Adolescent
Adult
Antidepressive Agents
Depressive Disorder, Major
Female
Humans
Male
Middle Aged
Nitric Oxide
Prognosis
Superoxide Dismutase
Xanthine Oxidase
Abstract: Background: There has been much evidence in recent years that free oxygen radicals and nitric oxide (NO) may play an important role in the pathophysiology of neuropsychiatric disorders. In this study, we aimed to investigate whether NO, xanthine oxidase (XO), superoxide dismutase (SOD), and adenosine deaminase (ADA) levels are associated with major depression (MD) and to evaluate the impact of antidepressant treatments on NO, SOD, ADA and XO levels in MD. Methods: Thirty-six patients who were diagnosed as MD according to DSM-IV criteria and 20 healthy controls were included. The serum levels of NO, XO, SOD, and ADA were measured by spectrophotometric methods both in patients and controls. Patients were treated with antidepressant drugs for 8 weeks. All patients were assessed by Hamilton Depression Rating Scale (HDRS) both before and after antidepressant treatment. Results: ADA and XO levels of the patients were significantly higher than the controls. SOD level of the patients was significantly lower than the controls. Although NO levels of the patients were higher than the controls, the difference was not statistically significant. There was no correlation between HDRS 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. Conclusions: ADA, XO, and SOD activity may have a pathophysiological role in MD and may predict prognosis of MD. Activity of these enzymes may be used to monitor effects of the antidepressant treatment. © 2007 IMSS.
URI: https://hdl.handle.net/11499/4347
https://doi.org/10.1016/j.arcmed.2006.10.005
ISSN: 0188-4409
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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