Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/21551
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dc.date.accessioned2021-08-27T08:56:48Z-
dc.date.available2021-08-27T08:56:48Z-
dc.date.issued2006-
dc.identifier.citationSarandol, A. vd. (2006). ''Oxidation of apolipoprotein B-containing lipoproteins and serum paraoxonase/arylesterase activities in major depressive disorder''. Progress in Neuro-Psychopharmacology and Biological Psychiatry, 30(6), 1103-1108.en_US
dc.identifier.issn0278-5846-
dc.identifier.issn1878-4216-
dc.identifier.urihttps://doi.org/10.1016/j.pnpbp.2006.04.012-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0278584606001692-
dc.identifier.urihttp://hdl.handle.net/11452/21551-
dc.description.abstractMajor depressive disorder (MDD) is blaimed to play a role in the onset of coronary artery disease (CAD). The aim of the present study was to investigate serum paraoxonase/arylesterase activities and oxidation of apolipoprotein B-containing lipoproteins in patients with MDD. Oxidation of lipoproteins plays an important role in atherogenesis and the enzyme paraoxonase, has been shown to prevent lipoprotein oxidation. Furthermore, low paraoxonase activity was suggested to predict CAD. Eighty-six patients who fully met the fourth Diagnostic and Statistical Manual of Mental Disorders criteria for MDD and 36 healthy control subjects were included in the study. Serum paraoxonase and arylesterase activities were determined spectrophotometrically. Malondialdehyde (MDA) levels of apolipoprotein B-containing lipoproteins were determined before (basal) and after incubation with copper-sulphate, that yielded basal- and Delta-MDA values, respectively. Serum paraoxonase/arylesterase activities were significantly reduced in the post-treatment group compared with the pre-treatment group. Basal-MDA (MDA) level was significantly higher in the MDD group compared with the control group. Delta-MDA level of the severe MDD group was significantly higher than that of the control group. There was a positive correlation between the oxidizability of apolipoprotein B-containing lipoproteins and the severity of the disease. Total cholesterol, HDL-cholesterol, LDL-cholesterol, apolipoprotein B levels were significantly higher and apolipoprotein AI levels were significantly lower in the MDD group compared with those of the control group. The findings of the present study suggest that: 1) antidepressant treatment might reduce serum paraoxonase activity/mass; 2) oxidation and oxidizability of apolipoprotein B-containing lipoproteins seem to be increased in MDD.en_US
dc.language.isoenen_US
dc.publisherPergamon-Elsevier Scienceen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectNeurosciences & neurologyen_US
dc.subjectPharmacology & pharmacyen_US
dc.subjectPsychiatryen_US
dc.subjectParaoxonaseen_US
dc.subjectMajor depressive disorderen_US
dc.subjectLipoprotein oxidationen_US
dc.subjectLipiden_US
dc.subjectCoronary artery diseaseen_US
dc.subjectAylesteraseen_US
dc.subjectPolymorphismen_US
dc.subjectSymptomsen_US
dc.subjectCholesterolen_US
dc.subjectCardiac risken_US
dc.subjectCardiovascular-diseaseen_US
dc.subjectMyocardial-infarctionen_US
dc.subjectRaoxonase arylesteraseen_US
dc.subjectRisk-factorpaen_US
dc.subjectCoronary-artery-diseaseen_US
dc.subjectLow-densityen_US
dc.subjectLipoproteinen_US
dc.titleOxidation of apolipoprotein B-containing lipoproteins and serum paraoxonase/arylesterase activities in major depressive disorderen_US
dc.typeArticleen_US
dc.identifier.wos000239008600017tr_TR
dc.identifier.scopus2-s2.0-33745225923tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Psikiyatri Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Biyokimya Anabilim Dalı.tr_TR
dc.contributor.orcid0000-0002-2593-7196tr_TR
dc.identifier.startpage1103tr_TR
dc.identifier.endpage1108tr_TR
dc.identifier.volume30tr_TR
dc.identifier.issue1tr_TR
dc.relation.journalProgress in Neuro-Psychopharmacology and Biological Psychiatryen_US
dc.contributor.buuauthorSarandol, Aslı-
dc.contributor.buuauthorSarandol, Emre-
dc.contributor.buuauthorEker, Salih Saygın-
dc.contributor.buuauthorKaraağaç, Esra Uğurlu-
dc.contributor.buuauthorHızlı, Banu Zafer-
dc.contributor.buuauthorDirican, Melahat-
dc.contributor.buuauthorKirli, Selçuk-
dc.contributor.researcheridABE-1716-2020tr_TR
dc.contributor.researcheridQ-9477-2019tr_TR
dc.contributor.researcheridAAG-6985-2021tr_TR
dc.identifier.pubmed16716479tr_TR
dc.subject.wosClinical neurologyen_US
dc.subject.wosNeurosciencesen_US
dc.subject.wosPharmacology & pharmacyen_US
dc.subject.wosPsychiatryen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubmeden_US
dc.wos.quartileQ2en_US
dc.subject.scopusAryldialkylphosphatase; Arylesterase; Human PON1 Proteinen_US
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