ADMA, SDMA AND L-ARGININE MAY BE NOVEL TARGETS IN PHARMACOTHERAPY FOR COMPLICATIONS DUE TO CARDIOPULMONARY BYPASS

dc.contributor.authorKahraman, Aydin
dc.contributor.authorMutlu, Emre
dc.contributor.authorAldag, Mustafa
dc.date.accessioned2026-08-12T17:04:44Z
dc.date.issued2017
dc.departmentFırat Üniversitesi
dc.description.abstractBackground: In this study, the effects of olmesartan therapy on asymmetric dimethylarginine (ADMA), symmetric di-methylarginine (SDMA), L-arginine and inducible nitric oxide synthase (iNOS) levels were investigated in patients undergoing cardiopulmonary bypass. Methods: Patients were randomly allocated to two groups, control and olmesartan. Olmesartan was administered 30 mg once a day beginning from preoperative day 5 to post-operative day 28 and on operation day. Blood was drawn from all patients and ADMA, SDMA, L-arginine and iNOS levels were analyzed at six time points (T1: before anesthesia induction, T2: during cardiopulmonary bypass, T3: five min after the cross-clamp was removed, T4: after protamine infusion, T5: on postoperative day 3 and T6: on post-operative day 28). Results: In the olmesartan treated group, iNOS levels exhibited significant decreases at T2, T3, T4, T5 and T6 time points compared with control group (p < 0.001, p < 0.05, p < 0.001, p < 0.01, p < 0.05 respectively). ADMA levels were significantly lower in olmesartan treated group than in control group at T3, T4, T5 and T6 time points (p < 0.05, p < 0.05, p < 0.05, p < 0.01 respectively). SDMA levels at T2, T3 and T6 time points were higher in control group than olmesartan group. L-Arginine levels were significantly higher at T2 and T3 time points in olmesartan treated group than control group (p < 0.001, p < 0.01). Conclusions: It was concluded that administration of olmesartan reduced plasma ADMA, SDMA, iNOS levels and enhanced L-arginine level in CPB time and it could reduce potential postoperative complications through reducing oxidative stress and inflammatory response in the postoperative period after coronary bypass surgery.
dc.description.sponsorshipFirat University Scientific Research Projects Coordination Unit (FUBAP)
dc.description.sponsorshipWe would like to thank Firat University Scientific Research Projects Coordination Unit (FUBAP) for their financial support.
dc.identifier.doi10.1515/jomb-2016-0025
dc.identifier.endpage17
dc.identifier.issn1452-8258
dc.identifier.issn1452-8266
dc.identifier.issue1
dc.identifier.orcid0000-0003-1363-4267
dc.identifier.pmid28680344
dc.identifier.scopus2-s2.0-85011268642
dc.identifier.scopusqualityQ3
dc.identifier.startpage8
dc.identifier.urihttps://doi.org/10.1515/jomb-2016-0025
dc.identifier.urihttps://hdl.handle.net/11508/48842
dc.identifier.volume36
dc.identifier.wosWOS:000393585400002
dc.identifier.wosqualityQ4
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherDe Gruyter Open Ltd
dc.relation.ispartofJournal of Medical Biochemistry
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WoS_20260511
dc.subjectasymmetric dimethylarginine (ADMA)
dc.subjectsymmetric dimethylarginine (SDMA)
dc.subjectL-arginine
dc.subjectcardiopulmonary bypass (CPB)
dc.subjectrenin-angiotensin system
dc.titleADMA, SDMA AND L-ARGININE MAY BE NOVEL TARGETS IN PHARMACOTHERAPY FOR COMPLICATIONS DUE TO CARDIOPULMONARY BYPASS
dc.typeArticle

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