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dc.contributor.authorTamer-Toptani, S
dc.contributor.authorTurkoglu, UM
dc.contributor.authorUysal, M
dc.contributor.authorToker, GA
dc.contributor.authorOztezcan, S
dc.date.accessioned2021-03-04T09:59:26Z
dc.date.available2021-03-04T09:59:26Z
dc.date.issued1998
dc.identifier.citationTurkoglu U., Oztezcan S., Tamer-Toptani S., Uysal M., Toker G., "The effect of N-acetyl-cysteine and N-omega-nitro-L-arginine methyl ester treatment on lipopolysaccharide-induced oxidative stress in lung of rats", BIOCHEMICAL ARCHIVES, cilt.14, sa.2, ss.139-146, 1998
dc.identifier.issn0749-5331
dc.identifier.othervv_1032021
dc.identifier.otherav_6afa6b05-364a-4745-93bf-8ff7f6b3b0fa
dc.identifier.urihttp://hdl.handle.net/20.500.12627/73998
dc.description.abstractIn the present study we investigated the effects of N-omega-Nitro-L-arginine methyl ester (L-NAME), an inhibitor of nitric oxide synthase (NOS) and N-acetyl-cysteine (NAC) on the activities of myeloperoxidase (MPO), xanthine oxidase (XO) and lipid peroxide levels as well as glutathione (GSH) levels and superoxide dismutase (SOD) activities in the lung of lipopolysaccharide (LPS)-treated rats. LPS treatment (5 mg/kg) caused a decrease in the GSH level and SOD activity while it led to increases in lipid peroxide levels and MPO and XO activities in the lung. LPS + L-NAME + NAC administration prevented GSH reduction and MPO, XO and lipid peroxide augmentation. The factors causing oxidative stress after LPS-treatment was found to be ameliorated following L-NAME + NAC treatment. The data suggest that L-NAME and NAC treatment together may have some beneficial effect on LPS induced lung injury.
dc.language.isoeng
dc.subjectSitogenetik
dc.subjectTemel Bilimler
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectYaşam Bilimleri
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectBİYOKİMYA VE MOLEKÜLER BİYOLOJİ
dc.titleThe effect of N-acetyl-cysteine and N-omega-nitro-L-arginine methyl ester treatment on lipopolysaccharide-induced oxidative stress in lung of rats
dc.typeMakale
dc.relation.journalBIOCHEMICAL ARCHIVES
dc.contributor.department, ,
dc.identifier.volume14
dc.identifier.issue2
dc.identifier.startpage139
dc.identifier.endpage146
dc.contributor.firstauthorID120686


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