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dc.contributor.authorAYKAC-TOKER, G
dc.contributor.authorKocak-Toker, N
dc.contributor.authorBULGURCUOGLU, S
dc.date.accessioned2021-03-05T12:57:12Z
dc.date.available2021-03-05T12:57:12Z
dc.date.issued2001
dc.identifier.citationAYKAC-TOKER G., BULGURCUOGLU S., Kocak-Toker N., "Effect of peroxynitrite on glutaredoxin", HUMAN & EXPERIMENTAL TOXICOLOGY, cilt.20, ss.373-376, 2001
dc.identifier.issn0960-3271
dc.identifier.otherav_afc30ce3-39da-4e86-b6e1-4d7dbbc8ebb4
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/117198
dc.identifier.urihttps://doi.org/10.1191/096032701680350578
dc.description.abstractGlutaredoxin is an important enzyme in thiol homeostasis. As a thioltransferase, it reduces oxidized thiols. It also has dehydroascorbate reductase (DHAR) activity to reduce dehydroascorbate (DHA) to ascorbic acid. Peroxynitrite (ONOO-) is one of the most active elements of oxidative stress that can be formed wherever nitric oxide and superoxide are produced simultaneously. ONOO- is known to react with free thiols easily. To observe the effect of ONOO- on glutaredoxin, rat liver cytosolic fractions were incubated with 0-250 muM ONOO-. Thioltransferase activity was found to be decreased as ONOO- concentration increased. The inhibition was not reversible with dithiothreitol (DTT). In cytosol besides glutaredoxin, another enzyme with DHAR activity is also present. In our study, the cytosolic DHAR activity which consisted both enzymes, was also inhibited by ONOO-, but DTT was able to return the activity almost completely.
dc.language.isoeng
dc.subjectTemel Bilimler
dc.subjectEczacılık
dc.subjectYaşam Bilimleri
dc.subjectMeslek Bilimleri
dc.subjectFarmasötik Toksikoloji
dc.subjectSağlık Bilimleri
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectFarmakoloji ve Toksikoloji
dc.subjectTOKSİKOLOJİ
dc.titleEffect of peroxynitrite on glutaredoxin
dc.typeMakale
dc.relation.journalHUMAN & EXPERIMENTAL TOXICOLOGY
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume20
dc.identifier.issue7
dc.identifier.startpage373
dc.identifier.endpage376
dc.contributor.firstauthorID17031


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