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dc.contributor.authorAvcıkurt, Ayla Solmaz
dc.contributor.authorKöçkar, Feray
dc.contributor.authorSinan, Selma
dc.date.accessioned2019-10-17T07:35:59Z
dc.date.available2019-10-17T07:35:59Z
dc.date.issued2015en_US
dc.identifier.issn1742-464X
dc.identifier.issn1742-4658
dc.identifier.urihttps://hdl.handle.net/20.500.12462/7652
dc.description.abstractThe human paraoxonase (hPON) gene family includes threemembers: PON1, PON2, and PON3, located adjacent to eachother on the long arm of chromosome 7. The three hPONs shareapproximately 65% identity at the amino acid level and 70%identity at the nucleotide level. In humans, hPON1 and hPON3are primarily expressed in liver while expression of hPON3 is alsofound in kidney. In contrast, hPON2 is more widely expressedand is found in a variety of tissues including the heart, kidney,liver, lung, placenta, small intestine, spleen, stomach, and testis.The effect of PON2 enzyme that is strictly expressed in macro-phages. The aim of the study is to determine thein vitroeffect ofCefazolin sodium, Gentamycin sulphate, ampicillin sodium andChloramphenicol sodium succinate on PON2 enzyme in humanmacrophages cell, namely U937 cells. Two different substrateswere used for the determination enzyme activity of PON2, lactoseand phenylacetate Different concentrations of drug were used inorder to see any effect on PON2 enzyme. These antibiotics revealthe differential effects on PON2 enzyme in U937 macrophages atdifferent time points and concentrations of drugs.en_US
dc.language.isoengen_US
dc.publisherWiley-Blackwellen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectParaoxonaseen_US
dc.subjectParaoxonase 2en_US
dc.subjectAntibioticsen_US
dc.subjectInhibitionen_US
dc.subjectActivationen_US
dc.subjectU937 Cellsen_US
dc.titleThe determination of effect of some antibiotics on paraoxonase 2 (PON2) enzyme activities in human macrophages cellen_US
dc.typeotheren_US
dc.relation.journalFebs Journalen_US
dc.contributor.departmentFen Edebiyat Fakültesien_US
dc.identifier.volume282en_US
dc.identifier.issue1en_US
dc.identifier.startpage84en_US
dc.identifier.endpage84en_US
dc.relation.publicationcategoryDiğeren_US


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