Interaction of zinc in pancreatic β-cells with reduced form of gluthation as possible cause of its protective activity

dc.contributor.authorMeyramov, G.G.
dc.contributor.authorKorchin, V.I.
dc.contributor.authorShaybek, A.S.
dc.contributor.authorGagolina, S.V.
dc.contributor.authorAndreewa, A.P.
dc.contributor.authorZhuzbaeva, G.O.
dc.date.accessioned2018-05-05T07:57:03Z
dc.date.available2018-05-05T07:57:03Z
dc.date.issued2018-03-30
dc.description.abstractIt is known that Zinc which is contains in pancreatic β-cells of take participation in formation of deposited storage form of insulin in cells. It is known now a 18 Diabetogenic zinc binding β-cytotoxic chemicals (DZC) which in β-cells formed toxic chelat complexes that result destruction and death of β-cells within 15–30 min. and developing of diabetes. Among 18 DZC 17 of them are belong to derivatives of 8-oxyquinolin which are a components of more than 10 pharmaceutical drugs. It is known also that administration of amino acid a Reduced form of Glutathione completely protect pancreatic B-cells of destruction and prevent developing of diabetes caused by DZC. It is supposed that this property of Glutathione is determined by its ability to block of zinc in B-cells and to prevent interaction of it with DZC. Authors using of sensitive and high specific histochemical methods established that only Reduced form of Glutathione contains of SH-radical in structure of molecule blocked zinc ions in β-cells and protect of its from destruction caused by DZC contrary to Oxidized form of Glutathione not contains of SH-radical, not blocking of zinc ions in β-cells and not protect formation of zinc-DZC complexes in β-cells accompanied by death of cells. Authors suppose that in process of formation of toxic complexes as zinc-DZC atom of zinc is fixed between atom of S from SH-radicals of two molecules of Reduced form of Glutathione or between atom of O of a carboxyl group and atom of S of SHradical of molecule of Glutathione as in result of interaction of zinc with diabetognic derivatives of 8-oxyquinolin.ru_RU
dc.identifier.citationВзаимодействие цинка в панкреатических β-клетках с восстановленной формой глютатиона как возможная причина его защитного действия/G.G. Meyramov [et al]//Қарағанды универисетінің хабаршысы. БИОЛОГИЯ. МЕДИЦИНА. ГЕОГРАФИЯ Сериясы.=Вестник Карагандинского университета. Серия БИОЛОГИЯ. МЕДИЦИНА. ГЕОГРАФИЯ.=Bulletin of the Karaganda University. BIOLOGY. MEDICINE. GEOGRAPHY Series.-2018. №3.Р.50-57.ru_RU
dc.identifier.urihttps://rep.buketov.edu.kz/handle/data/2829
dc.language.isoenru_RU
dc.publisherKSU Publ.ru_RU
dc.relation.ispartofseriesҚарағанды универисетінің хабаршысы. БИОЛОГИЯ. МЕДИЦИНА. ГЕОГРАФИЯ Сериясы.=Вестник Карагандинского университета. Серия БИОЛОГИЯ. МЕДИЦИНА. ГЕОГРАФИЯ.=Bulletin of the Karaganda University. BIOLOGY. MEDICINE. GEOGRAPHY Series.;№ 1(89)/2018
dc.subjectpancreasru_RU
dc.subjectpancreatic isletsru_RU
dc.subjectβ-cellsru_RU
dc.subjecthistochemical methodsru_RU
dc.subjectdithizonru_RU
dc.subject8-para(toluenesulphonylamino) quinolinru_RU
dc.subjectzincru_RU
dc.subjectinsulinru_RU
dc.subjectquantitative analysisru_RU
dc.titleInteraction of zinc in pancreatic β-cells with reduced form of gluthation as possible cause of its protective activityru_RU
dc.title.alternativeПанкреатикалық β-жасушаларындағы қалпына келтірілген глютатион түрімен оның қорғаныш əрекетінің ықтимал себебі ретінде мырыштың өзара əрекеттесуіru_RU
dc.title.alternativeВзаимодействие цинка в панкреатических β-клетках с восстановленной формой глютатиона как возможная причина его защитного действияru_RU
dc.typeArticleru_RU

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