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dc.contributor.authorLAYCOCK, SK
dc.contributor.authorMCMURRAY, J
dc.contributor.authorKANE, KA
dc.contributor.authorPARRATT, JR
dc.date.accessioned2022-02-18T09:15:46Z
dc.date.available2022-02-18T09:15:46Z
dc.date.issued1993
dc.identifier.citationLAYCOCK S., MCMURRAY J., KANE K., PARRATT J., "EFFECTS OF THE XANTHINE-OXIDASE SYSTEM ON CARDIAC-FUNCTION IN ANESTHETIZED RATS", FREE RADICAL BIOLOGY AND MEDICINE, cilt.15, sa.3, ss.249-255, 1993
dc.identifier.issn0891-5849
dc.identifier.othervv_1032021
dc.identifier.otherav_299878b8-6bb7-4468-b4eb-c0f03716269a
dc.identifier.urihttp://hdl.handle.net/20.500.12627/176851
dc.identifier.urihttps://doi.org/10.1016/0891-5849(93)90071-2
dc.description.abstractThis investigation aimed to determine whether contractile dysfunction of the myocardium could be produced upon generation of free radicals in the anaesthetised rat. The enzyme xanthine oxidase, combined with its substrate purine and an iron source, was used to generate free radicals in the venous circulation. The suspended form of xanthine oxidase, with substrate, produced a transient, significant depression in the contractile indices dP dt-1 max and dP dt-1 P-1 and arterial blood pressure, 1146 +/- 87 mm Hg s-1, 9 +/- 1 s-1, and 18 +/- 1 mm Hg, respectively. This could not be attenuated by the enzymatic free radical scavengers superoxide dismutase and catalase. Furthermore, the suspended xanthine oxidase alone or its vehicle were able to produce a similar effect to that of the complete free-radical-generating system. The maximum soluble dose of the crystalline form of the enzyme when employed in the generating system had no effect upon administration despite its production of superoxide radicals in vitro. These results suggest that the haemodynamic effects of the free-radical-generating system containing the suspended form of xanthine oxidase were due to the effects of its vehicle and that the free-radical-generating system containing the crystalline form of the enzyme did not produce sufficient free radicals in vivo to modify myocardial contractility.
dc.language.isoeng
dc.subjectBİYOKİMYA VE MOLEKÜLER BİYOLOJİ
dc.subjectDrug Discovery
dc.subjectAging
dc.subjectGeneral Biochemistry, Genetics and Molecular Biology
dc.subjectBiochemistry
dc.subjectStructural Biology
dc.subjectEndocrinology, Diabetes and Metabolism
dc.subjectLife Sciences
dc.subjectHealth Sciences
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectENDOKRİNOLOJİ VE METABOLİZMA
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectİç Hastalıkları
dc.subjectEndokrinoloji ve Metabolizma Hastalıkları
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectSitogenetik
dc.subjectTemel Bilimler
dc.subjectBiochemistry, Genetics and Molecular Biology (miscellaneous)
dc.subjectEndocrinology
dc.subjectClinical Biochemistry
dc.subjectCancer Research
dc.subjectMolecular Biology
dc.subjectEndocrine and Autonomic Systems
dc.titleEFFECTS OF THE XANTHINE-OXIDASE SYSTEM ON CARDIAC-FUNCTION IN ANESTHETIZED RATS
dc.typeMakale
dc.relation.journalFREE RADICAL BIOLOGY AND MEDICINE
dc.contributor.department, ,
dc.identifier.volume15
dc.identifier.issue3
dc.identifier.startpage249
dc.identifier.endpage255
dc.contributor.firstauthorID3370984


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