Εμφάνιση απλής εγγραφής

dc.creatorVeskoukis A.S., Paschalis V., Kyparos A., Nikolaidis M.G.en
dc.date.accessioned2023-01-31T10:32:43Z
dc.date.available2023-01-31T10:32:43Z
dc.date.issued2018
dc.identifier10.1016/j.redox.2018.01.001
dc.identifier.issn22132317
dc.identifier.urihttp://hdl.handle.net/11615/80602
dc.description.abstractMaximal velocity (Vmax) is a well established biomarker for the assessment of tissue redox status. There is scarce evidence, though, that it does not probably reflect sufficiently in vivo tissue redox profile. Instead, the Michaelis constant (Km) could more adequately image tissue oxidative stress and, thus, be a more physiologically relevant redox biomarker. Therefore, the aim of the present study was to side-by-side compare Vmax and Km of an antioxidant enzyme after implementing an in vivo set up that induces alterations in tissue redox status. Forty rats were divided into two groups including rats injected with blood plasma originating from rats that had previously swam until exhaustion and rats injected with blood plasma originating from sedentary rats. Tail-vein injections were performed daily for 21 days. Catalase Vmax and Km measured in gastrocnemius muscle were increased after administration of the exercise-conditioned plasma, denoting enhancement of the enzyme activity but impairment of its affinity for the substrate, respectively. These alterations are potential adaptations stimulated by the administered plasma pointing out that blood is an active fluid capable of regulating tissue homeostasis. Our findings suggest that Km adequately reflects in vivo modifications of skeletal muscle catalase and seems to surpass Vmax regarding its physiological relevance and biological interpretation. In conclusion, Km can be regarded as an in vivo-like biomarker that satisfactorily images the intracellular environment, as compared to Vmax that could be aptly parallelized with a biomarker that describes tissue oxidative stress in an in vitro manner. © 2018en
dc.language.isoenen
dc.sourceRedox Biologyen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85040070339&doi=10.1016%2fj.redox.2018.01.001&partnerID=40&md5=765da513cdfce44bc70015667ab3749e
dc.subjectcatalaseen
dc.subjectantioxidanten
dc.subjectbiological markeren
dc.subjectcatalaseen
dc.subjectadulten
dc.subjectanimal experimenten
dc.subjectanimal tissueen
dc.subjectArticleen
dc.subjectbinding affinityen
dc.subjectcontrolled studyen
dc.subjectenzyme activityen
dc.subjectenzyme kineticsen
dc.subjectenzyme substrate complexen
dc.subjectexerciseen
dc.subjectgastrocnemius muscleen
dc.subjectin vitro studyen
dc.subjectin vivo studyen
dc.subjectmaleen
dc.subjectnonhumanen
dc.subjectoxidation reduction stateen
dc.subjectplasmaen
dc.subjectpriority journalen
dc.subjectraten
dc.subjectadaptationen
dc.subjectanimalen
dc.subjectanimal experimenten
dc.subjectkineticsen
dc.subjectmetabolismen
dc.subjectoxidation reduction reactionen
dc.subjectoxidative stressen
dc.subjectskeletal muscleen
dc.subjectWistar raten
dc.subjectAdaptation, Physiologicalen
dc.subjectAnimalsen
dc.subjectAntioxidantsen
dc.subjectBiomarkersen
dc.subjectCatalaseen
dc.subjectKineticsen
dc.subjectMuscle, Skeletalen
dc.subjectOxidation-Reductionen
dc.subjectOxidative Stressen
dc.subjectPhysical Conditioning, Animalen
dc.subjectRatsen
dc.subjectRats, Wistaren
dc.subjectElsevier B.V.en
dc.titleAdministration of exercise-conditioned plasma alters muscle catalase kinetics in rat: An argument for in vivo-like Km instead of in vitro-like Vmaxen
dc.typejournalArticleen


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