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dc.creatorMamoulakis C., Fragkiadoulaki I., Karkala P., Georgiadis G., Zisis I.-E., Stivaktakis P., Kalogeraki A., Tsiaoussis I., Burykina T., Lazopoulos G., Tsarouhas K., Kouretas D., Tsatsakis A.en
dc.date.accessioned2023-01-31T08:56:36Z
dc.date.available2023-01-31T08:56:36Z
dc.date.issued2019
dc.identifier10.1016/j.toxrep.2019.04.007
dc.identifier.issn22147500
dc.identifier.urihttp://hdl.handle.net/11615/76242
dc.description.abstractIdentification of novel biomarkers of contrast-induced nephropathy (CIN)that may more accurately detect renal function changes; reflect kidney damage; assist monitoring; and elucidate pathophysiology attract considerable scientific attention nowadays. To evaluate novel biomarkers of nephrotoxicity in blood/tissue samples of a CIN model, 10 New Zealand white rabbits were divided into group 1 (n = 5; iopromide)and group 2 (n = 5; control). Blood was drawn at 0 h (immediately), 24 h and 48 h after contrast medium (CM)administration. Animals were euthanized at 48 h and kidneys were removed. Serum creatinine (sCr)/symmetric-asymmetric dimethylarginine (SDMA-ADMA)levels were measured. CM genotoxic/cytotoxic effect was investigated 48 h post-CM exposure using micronucleus assay in lymphocytes. Cytological examination was conducted using touch preparation technique (TPT). All animals in group 1 developed CIN: mean sCr levels increased by 68.2% within 48 h. Significant SDMA-ADMA level elevation was observed at 0 h and 24 h with insignificant drop at 48 h in group 1, remaining normal in group 2 at all time-points. Significant increase in bi-nucleated cells with micronuclei and micronuclei frequency was detected in group 1. Cytokinesis block proliferation index was reduced insignificantly in group 1. TPT revealed degenerative lesions/inflammation, cell degeneration, abnormal uterine tubular casts and rubella in kidneys of all animals in group 1. Group 2 presented normal cells. © 2019 The Authorsen
dc.language.isoenen
dc.sourceToxicology Reportsen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85065150045&doi=10.1016%2fj.toxrep.2019.04.007&partnerID=40&md5=32a4bae994f13c33d0254f00a9838712
dc.subjectbiological markeren
dc.subjectcontrast mediumen
dc.subjectcreatinineen
dc.subjectdimethylargininaseen
dc.subjectiopromideen
dc.subjectacute kidney failureen
dc.subjectanimal experimenten
dc.subjectanimal modelen
dc.subjectanimal tissueen
dc.subjectapoptosisen
dc.subjectArticleen
dc.subjectcell degenerationen
dc.subjectcell proliferationen
dc.subjectcontrast induced nephropathyen
dc.subjectcontrolled studyen
dc.subjectcytokinesisen
dc.subjectcytotoxicityen
dc.subjectgenotoxicityen
dc.subjectinflammationen
dc.subjectLeporidaeen
dc.subjectliquid chromatography-mass spectrometryen
dc.subjectmaleen
dc.subjectmicronucleusen
dc.subjectnephrotoxicityen
dc.subjectnonhumanen
dc.subjectpriority journalen
dc.subjectrubellaen
dc.subjectElsevier Inc.en
dc.titleContrast-induced nephropathy in an animal model: Evaluation of novel biomarkers in blood and tissue samplesen
dc.typejournalArticleen


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