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Contrast-induced nephropathy in an animal model: Evaluation of novel biomarkers in blood and tissue samples

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Autore
Mamoulakis 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.
Data
2019
Language
en
DOI
10.1016/j.toxrep.2019.04.007
Soggetto
biological marker
contrast medium
creatinine
dimethylargininase
iopromide
acute kidney failure
animal experiment
animal model
animal tissue
apoptosis
Article
cell degeneration
cell proliferation
contrast induced nephropathy
controlled study
cytokinesis
cytotoxicity
genotoxicity
inflammation
Leporidae
liquid chromatography-mass spectrometry
male
micronucleus
nephrotoxicity
nonhuman
priority journal
rubella
Elsevier Inc.
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Abstract
Identification 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 Authors
URI
http://hdl.handle.net/11615/76242
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