| dc.creator | 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. | en |
| dc.date.accessioned | 2023-01-31T08:56:36Z | |
| dc.date.available | 2023-01-31T08:56:36Z | |
| dc.date.issued | 2019 | |
| dc.identifier | 10.1016/j.toxrep.2019.04.007 | |
| dc.identifier.issn | 22147500 | |
| dc.identifier.uri | http://hdl.handle.net/11615/76242 | |
| dc.description.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 | en |
| dc.language.iso | en | en |
| dc.source | Toxicology Reports | en |
| dc.source.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85065150045&doi=10.1016%2fj.toxrep.2019.04.007&partnerID=40&md5=32a4bae994f13c33d0254f00a9838712 | |
| dc.subject | biological marker | en |
| dc.subject | contrast medium | en |
| dc.subject | creatinine | en |
| dc.subject | dimethylargininase | en |
| dc.subject | iopromide | en |
| dc.subject | acute kidney failure | en |
| dc.subject | animal experiment | en |
| dc.subject | animal model | en |
| dc.subject | animal tissue | en |
| dc.subject | apoptosis | en |
| dc.subject | Article | en |
| dc.subject | cell degeneration | en |
| dc.subject | cell proliferation | en |
| dc.subject | contrast induced nephropathy | en |
| dc.subject | controlled study | en |
| dc.subject | cytokinesis | en |
| dc.subject | cytotoxicity | en |
| dc.subject | genotoxicity | en |
| dc.subject | inflammation | en |
| dc.subject | Leporidae | en |
| dc.subject | liquid chromatography-mass spectrometry | en |
| dc.subject | male | en |
| dc.subject | micronucleus | en |
| dc.subject | nephrotoxicity | en |
| dc.subject | nonhuman | en |
| dc.subject | priority journal | en |
| dc.subject | rubella | en |
| dc.subject | Elsevier Inc. | en |
| dc.title | Contrast-induced nephropathy in an animal model: Evaluation of novel biomarkers in blood and tissue samples | en |
| dc.type | journalArticle | en |