| Literature DB >> 26996880 |
Yaremi Quirós1, Victor Blanco-Gozalo1, Jose I Sanchez-Gallego1, Francisco J López-Hernandez2, Juan Ruiz3, María P Perez de Obanos3, José M López-Novoa4.
Abstract
Aminoglycosides are very effective antibiotics for the treatment of severe infections, but they rank among the most frequent causes of drug-induced nephrotoxicity. Thus, prevention of aminoglycoside nephrotoxicity is an unmet therapeutic objective. Cardiotrophin-1 (CT-1), a member of the IL-6 family of cytokines, has been reported to protect the kidney against toxic and ischemic acute kidney injury (AKI). We have assessed the effect of rat CT-1 in the severity of gentamicin (G)-induced AKI. Groups of male Wistar rats received the following for 6 consecutive days: i) isotonic saline solution (group CONT), ii) G, 150mg/kg/day, i.p. (group G), iii) CT-1, 100μg/kg/day i.v. (group CT-1), or iv) G and CT-1 at the doses described above. The G group showed a manifest AKI characterized by low creatinine clearance, high plasma creatinine and urea levels, increased urinary excretion of proteins, glucose and AKI markers such as N-acetyl-glucosaminidase, neutrophil gelatinase-associated lipocalin, kidney-injury molecule-1 and T-gelsolin, increased kidney levels of CD-68, iNOS, IL-1β and TNF-α, and markedly higher histological renal damage and leukocyte infiltration than the CONT and CT-1 groups. Administration of CT-1 together with G reduced almost all of the above-described manifestations of G-induced AKI. The results of this study have potential clinical application, as CT-1 is near to being used as a drug for organ protection.Entities:
Keywords: Acute kidney injury; Aminoglycoside; Cardiotrophin-1; Gentamicin; Nephroprotection
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Year: 2016 PMID: 26996880 DOI: 10.1016/j.phrs.2016.02.025
Source DB: PubMed Journal: Pharmacol Res ISSN: 1043-6618 Impact factor: 7.658