A Comparison between the Nephrotoxic Profile of Gentamicin and Gentamicin Nanoparticles in Mice. Issue 2 (8th October 2014)

• Record Type: Journal Article
• Authors: Jamshidzadeh, Akram; Heidari, Reza; Mohammadi‐Samani, Soliman; Azarpira, Negar; Najbi, Asma; Jahani, Parisa; Abdoli, Narges
• Is Part Of: Journal of biochemical and molecular toxicology. Volume 29:Issue 2(2015:Feb.)
• Page Start: 57
• Page End: 62
• Publication Date: 2014-10-08
• Subjects: Biochemistry -- Periodicals; Molecular biology -- Periodicals; Toxicology -- Periodicals; 574
• DOI: 10.1002/jbt.21667
• Languages: English
• ISSNs: 1095-6670

Abstract

<abstract abstract-type="main"> <title>ABSTRACT</title> <p>Aminoglycoside antibiotics are widely used against Gram‐negative infections. On the other hand, nephrotoxicity is a deleterious side effect associated with aminoglycoside therapy. Gentamicin is the most nephrotoxic aminoglycoside. Because of serious health complications ensue the nephrotoxicity induced by aminoglycosides, finding new therapeutic strategies against this problem has a great clinical value. This study has attempted to compare the nephrotoxic properties of gentamicin and a new nanosized formulation of this drug in a mice model. Animals were treated with gentamicin (100 mg/kg, i.p. for eight consecutive days) and nanogentamicin (100 mg/kg, i.p. for eight consecutive days). Blood urea nitrogen (BUN), plasma creatinine levels, and histopathological changes of kidney proximal tubule were monitored. It was found that gentamicin caused severe degeneration of kidney proximal tubule cells and an increase in serum creatinine and BUN. No severe injury was observed after nanogentamicin administration. This study proved that nanosized gentamicin is less nephrotoxic.</p> </abstract>