Effects of daptomycin and vancomycin on tobramycin nephrotoxicity in rats
Open Access
- 1 January 1990
- journal article
- research article
- Published by American Society for Microbiology in Antimicrobial Agents and Chemotherapy
- Vol. 34 (1) , 139-147
- https://doi.org/10.1128/aac.34.1.139
Abstract
Daptomycin is a new biosynthetic antibiotic which belongs to a new class of drugs known as lipopeptides. The objective of this study was to evaluate the effects of daptomycin and vancomycin on tobramycin-induced nephrotoxicity. Female Sprague-Dawley rats were treated during 4 and 10 days with either saline (NaCl, 0.9%) or tobramycin at doses of 4 and 40 mg/kg per day (given every 12 h [q12h] intraperitoneally). Each treatment was combined with saline, daptomycin at a dose of 20 mg/kg per day (given q12h subcutaneously), and ancomycin at a dose of 50 mg/kg per day (given q12h subcutaneously). Daptomycin and vancomycin had no effect on the intracortical accumulation of tobramycin. Daptomycin did not accumulate in renal tissue even after 10 days of treatment. Tobramycin given at a dose of 40 mg/kg per day during 10 days induced a significant inhibition of sphingomyelinase activity in the renal cortex (P less than 0.01) and increased cellular regeneration (P less than 0.01), as measured by the incorporation of [3H]thymidine into DNA of the renal cortex. These changes were minimal when daptomycin was combined with tobramycin. Histologically, signs of tobramycin toxicity were also less severe in the presence of daptomycin. The intracortical accumulation of vancomycin was not modified by tobramycin. The sphingomyelinase activity was significantly more inhibited (P less than 0.01) when vancomycin was associated with tobramycin (4 and 40 mg/kg) without affecting the rate of [3H]thymidine incorporation into DNA. Histologically, signs of tobramycin toxicity were not affected by vancomuycin, but the cellular vacuolizations which were also observed in vancomycin-treated animals were still present in the proximal tubular cells of animals that were treated with the combination vancomycin-tobramycin. This study strongly suggests that daptomycin protects animals from tobramycin-induced nephrotoxicity but that vancomycin may enhance the effect of tobramycin. We conclude that daptomycin is safe and protects kidney cells from tobramycin-induced nephrotoxicity.This publication has 36 references indexed in Scilit:
- Polyaspartic Acid Prevents Experimental Aminoglycoside NephrotoxicityThe Journal of Infectious Diseases, 1989
- In-vitro susceptibility of Gram-positive cocci to LY146032 teicoplanin, sodium fusidate, vancomycin, and rifampicinJournal of Antimicrobial Chemotherapy, 1987
- Comparative in-vitro activity of LY146032 a new peptolide, with vancomycin and eight other agents against Gram-positive organismsJournal of Antimicrobial Chemotherapy, 1987
- Lack of Nephrotoxicity in Pediatric Patients Receiving Concurrent Vancomycin and Aminoglycoside TherapyChemotherapy, 1987
- Impairment of lysosome-pinocytic vesicle fusion in rat kidney proximal tubules after treatment with gentamicin at low dosesToxicology and Applied Pharmacology, 1986
- A prospective study of adverse reactions associated with vancomycin therapyJournal of Antimicrobial Chemotherapy, 1985
- Renal tolerance and pharmacokinetics of vancomycin in ratsJournal of Antimicrobial Chemotherapy, 1984
- Gentamicin-induced nephrotoxicity: A cell biology approachKidney International, 1980
- Autoradiography of gentamicin uptake by the rat proximal tubule cellKidney International, 1979
- The renal handling of polybasic drugsNaunyn-Schmiedebergs Archiv für experimentelle Pathologie und Pharmakologie, 1977