Literature DB >> 2552905

Influence of daptomycin on staphylococcal abscesses and experimental tobramycin nephrotoxicity.

C A Wood1, H C Finkbeiner, S J Kohlhepp, P W Kohnen, D N Gilbert.   

Abstract

The antibacterial efficacies of daptomycin and vancomycin were compared in male Fischer rats with subcutaneous abscesses caused by either methicillin-susceptible Staphylococcus aureus (MSSA) or methicillin-resistant S. aureus (MRSA). The influence of daptomycin on tobramycin nephrotoxicity was also assessed. MSSA or MRSA abscesses were treated with subcutaneous daptomycin (10 mg/kg every 12 h), vancomycin (125 mg/kg every 12 h), or diluent (every 12 h) for 5 to 10 days. Rats in both antibiotic treatment groups had lower abscess bacterial counts than did controls at days 5 and 10 (P less than 0.0025). The daptomycin treatment groups had lower abscess bacterial counts than did the vancomycin treatment groups for MSSA at day 5 (P less than 0.0025) and day 10 (P less than 0.025) and for MRSA at day 10 (P less than 0.0025). Nephrotoxicity treatment groups included animals treated for 3, 7, 10, 14, and 17 days with subcutaneous diluent (every 12 h), daptomycin (20 mg/kg every 12 h), tobramycin (40 mg/kg every 12 h), and the combination of daptomycin and tobramycin. Compared with controls, animals treated with daptomycin alone exhibited no detectable nephrotoxicity. Rats given tobramycin alone developed functional and histopathologic abnormalities from days 7 through 17. Animals treated with daptomycin and tobramycin for 14 days had a lower mean concentration of creatinine in serum (P less than 0.005), higher mean creatinine clearance values (P less than 0.05), and less cortical tubular cell regeneration (P less than 0.05) than did rats treated with tobramycin alone. In rats with staphylococcal subcutaneous abscesses, daptomycin was superior to vancomycin in treating both MSSA and MRSA. Daptomycin alone caused no detectable renal injury, and in rats given daptomycin combined with tombramycin, there was less histologic and functional renal injury than in animals given tobramycin alone.

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Year:  1989        PMID: 2552905      PMCID: PMC172640          DOI: 10.1128/AAC.33.8.1280

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.191


  20 in total

1.  Inhibition of peptidoglycan biosynthesis in gram-positive bacteria by LY146032.

Authors:  N E Allen; J N Hobbs; W E Alborn
Journal:  Antimicrob Agents Chemother       Date:  1987-07       Impact factor: 5.191

2.  Antimicrobial activity and spectrum of LY146032, a lipopeptide antibiotic, including susceptibility testing recommendations.

Authors:  R N Jones; A L Barry
Journal:  Antimicrob Agents Chemother       Date:  1987-04       Impact factor: 5.191

3.  In vitro activity of a new cyclic lipopeptide antibiotic, LY146032, against gram-positive clinical bacteria.

Authors:  P Huovinen; P Kotilainen
Journal:  Antimicrob Agents Chemother       Date:  1987-03       Impact factor: 5.191

4.  In-vitro susceptibility of gram-positive cocci to LY146032 teicoplanin, sodium fusidate, vancomycin, and rifampicin.

Authors:  D J Pohlod; L D Saravolatz; M M Somerville
Journal:  J Antimicrob Chemother       Date:  1987-08       Impact factor: 5.790

5.  Comparative in-vitro activity of LY146032 a new peptolide, with vancomycin and eight other agents against gram-positive organisms.

Authors:  C A Benson; F Beaudette; G Trenholm
Journal:  J Antimicrob Chemother       Date:  1987-08       Impact factor: 5.790

6.  In-vitro activity of LY146032 against Staphylococcus aureus and S. epidermidis.

Authors:  P E Coudron; J L Johnston; G L Archer
Journal:  J Antimicrob Chemother       Date:  1987-10       Impact factor: 5.790

7.  Activity of LY146032 compared with that of methicillin, cefazolin, cefamandole, cefuroxime, ciprofloxacin, and vancomycin against staphylococci as determined by kill-kinetic studies.

Authors:  C W Stratton; C Liu; L S Weeks
Journal:  Antimicrob Agents Chemother       Date:  1987-08       Impact factor: 5.191

8.  Comparison of the investigational drug, LY146032, with vancomycin in experimental pneumonia due to methicillin-resistant Staphylococcus aureus.

Authors:  P A Kephart; A L Esposito
Journal:  J Antimicrob Chemother       Date:  1988-01       Impact factor: 5.790

9.  Comparison of cefazolin, cefamandole, vancomycin, and LY146032 for prophylaxis of experimental Staphylococcus epidermidis endocarditis.

Authors:  L J Wheat; J W Smith; J Reynolds; A T Bemis; T Treger; J A Norton
Journal:  Antimicrob Agents Chemother       Date:  1988-01       Impact factor: 5.191

10.  Polyaspartic acid prevents experimental aminoglycoside nephrotoxicity.

Authors:  D N Gilbert; C A Wood; S J Kohlhepp; P W Kohnen; D C Houghton; H C Finkbeiner; J Lindsley; W M Bennett
Journal:  J Infect Dis       Date:  1989-05       Impact factor: 5.226

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  10 in total

1.  Attenuation of gentamicin-induced nephrotoxicity in rats by fleroxacin.

Authors:  D Beauchamp; G Laurent; L Grenier; P Gourde; J Zanen; J A Heuson-Stiennon; M G Bergeron
Journal:  Antimicrob Agents Chemother       Date:  1997-06       Impact factor: 5.191

2.  In vitro activities of daptomycin, arbekacin, vancomycin, and gentamicin alone and/or in combination against glycopeptide intermediate-resistant Staphylococcus aureus in an infection model.

Authors:  R L Akins; M J Rybak
Journal:  Antimicrob Agents Chemother       Date:  2000-07       Impact factor: 5.191

3.  Effects of daptomycin and vancomycin on tobramycin nephrotoxicity in rats.

Authors:  D Beauchamp; M Pellerin; P Gourde; M Pettigrew; M G Bergeron
Journal:  Antimicrob Agents Chemother       Date:  1990-01       Impact factor: 5.191

4.  Ceftriaxone protects against tobramycin nephrotoxicity.

Authors:  D Beauchamp; G Thériault; L Grenier; P Gourde; S Perron; Y Bergeron; L Fontaine; M G Bergeron
Journal:  Antimicrob Agents Chemother       Date:  1994-04       Impact factor: 5.191

5.  Daptomycin may attenuate experimental tobramycin nephrotoxicity by electrostatic complexation to tobramycin.

Authors:  M Couture; M Simard; P Gourde; C Lessard; K Gurnani; L Lin; D Carrier; M G Bergeron; D Beauchamp
Journal:  Antimicrob Agents Chemother       Date:  1994-04       Impact factor: 5.191

6.  Subcellular distribution of daptomycin given alone or with tobramycin in renal proximal tubular cells.

Authors:  D Beauchamp; P Gourde; M Simard; M G Bergeron
Journal:  Antimicrob Agents Chemother       Date:  1994-02       Impact factor: 5.191

7.  Temporal variation in nephrotoxicity of low doses of isepamicin in rats.

Authors:  Y Yoshiyama; L Grenier; P Gourde; M Simard; L Lin; N J Morin; M G Bergeron; G Labrecque; D Beauchamp
Journal:  Antimicrob Agents Chemother       Date:  1996-03       Impact factor: 5.191

8.  Attenuation by daptomycin of gentamicin-induced experimental nephrotoxicity.

Authors:  N Thibault; L Grenier; M Simard; M G Bergeron; D Beauchamp
Journal:  Antimicrob Agents Chemother       Date:  1994-05       Impact factor: 5.191

9.  Beta-lactams versus glycopeptides in treatment of subcutaneous abscesses infected with Staphylococcus aureus.

Authors:  C A Wood; R M Wisniewski
Journal:  Antimicrob Agents Chemother       Date:  1994-05       Impact factor: 5.191

Review 10.  Daptomycin: a cyclic lipopeptide antimicrobial agent.

Authors:  LilyAnn Jeu; Horatio B Fung
Journal:  Clin Ther       Date:  2004-11       Impact factor: 3.393

  10 in total

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