Role of sodium in the protective effect of ticarcillin on gentamicin nephrotoxicity in rats

Author:

Ohnishi A1,Bryant T D1,Branch K R1,Sabra R1,Branch R A1

Affiliation:

1. Division of Clinical Pharmacology, Vanderbilt University, Nashville, Tennessee 37232.

Abstract

Coadministration of sodium ticarcillin with an aminoglycoside is known to reduce the nephrotoxicity of the aminoglycoside. However, it is not known whether the penicillin or the obligatory sodium load confers protection. To investigate this, gentamicin has been administered intraperitoneally in doses of 50, 60, or 80 mg/kg per day for 12 days in groups of rats receiving either a normal or a low sodium intake. Alterations in creatinine clearance have been measured. Salt depletion resulted in an enhanced nephrotoxic response with a shift in the dose-response curve to the left. Administration of sodium ticarcillin to rats with a salt-depleted intake at a dose sufficient to replace sodium intake conferred an equal degree of protection to rats with a normal salt intake. We report that the obligatory salt supplement with ticarcillin is sufficient to account for the renal sparing effect of the combination treatment without having to infer a direct chemical interaction of penicillin with the aminoglycoside.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

Reference36 articles.

1. Nephrotoxicity of antimicrobial agents;Appel G. B.;N. Engl. J. Med.,1977

2. Aminoglycoside accumulation kinetics in rat renal parenchyma;Aronoff G. R.;Antimicrob. Agents Chemother.,1983

3. Effect of sodium intake on gentamicin nephrotoxicity in the rat;Bennett W. M.;Proc. Soc. Exp. Biol. Med.,1976

4. Inactivation of amikacin and gentamicin by carbenicillin in patients with end-stage renal failure;Blair D. C.;Antimicrob. Agents Chemother.,1982

5. Protection from gentamicin nephrotoxicity by aphalothin and carbenicillin;Block R.;Antimicrob. Agents Chemother.,1979

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