Intrathecal penetration of N-formimidoyl thienamycin in normal rabbits: potentiation by coadministration of renal dipeptidase enzyme inhibitor

Antimicrob Agents Chemother. 1983 Apr;23(4):634-6. doi: 10.1128/AAC.23.4.634.

Abstract

The intrathecal penetration of N-formimidoyl thienamycin (MK0787) with or without coadministration of the renal dipeptidase enzyme inhibitor (MK791) in normal rabbits was studied immediately before and after the third dose of 40 mg/kg infused intravenously at daily 6-h intervals. Mean +/- standard error peak concentrations in cerebrospinal fluid were 0.23 +/- 0.02 and 0.53 +/- 0.12 micrograms/ml without and with coadministration of MK791, respectively (P less than 0.05, Student's t test). Penetration into cerebrospinal fluid (based on the ratio of cerebrospinal fluid to plasma area under the concentration-time curves) were 4.4 and 6.0%, respectively. N-Formimidoyl thienamycin penetrated uninflamed meninges, and peak concentrations were significantly augmented by coadministration of MK791.

MeSH terms

  • Animals
  • Anti-Bacterial Agents / cerebrospinal fluid*
  • Cilastatin
  • Cyclopropanes / administration & dosage
  • Cyclopropanes / pharmacology*
  • Dipeptidases / antagonists & inhibitors*
  • Drug Synergism
  • Female
  • Imipenem
  • Kidney / enzymology
  • Meningitis / drug therapy
  • Rabbits
  • Thienamycins / administration & dosage
  • Thienamycins / cerebrospinal fluid*

Substances

  • Anti-Bacterial Agents
  • Cyclopropanes
  • Thienamycins
  • Cilastatin
  • Imipenem
  • Dipeptidases