HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Effect of experimental renal failure on the pharmacodynamics of cefoselis-induced seizures in rats.

Abstract
We investigated the effect of infusion rate and experimental renal failure on the pharmacodynamics of cefoselis (CFSL)-induced seizures. As an animal model of CFSL-induced seizures, male Wistar rats received an intravenous infusion of CFSL at one of three different rates (1.4-5.8 g/h/rat) until the onset of maximal seizures (which occurred after 8.0 to 36.0 min of infusion). Samples of cerebrospinal fluid (CSF), blood (for serum), and brain were obtained immediately after stopping infusion of CSFL. The serum concentration of CFSL at the onset of seizures increased with increasing infusion rate, but brain and CSF concentrations of CFSL at the onset of seizures were not affected by the infusion rate. Ureter-ligated (UL) and control rats received an intravenous infusion of CFSL at 1.4 g/h/rat until the onset of seizures. Then the same procedure as used to determine the effect of infusion rate on the concentrations of CFSL was carried out. Renal failure was associated with a significant decrease in the amount of CFSL required to induce seizures. Serum, brain, and CSF concentrations of CFSL in UL rats were significantly lower than those in control rats. These results indicate that the experimental strategy and animal model in this investigation would be useful to assess the effects of diseases and other variables on the pharmacodynamics of CFSL-induced seizures and that renal failure is one of the risk factors for neurotoxicity of CFSL.
AuthorsM Nagata, M Yasuhara
JournalBiological & pharmaceutical bulletin (Biol Pharm Bull) Vol. 24 Issue 9 Pg. 1049-52 (Sep 2001) ISSN: 0918-6158 [Print] Japan
PMID11558567 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Cephalosporins
  • Convulsants
  • cefoselis
  • Ceftizoxime
Topics
  • Acute Kidney Injury (complications, metabolism)
  • Animals
  • Ceftizoxime (analogs & derivatives, pharmacokinetics, toxicity)
  • Cephalosporins (pharmacokinetics, toxicity)
  • Convulsants (pharmacokinetics, toxicity)
  • Male
  • Rats
  • Rats, Wistar
  • Seizures (chemically induced, complications, metabolism)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: