Comparative pharmacokinetics of cefoperazone and cephradine in untreated streptozotocin diabetic rats

E. Nakashima, R. Matsushita, M. Takeda, T. Nakanishi, F. Ichimura

Research output: Contribution to journalArticle

13 Citations (Scopus)

Abstract

Experimental diabetes mellitus was induced in adult male rats by injecting streptozotocin (STZ; 60 mg/kg iv) for the purpose of surveying changes in the pharmacokinetics of biliary excretion after the intravenous administration of 40 mg/kg of cefoperazone (CPZ) or cephradine (CED). CPZ, CED, and other organic anions share affinity for the organic anion transport system in the bile canalicular membrane. The STZ treatment had a marked influence on the distribution and elimination of both cephalosporins. The blood levels of both cephalosporins at each time point after administration differed significantly between the STZ-treated and control rats. The values of mean residence time (MRT) of CPZ and CED were significantly decreased in the STZ-treated rats. Basal bile flow rates were increased after the administration of CPZ in the control and STZ-treated rats. Biliary clearance (CL(bile)) of CPZ was more than 60% of the CL(tot), whereas CL(bile) of CED was less than 20% of CL(tot) in both groups of rats. The mean CL(bile) value of CPZ in the STZ-treated rats was 1.0 ml/min higher than that of the control rats, whereas the mean CL(bile) value of CED was almost the same as that of the control rats. The increased CL(bile) of CPZ suggested that diabetes alters the biliary excretion of CPZ. The changes in MRT of CPZ in the STZ-treated and control rats are mainly caused by an increase in the biliary excretory rate and renal clearance. The changes in MRT of CED in the STZ-treated and control rats are caused by a decrease in the apparent volume of distribution and increased renal clearance.

Original languageEnglish
Pages (from-to)730-735
Number of pages6
JournalDrug Metabolism and Disposition
Volume20
Issue number5
Publication statusPublished - 1992
Externally publishedYes

Fingerprint

Cephradine
Cefoperazone
Pharmacokinetics
Streptozocin
Rats
Rat control
Bile
Cephalosporins
Medical problems
Anions
Kidney
Surveying
Experimental Diabetes Mellitus
Intravenous Administration
Blood
Flow rate

ASJC Scopus subject areas

  • Pharmacology
  • Toxicology

Cite this

Nakashima, E., Matsushita, R., Takeda, M., Nakanishi, T., & Ichimura, F. (1992). Comparative pharmacokinetics of cefoperazone and cephradine in untreated streptozotocin diabetic rats. Drug Metabolism and Disposition, 20(5), 730-735.

Comparative pharmacokinetics of cefoperazone and cephradine in untreated streptozotocin diabetic rats. / Nakashima, E.; Matsushita, R.; Takeda, M.; Nakanishi, T.; Ichimura, F.

In: Drug Metabolism and Disposition, Vol. 20, No. 5, 1992, p. 730-735.

Research output: Contribution to journalArticle

Nakashima, E, Matsushita, R, Takeda, M, Nakanishi, T & Ichimura, F 1992, 'Comparative pharmacokinetics of cefoperazone and cephradine in untreated streptozotocin diabetic rats', Drug Metabolism and Disposition, vol. 20, no. 5, pp. 730-735.
Nakashima, E. ; Matsushita, R. ; Takeda, M. ; Nakanishi, T. ; Ichimura, F. / Comparative pharmacokinetics of cefoperazone and cephradine in untreated streptozotocin diabetic rats. In: Drug Metabolism and Disposition. 1992 ; Vol. 20, No. 5. pp. 730-735.
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