Evaluation of valproic acid (VPA) developmental toxicity and pharmacokinetics in Sprague-Dawley rats

P. E. Binkerd, J. M. Rowland, H. Nau, Andrew G Hendrickx

Research output: Contribution to journalArticle

Abstract

This study was undertaken to assess the pharmacokinetics and developmental toxicity of the anticonvulsant, valproic acid (VPA), a human teratogen, in Sprague-Dawley rats. Oral administration of 200-800 mg/kg VPA (5-20 × human therapeutic dose) from Gestational Days (GD) 8 to 17 resulted in increasing maternal toxicity at the higher doses with 100% maternal lethality at 800 mg/kg. Although there was an increased incidence of resorptions at 600 mg/kg (48 ± 43%) compared to controls (18 ± 24%), it was not statistically significant. Fetal examination on GD 20 revealed dose-dependent fetal growth retardation (p ≤0.05) as evidenced by decreased fetal weight and length in addition to underossification of both the axial and appendicular skeleton. The incidence of skeletal defects, including abnormal vertebrae, ribs, and craniofacial dysmorphia, also increased with higher doses of VPA. Cardiac anomalies observed in the two highest treatment groups consisted of great vessel malformations with or without associated ventricular septal defects (VSDs). Urogenital defects were also noted in the 600 mg/kg group. The plasma elimination half-life on GD 8 was 1.0 ± 0.3 hr at 200 mg/kg and 2.3 ± 0.7 hr at 600 mg/kg. Maximal concentrations of total and free drug were 341 ± 18 μg/ml and 181 ± 11 μg/ml, respectively, in the low-dose group and 911 ± 379 μg/ml and 542 ± 224 μg/ml in the high-dose group. No significant changes in any pharmacokinetic parameters (t 1 2, AUC, Cmax, tmax) were observed over the 10-day treatment period at either dose level.

Original languageEnglish (US)
Pages (from-to)485-493
Number of pages9
JournalFundamental and Applied Toxicology
Volume11
Issue number3
DOIs
StatePublished - 1988

ASJC Scopus subject areas

  • Toxicology

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