Murine Teratology of Fluconazole: Evaluation of Developmental Phase Specificity and Dose Dependence

The potential of in utero exposure to fluconazole to initiate teratogenesis was analyzed in ICR (CD-1) mice. Developmental phase specificity was determined by treating mice with single oral doses of 700 mg/kg on gestational day 8, 9, 10, 11, or 12. Control animals received vehicle on gestational days 8–12. Gestational day 10 was identified as the phase of maximal sensitivity for induction of cleft palate, the predominant teratogenic effect induced by fluconazole, with 50% of fetuses exposed on this developmental phase being affected. After treatments on gestational day 8, 9, 11, or 12, cleft palate occurred with lower frequencies: 12, 21, 28.7, and 2.7%, respectively. Examination of skeletal morphology revealed anomalies of the middle ear apparatus in 15% of the fetuses that were exposed on gestational day 8. Dysmorphic tympanic ring and absence of the incus were the more common ear anomalies recorded. Reduced humeral length was noted in 22% of fetuses that were exposed on gestational day 10. Dose-response relationship was investigated by treating animals with 0 (vehicle), 87.5, 175, or 350 mg/kg on gestational day 10, coincident with the phase of peak teratogenic sensitivity. Besides showing that fluconazole operates under a strict dose-response mechanism, the study identified 175 mg/kg as the lowest observed adverse effect level for cleft palate induction, with 7.6% of the exposed fetuses being affected.

[1]  R. Brent Utilization of animal studies to determine the effects and human risks of environmental toxicants (drugs, chemicals, and physical agents). , 2004, Pediatrics.

[2]  W. Inman,et al.  Safety of fluconazole in the treatment of vaginal candidiasis , 2004, European Journal of Clinical Pharmacology.

[3]  V. Massa,et al.  Relationship between hindbrain segmentation, neural crest cell migration and branchial arch abnormalities in rat embryos exposed to fluconazole and retinoic acid in vitro. , 2004, Reproductive toxicology.

[4]  E. Menegola,et al.  Pathogenic pathways in fluconazole-induced branchial arch malformations. , 2003, Birth defects research. Part A, Clinical and molecular teratology.

[5]  J. Friedman,et al.  Medical genetics: 1. Clinical teratology in the age of genomics. , 2002, CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne.

[6]  W. Webster,et al.  Is this drug safe in pregnancy? , 2001, Reproductive toxicology.

[7]  E. Menegola,et al.  Antifungal triazoles induce malformations in vitro. , 2001, Reproductive toxicology.

[8]  M. Mallo,et al.  Formation of the middle ear: recent progress on the developmental and molecular mechanisms. , 2001, Developmental biology.

[9]  H. Sørensen,et al.  Risk of malformations and other outcomes in children exposed to fluconazole in utero. , 1999, British journal of clinical pharmacology.

[10]  S. Jick Pregnancy Outcomes after Maternal Exposure to Fluconazole , 1999, Pharmacotherapy.

[11]  P. Kaufmann The anatomical basis of mouse development , 1999 .

[12]  D. Bartley,et al.  Multiple malformation syndrome following fluconazole use in pregnancy: report of an additional patient. , 1997, American journal of medical genetics.

[13]  D. Debruyne Clinical Pharmacokinetics of Fluconazole in Superficial and Systemic Mycoses , 1997, Clinical pharmacokinetics.

[14]  P. Mastroiacovo,et al.  Prospective assessment of pregnancy outcomes after first-trimester exposure to fluconazole. , 1996, American journal of obstetrics and gynecology.

[15]  J. Abraham,et al.  Fluconazole-induced congenital anomalies in three infants. , 1996, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

[16]  T. Gridley,et al.  Development of the mammalian ear: coordinate regulation of formation of the tympanic ring and the external acoustic meatus. , 1996, Development.

[17]  G. Tiboni Second branchial arch anomalies induced by fluconazole, a bis-triazole antifungal agent, in cultured mouse embryos. , 1993, Research communications in chemical pathology and pharmacology.

[18]  A. R. Murthy,et al.  Congenital malformations in an infant born to a woman treated with fluconazole. , 1992, The Pediatric infectious disease journal.

[19]  L. Fernando,et al.  Transfusion-acquired hepatitis A outbreak from fresh frozen plasma in a neonatal intensive care unit. , 1992, The Pediatric infectious disease journal.

[20]  M J Humphrey,et al.  Pharmacokinetic evaluation of UK-49,858, a metabolically stable triazole antifungal drug, in animals and humans , 1985, Antimicrobial Agents and Chemotherapy.

[21]  W. Scott,et al.  Potentiation of acetazolamide induced ectrodactyly in SWV and C57BL/6J mice by cadmium sulfate. , 1984, Teratology.

[22]  C A Kimmel,et al.  A rapid procedure for routine double staining of cartilage and bone in fetal and adult animals. , 1981, Stain technology.

[23]  井上 稔 Differential Staining of Cartilage and Bone in Fetal Mouse Skeleton by Alcian Blue and Alizarin Red S , 1976 .

[24]  J. Wilson Methods for administering agents and detecting malformations in experimental animals , 1965 .