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Vol. 298, Issue 2, 797-804, August 2001
Department of Pharmacology and Toxicology, Medical College of
Virginia Campus, Virginia Commonwealth University, Richmond, Virginia
The developmental effects of exposure to various doses of
buprenorphine, methadone, or water during the perinatal period were studied in the rat. Rats were exposed to buprenorphine (0.3, 1.0, or
3.0 mg/kg/day), methadone (9 mg/kg/day), and/or water prenatally, postnatally, or both pre- and postnatally, via maternally implanted osmotic minipumps. Fetal and maternal mortality and morbidity were
assessed, as well as the acquisition of several developmental milestones, pup weight gain, precipitated withdrawal, and the antinociceptive effect of morphine. Although perinatal exposure to
buprenorphine failed to produce severe maternal and fetal or neonatal
mortality, it was associated with a significant amount of perinatal
mortality and perturbations of pup development. Pups developed physical
dependence to both drugs, as evidenced by the ability of naloxone
challenge to precipitate withdrawal. Both drugs induced tolerance to
the antinociceptive effects of morphine in the tail-flick test. The
effects of buprenorphine varied with the dose used, and the highest
dose did not always produce the greatest effect. There were some
similarities between the effects of perinatal buprenorphine and
perinatal methadone; however, differences were also observed between
the effects of the two drugs, which may be related to the different
affinities and efficacies of the drugs at different opioid receptor subtypes.