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Teratogenic effects of mescaline, epinephrine, and norepinephrine in the hamster

Kenneth S. Hirsch, Hans Fritz

Teratology June 1, 1981 DOI: 10.1002/tera.1420230302 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Experimental study Peer reviewed
Population Pregnant cream-strain hamsters
Interventions Mescaline Epinephrine Norepinephrine
Dose 16 and 32 mg/kg (mescaline); 500 μg/kg (epinephrine and norepinephrine)
Duration Gestation days 7–10
Topics Mescaline
Keywords Hamster Norepinephrine Pharmacology
Citations 19
Key findings Mescaline caused dose-dependent increases in embryo resorptions and delayed skeletal ossification in hamsters, and both epinephrine and norepinephrine also impaired reproductive success and ossification.

Abstract

Abstract Mescaline was administered orally at doses of 16 and 32 mg/kg on the seventh through tenth days of gestation to pregnant cream‐strain hamsters. This treatment resulted in a dose‐dependent effect on reproductive success and skeletal ossification. The effect of mescaline on reproductive success included an increased number of resorptions resulting in a decreased litter size. The 32 mg/kg dose of mescaline caused 48.8% resorptions, while 16 mg/kg and control animals had 12.0% and 6.4% resorptions, respectively. Litter size was decreased from 12.0 pups in controls to 10.3 (16 mg/kg) and 6.5 (32 mg/kg) pups per litter in treated groups. No gross abnormalities were observed at necropsy; there was, however, a dose‐dependent increased delay in the ossification of the skull, sternum, and metatarsals. Both epinephrine and norepinephrine caused a decrease in reproductive success when administered at 500 μg/kg. Epinephrine appeared to cause a trend towards preimplantation wastage as indicated by an increased corpora lutea to implantation site ratio (from 1.3–1.9). Norepinephrine, however, caused an increased number of resorptions (29.1% in controls). Both norepinephrine and epinephrine produced similar delays in ossification.

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