Abstract
The effects of maternal treatment with ritodrine, a β2-adrenergic agonist, on the biochemical development of fetal brain were studied in an animal model. Pregnant rats were treated with long and short dosage schedules. Fetuses were delivered by hysterotomy 4 h after the last dose. No differences in the fetal brain content of protein, DNA, glycogen, cholesterol or β-adrenergic receptors were found. In this animal model, using relatively high maternal doses of ritodrine, there were no apparent effects on the fetal brain biochemical indices measured, suggesting a relatively high efficacy to toxicity ratio of ritodrine for brain development.
Original language | English |
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Pages (from-to) | 76-85 |
Number of pages | 10 |
Journal | Developmental Pharmacology and Therapeutics |
Volume | 5 |
Issue number | 1-2 |
DOIs | |
State | Published - 1 Jan 1982 |
Externally published | Yes |
ASJC Scopus subject areas
- General Pharmacology, Toxicology and Pharmaceutics
- Pharmacology (medical)