作者: V.Craig Jordan , V.Daniel Castracane
DOI: 10.1016/0090-6980(76)90140-4
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摘要: Abstract Aspirin, indomethacin and naproxen have been shown to inhibit the release of prostaglandins E F (PGE PGF) from estradiol-stimulated uterus progesterone-pretreated ovariectomized rats. Under present experimental conditions (1 mg/rat) was found be a potent inhibitor PGF biosynthesis, but duration action less than 24 hours, after which rebound above control levels observed. The compounds were without effect on increases in uterine wet weight. Δ′THC did not PG biosynthesis produced significant rise (P