Source of F series prostaglandins during the early postpartum period in cattle
In vivo and in vitro studies were conducted to determine the contribution of the bovine uterus to concentrations of 15-keto-13,14-dihydro-prostaglandin F2 alpha (PGFM) in peripheral plasma of postpartum cows. In Experiment 1, cows were assigned to three groups: untreated control (n = 4), hysterectom...
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Veröffentlicht in: | Biology of reproduction 1984-12, Vol.31 (5), p.879-887 |
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Zusammenfassung: | In vivo and in vitro studies were conducted to determine the contribution of the bovine uterus to concentrations of 15-keto-13,14-dihydro-prostaglandin
F2 alpha (PGFM) in peripheral plasma of postpartum cows. In Experiment 1, cows were assigned to three groups: untreated control
(n = 4), hysterectomy following a manually induced prolapse of the uterus (n = 5) and sham operation (n = 3: prolapse of the
uterus and replacement). Surgery was performed within 8 h of parturition, and blood samples collected frequently on the day
of surgery and once (0800 h) or twice (0800 and 1700 h) daily from Day 1 to Day 15 postpartum. Following hysterectomy, PGFM
concentrations decreased precipitously, became essentially undetectable by 5 h, and remained so for the rest of the experimental
period. In contrast (P less than 0.01), PGFM concentrations, which remained elevated during the day of surgery in the sham-operated
group, peaked on Day 2 (sham-operated group: 1339 pg/ml) or Day 3 (untreated control: 2143 pg/ml), and declined to a basal
concentration between Days 10 to 15. In Experiment 2, in vitro metabolism of tritiated arachidonic acid ([3H] AA: 10 microCi)
and production of PGF2 alpha and PGFM were studied in explants of early postpartum intrauterine tissues (myometrium, caruncle
and intercaruncular endometrium). Extracts of [3H] AA metabolites released into the incubation medium were separated on Sephadex
LH-20 column chromatography. Metabolites of [3H] AA, having the same chromatographic mobility as PGF2 alpha, PGFM and PGE2,
were detected. |
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ISSN: | 0006-3363 1529-7268 |
DOI: | 10.1095/biolreprod31.5.879 |