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  • 1
    In: REPRODUCTION, Bioscientifica, Vol. 139, No. 3 ( 2010-03), p. 665-672
    Abstract: Cytokines are thought to regulate prostaglandin (PG) secretion in the bovine endometrium. However, there is no consensus about the role of interleukin-1α (IL1A) on PG secretion. The objective of this study was to examine the influence of IL1A on basal and interferon-τ (IFNT)-regulated PG in vitro secretion, as well its effects on PG secretion, progesterone (P 4 ) output, and corpus luteum (CL) in vivo lifespan. Explants of bovine endometrium (days 16–17 of the estrous cycle or early pregnancy) were stimulated with IL1A (10 ng/ml), IFNT (30 ng/ml), or IL1A combined with IFN. IL1A alone strongly stimulated luteotrophic PGE 2 secretion by endometrial tissues of both pregnant and nonpregnant cows. IL1A also stimulated luteolytic PGF 2α output in the late luteal phase. IFNT augmented the stimulatory effect of IL1A on PGE 2 secretion. In an in vivo experiment, saline or IL1A at different doses (0.001–10 μg/per animal) was applied to the uterine lumen on day 16 of the cycle. Only the highest dose of IL1A caused a temporal increase in PGF 2α secretion, while it had no effect on P 4 secretion or CL lifespan. Application of 0.1 and 1 μg IL1A stimulated P 4 and PGE 2 output and prolonged the CL lifespan. Although IL1A may stimulate in vitro luteolytic PGF 2α secretion during the estrous cycle, it only acts as a luteotrophic factor in vivo . IL1A increased luteotrophic PGE 2 and P 4 output, inhibiting spontaneous luteolysis. These luteotrophic effects may result in appropriate luteal development and function in cows during the estrous cycle and early pregnancy.
    Type of Medium: Online Resource
    ISSN: 1470-1626 , 1741-7899
    Language: Unknown
    Publisher: Bioscientifica
    Publication Date: 2010
    detail.hit.zdb_id: 2037813-0
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  • 2
    In: Journal of Endocrinology, Bioscientifica, Vol. 193, No. 1 ( 2007-04), p. 127-135
    Abstract: To determine whether glucocorticoids (GCs) play a role in regulating uterine function in cow, the present study examined the expression of mRNA encoding GC receptor (GC-R) α, 11β-hydroxysteroid dehydrogenase (11-HSD) type 1 and type 2, and the activity of 11-HSD1 in bovine endometrial tissue throughout the estrous cycle. We also studied the effects of cortisol on basal, oxytocin (OT)- and tumor necrosis factor-α (TNFα)-stimulated prostaglandin (PG) production. A quantitative real-time PCR analysis revealed that GC-Rα mRNA was expressed more strongly in the mid-luteal stage (days 8–12) than in the other stages. In contrast to GC-Rα mRNA expression, 11-HSD1 mRNA expression was greater in the follicular stage than in the other stages, whereas 11-HSD2 mRNA expression was lowest in the follicular stage. The activity of 11-HSD1 was greater in the follicular stage and estrus than in the other stages and was lowest in the mid-luteal stage. Cortisone was dose-dependently converted to cortisol in the cultured endometrial tissue. Although cortisol did not affect either the basal or OT-stimulated production of PGs in the cultured epithelial cells, the production of PGs stimulated by TNFα in the stromal cells was suppressed by cortisol ( P 〈 0.05). Cortisol suppressed basal prostaglandin (PG)F2α without affecting basal PGE2 production in the stromal cells. The overall results suggest that the level of cortisol is locally regulated in bovine endometrium throughout the estrous cycle by 11-HSD1, and that cortisol could act as a luteoprotective factor by selectively suppressing luteolytic PGF2α production in bovine endometrium.
    Type of Medium: Online Resource
    ISSN: 0022-0795 , 1479-6805
    Language: Unknown
    Publisher: Bioscientifica
    Publication Date: 2007
    detail.hit.zdb_id: 1474892-7
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