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PGF2α 在黄体溶解中的作用基于对母马 PGF2α 合成的抑制。

Role of PGF2α in luteolysis based on inhibition of PGF2α synthesis in the mare.

机构信息

Eutheria Foundation, Cross Plains, Wisconsin, USA; ICAAM-Instituto de Ciências Agrárias e Ambientais Mediterrânicas, Department of Veterinary Medicine, Escola de Ciências e Tecnologia, Universidade de Évora, Núcleo da Mitra, Évora, Portugal; Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, Wisconsin, USA.

出版信息

Theriogenology. 2013 Oct 15;80(7):812-20. doi: 10.1016/j.theriogenology.2013.07.008. Epub 2013 Aug 13.

Abstract

The effects of inhibition of PGF2α synthesis on luteolysis in mares and on the incidence of prolonged luteal activity were studied in controls and in a group treated with flunixin meglumine (FM), a PGF2α inhibitor (n = 6/group). The FM was given every 8 hours (1.0 mg/kg) on each of Days 14.0 to 16.7. Concentration (pg/mL) of PGF2α metabolite averaged over 8 hours of hourly blood sampling at the beginning of each day, was lower in the FM group than in the controls on Day 14 after ovulation (6.7 ± 1.3 vs. 13.8 ± 2.9, P < 0.05), Day 15 (15.0 ± 3.9 vs. 35.2 ± 10.4, P < 0.10), and Day 16 (21.9 ± 5.7 vs. 54.7 ± 11.4, P < 0.03). Concentration (ng/mL) of progesterone (P4) was greater in the FM group than in the controls on Day 14 (10.1 ± 0.9 vs. 7.7 ± 0.9, P < 0.08), Day 15 (9.2 ± 1.0 vs. 4.3 ± 1.0, P < 0.008), and Day 16 (5.6 ± 1.6 vs. 1.2 ± 0.4, P < 0.02). The interval from ovulation to the beginning of a decrease in P4 and to the end of luteolysis (P4 < 1 ng/mL) was each delayed (P < 0.03) by ~1 day in the FM group. Intervals involving the luteal phase were long (statistical outliers, P < 0.05) in two mares in the FM group, indicating prolonged luteal activity. Results supported the hypotheses that (1) inhibition of PGF2α synthesis interferes with luteolysis in mares and (2) inhibition of PGF2α at the expected time of luteolysis may lead to prolonged luteal activity.

摘要

本研究旨在探讨抑制 PGF2α 合成对马黄体溶解及延长黄体活动时间的影响,试验选用对照组和氟尼辛甲胺(PGF2α 抑制剂)治疗组(每组 6 匹马)进行。FM 于发情周期第 14.0 天至第 16.7 天,每天 8 小时(1.0 mg/kg)肌肉注射。每天开始时每 8 小时采集 1 小时血样,计算平均 8 小时内 PGF2α 代谢产物浓度。与对照组相比,发情周期第 14 天排卵后(6.7±1.3 vs. 13.8±2.9,P<0.05)、第 15 天(15.0±3.9 vs. 35.2±10.4,P<0.10)和第 16 天(21.9±5.7 vs. 54.7±11.4,P<0.03),FM 组的平均 8 小时内 PGF2α 代谢产物浓度较低。FM 组孕酮(P4)浓度高于对照组,发情周期第 14 天(10.1±0.9 vs. 7.7±0.9,P<0.08)、第 15 天(9.2±1.0 vs. 4.3±1.0,P<0.008)和第 16 天(5.6±1.6 vs. 1.2±0.4,P<0.02)。FM 组从排卵到 P4 开始下降和黄体溶解结束(P4<1ng/mL)的时间间隔分别延迟了约 1 天(P<0.03)。FM 组有 2 匹母马的黄体期时间较长(统计学异常值,P<0.05),表明黄体活动延长。结果表明,(1)抑制 PGF2α 合成会干扰马的黄体溶解;(2)在黄体溶解的预期时间抑制 PGF2α 可能导致黄体活动延长。

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