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Hormone-induced luteolysis on physiologically persisting corpora lutea in Eurasian and Iberian lynx (Lynx lynx and Lynx pardinus)

机译:激素对欧亚和伊比利亚ian(Lynx lynx和Lynx pardinus)中生理上持久的黄体的黄体溶解

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The Iberian lynx (Lynx pardinus) is the most critically endangered felid. A high reproductive success within the Iberian Lynx Conservation Breeding Program is crucial to maintaining the goal of reintroducing captive born offspring to the wild and thus increasing the population. Lynx follow a unique reproductive strategy with a monoestrous cycle and persisting CLs over many years. These persistent CLs constantly produce progesterone (on average 5 ng/mL) and are hypothesized to hinder a polyestrous cyclicity in lynx. The aim of this study was to evaluate whether artificial luteolysis can be achieved with common luteolytic drugs and if luteolysis would induce a second estrus naturally. We observed a functional regression of lynx CLs after artificial luteolysis with 2.5 mu g/kg body weight PGF2 alpha analogue (cloprostenol) administered three times every 16 hours. We could see a similar effect when combining cloprostenol with other drugs like an anti-gestagen (aglepristone) or a dopamin-agonist (prolactin-inhibitor, cabergolin) or by prolonging the cloprostenol administration to a total of 5 days. However, the sample size was too small to draw conclusions about which protocol is superior or if combining different drugs would result in a positive synergism. Neither structural regression of CLs nor subsequent spontaneous estrus induction was induced with any of these treatments. We suggest that a dose of 2.5 mu g/kg body weight cloprostenol administered once daily over 3 to 5 days is sufficient for functional luteolysis in lynx. The next step would be to compare the success of estrus induction with or without the preceding artificial luteolysis
机译:伊比利亚天猫座(Lynx pardinus)是最濒危的猫科动物。伊比利亚山猫保护育种计划在生殖方面取得了巨大成功,这对于维持将圈养出生的后代重新引入野外从而增加种群的目标至关重要。天猫遵循独特的生殖策略,具有单发周期,并且持续多年的CL。这些持久性CL持续产生孕酮(平均5 ng / mL),并被认为会阻碍山猫的多发性循环。这项研究的目的是评估是否可以使用常见的溶酶药物实现人工溶酶,以及溶酶是否会自然诱发二次发情。我们观察到人工黄体溶解后,每16小时施用3次2.5μg / kg体重的PGF2α类似物(氯前列醇),从而使山猫CL的功能退化。当将氯前列醇与其他药物(例如抗孕激素(格列司通)或多巴胺激动剂(催乳素抑制剂,降钙素)合并使用或将氯前列醇的给药时间延长至总共5天时,我们可能会看到类似的效果。但是,样本量太小,无法得出关于哪种方案更好的结论,或者联合使用不同药物是否会产生积极的协同作用。这些治疗均未诱导CL的结构退化和随后的自发发情诱导。我们建议在3至5天内每天服用一次剂量为2.5μg / kg体重的氯前列腺素足以在山猫中进行功能性黄体溶解。下一步将是比较在有或没有上述人工黄体溶解的情况下发情诱导的成功

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