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白细胞介素-1β在体外抑制大鼠排卵前卵泡中促黄体生成素诱导的纤溶酶原激活物活性。

Interleukin-1β inhibits luteinizing hormone-induced plasminogen activator activity in rat preovulatory folliclesin vitro.

作者信息

Bonello N P, Norman R J, Brännström M

机构信息

Reproductive Medicine Unit, Department of Obstetrics and Gynaecology, The University of Adelaide, The Queen Elizabeth Hospital, 5011, Woodville, South Australia, Australia.

出版信息

Endocrine. 1995 Jan;3(1):49-54. doi: 10.1007/BF02917448.

Abstract

The effects of interleukin-1β (IL-1β) and tumour necrosis factor-α (TNFα) on ovulation-associated plasminogen activator (PA) activity were investigated using preovulatory follicles excised 48h after equine chorionic gonadotrophin (16IU)-priming of immature rats. Follicles were incubated for 6 and 14h with a single dose of LH (1 μg/ml) only, or various cytokine doses in the presence or absence of LH. PA activity in follicular homogenates was determined by a radioactively labelled fibrin-coated plate method and secreted levels of the ovulatory mediators progesterone (P) and prostaglandin E (PGE) were measured by radioimmunoassay. LH induced timedependent rises in PA (2.5-fold over control at 6h and fourfold over control at 14h), while IL-1β and TNFα alone had no effect over either time period. LH and cytokine coincubations over 14h revealed that IL-1β dosedependently inhibited the LH-induced increase in PA activity, up to 85%. The effects of TNFα on LH-induced PA activity were not significant. Both IL-1β and TNFα increased P and PGE secretion time- and dose-dependently. In summary, IL-1β dose-dependently inhibits the LH-induced increase in PA activity in rat preovulatory folliclesin vitro while, as with TNFα, increasing P and PGE synthesis. This study, shows that the earlier reported pro-ovulatory action of IL-1β is not likely to be mediated by activation of the PA-system and suggests that IL-1β may mediate a regulatory loop controlling the extent and distribution of LH-induced PA activity in rat preovulatory follicles.

摘要

利用未成熟大鼠经马绒毛膜促性腺激素(16IU)预处理48小时后切除的排卵前卵泡,研究白细胞介素-1β(IL-1β)和肿瘤坏死因子-α(TNFα)对排卵相关纤溶酶原激活物(PA)活性的影响。卵泡分别单独用单剂量促黄体生成素(LH,1μg/ml)孵育6小时和14小时,或在有或无LH存在的情况下与不同剂量的细胞因子一起孵育。通过放射性标记的纤维蛋白包被平板法测定卵泡匀浆中的PA活性,并通过放射免疫分析法测量排卵介质孕酮(P)和前列腺素E(PGE)的分泌水平。LH诱导PA活性随时间依赖性升高(6小时时比对照高2.5倍,14小时时比对照高4倍),而单独的IL-1β和TNFα在两个时间段均无影响。LH与细胞因子共同孵育14小时显示,IL-1β剂量依赖性地抑制LH诱导的PA活性增加,最高可达85%。TNFα对LH诱导的PA活性的影响不显著。IL-1β和TNFα均能时间和剂量依赖性地增加P和PGE的分泌。总之,IL-1β在体外剂量依赖性地抑制大鼠排卵前卵泡中LH诱导的PA活性增加,而与TNFα一样,能增加P和PGE的合成。本研究表明,先前报道的IL-1β的促排卵作用不太可能通过PA系统的激活介导,并提示IL-1β可能介导一个调节环路,控制大鼠排卵前卵泡中LH诱导的PA活性的程度和分布。

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