Bonello N P, Norman R J, Brännström M
Reproductive Medicine Unit, Department of Obstetrics and Gynaecology, The University of Adelaide, The Queen Elizabeth Hospital, 5011, Woodville, South Australia, Australia.
Endocrine. 1995 Jan;3(1):49-54. doi: 10.1007/BF02917448.
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.
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。