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Effects of leptin administration and feed restriction on thecal leucocytes in the preovulatory rat ovary and the effects of leptin on meiotic maturation, granulosa cell proliferation, steroid hormone and PGE2 release in cultured rat ovarian follicles

机译:瘦素给药和饲料限制对排卵前期大鼠卵巢白细胞的影响及瘦素对培养大鼠卵巢卵母细胞减数分裂成熟,颗粒细胞增殖,类固醇激素和pGE2释放的影响

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摘要

Leptin is expressed by adipocytes and is thought to play a role in regulating food intake and in reproduction. It has been demonstrated that acute leptin administration to immature gonadotrophin-primed rats in vivo inhibits ovulation and causes a decline in food intake. However, feed restriction alone does not inhibit ovulation. Two experiments were designed to investigate the mechanism of leptin-induced inhibition of ovulation. In the first experiment, which was prompted by the importance of ovarian leucocytes in ovulation, the role of leucocytes in leptin-induced inhibition of ovulation was investigated. The second experiment investigated whether high leptin concentrations could inhibit other factors important to ovulation, such as meiotic competence of oocytes, granulosa cell proliferation, steroid or PGE(2) release, and interleukin 1beta production, in vitro. In the first experiment, the populations of neutrophils and monocytes-macrophages in the preovulatory follicles of gonadotrophin-primed, leptin-treated and -untreated rats were examined. A decrease in food intake, as a result of either leptin treatment or feed restriction, specifically reduced the numbers of neutrophils and monocytes-macrophages infiltrating the theca interna of preovulatory follicles without affecting the numbers found in the stroma. The findings show that reduced infiltration of thecal neutrophils and macrophages into preovulatory follicles is a response to reduced food intake. Furthermore, this reduction is not the direct cause of the leptin-induced inhibition of ovulation. In the second experiment, ovarian follicles were cultured for 4 or 12 h in the presence or absence of the following hormones: FSH (500 miu), insulin-like growth factor I (IGF-I) (50 ng ml(-1)), LH (100 ng ml(-1)) and leptin (300 ng ml(-1)). The results demonstrated that high concentrations of leptin in follicle culture do not affect meiotic maturation or steroid release, but tend to inhibit release of PGE 2 (although this result was not significant). DNA synthesis in granulosa cells was not inhibited by leptin in FSH- and IGF-I-supplemented culture media. These results are in agreement with previous studies that have shown that leptin inhibits the stimulatory effects of IGF-I on FSH-stimulated oestradiol production in rat granulosa cells without affecting progesterone production. In summary, leptin does not appear to have an adverse effect on the components of ovulation tested in this study, and therefore must impact on the ovulatory cascade in a way that remains to be defined.
机译:瘦素由脂肪细胞表达,被认为在调节食物摄入和繁殖中发挥作用。已经证明,在体内对未成熟的促性腺激素引发的大鼠急性施用瘦蛋白会抑制排卵并导致食物摄入减少。但是,仅限制采食不会抑制排卵。设计了两个实验来研究瘦素诱导的排卵抑制机制。在第一个实验中,卵巢中的白细胞在排卵中的重要性提示了这一点,研究了白细胞在瘦素诱导的排卵抑制中的作用。第二个实验研究了高瘦素浓度是否可以抑制其他对排卵重要的因素,例如卵母细胞的减数分裂能力,颗粒细胞增殖,类固醇或PGE(2)释放以及白介素1β的产生。在第一个实验中,检查了促性腺激素引发,瘦素治疗和未治疗的大鼠排卵前卵泡中嗜中性粒细胞和单核细胞巨噬细胞的种群。瘦素治疗或饲料限制导致的食物摄入减少,特别是减少了排卵前卵泡内膜中性粒细胞和单核细胞-巨噬细胞的数量,而不会影响基质中的数量。研究结果表明,减少中性粒细胞和巨噬细胞渗入排卵前卵泡是对食物摄入减少的一种反应。此外,这种减少不是瘦素诱导的排卵抑制的直接原因。在第二个实验中,在以下激素存在或不存在的情况下,将卵泡培养4或12 h:FSH(500 miu),胰岛素样生长因子I(IGF-I)(50 ng ml(-1)) ,LH(100 ng ml(-1))和瘦素(300 ng ml(-1))。结果表明,卵泡培养物中高浓度的瘦素不会影响减数分裂成熟或类固醇释放,但会抑制PGE 2的释放(尽管这一结果并不明显)。在补充了FSH和IGF-I的培养基中,瘦素不会抑制颗粒细胞中的DNA合成。这些结果与以前的研究一致,后者表明瘦素抑制了IGF-1对大鼠颗粒细胞中FSH刺激的雌二醇产生的刺激作用,而不会影响孕酮的产生。总之,瘦素似乎对本研究中测试的排卵成分没有不利影响,因此必须以尚待确定的方式影响排卵期。

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