Hsueh A J, Liu Y X, Cajander S, Peng X R, Dahl K, Kristensen P, Ny T
Department of Reproductive Medicine, University of California-San Diego, La Jolla 92093.
Endocrinology. 1988 Apr;122(4):1486-95. doi: 10.1210/endo-122-4-1486.
GnRH and its agonists are known to induce ovulation in hypophysectomized rats by acting directly at the ovary. Because tissue-type plasminogen activator (tPA) has been implicated in the gonadotropin induction of ovulation, we examined the effect of an ovulatory dose of GnRH on ovarian tPA activity, mRNA content, and cellular localization. Hypophysectomized immature rats were injected sc with 20 IU PMSG and a single dose of a GnRH agonist (GnRHa; des-Gly10,DLeu6(N alpha Me)Leu7,Pro9NHEt-GnRH) 58 h later. At different times after treatment, ovaries were prepared for morphological analysis. Using a fibrin overlay method, tPA activities were measured in ovarian homogenates and cumulus-oocyte complexes, whereas granulosa cells were cultured for 24 h to estimate tPA secretion. Total ovarian RNA was prepared for hybridization analysis of tPA message levels, and tPA localization was studied by immunohistochemistry of ovarian sections. GnRHa induced ovulation in PMSG-primed hypophysectomized rats 14-16 h after injection in a dose-dependent manner, and the GnRHa action was blocked by concomitant treatment with a GnRH antagonist. GnRHa stimulated the induction of tPA, but not urokinase-type PA, activity in ovarian homogenates and granulosa cell-conditioned medium in a time-dependent manner, reaching a maximum before ovulation. tPA activity in cumulus-oocyte complexes was also increased before ovulation, but this increase was sustained. Hybridization analysis of steady state tPA mRNA levels was performed using a rat cRNA probe. Northern blot analysis of total ovarian RNA demonstrated that GnRHa stimulated tPA mRNA levels 12 h after treatment, with a subsequent decrease 24 h after treatment. Immunohistochemistry indicated substantial increases in tPA staining in granulosa cells and oocytes of preovulatory follicles before ovulation. Thus, GnRHa acts through specific receptors to increase ovarian tPA enzyme activity, mRNA content, as well as immunostaining in granulosa cells and oocytes. Like gonadotropins, GnRH may induce ovulation by directly stimulating tPA levels in the ovary.
已知促性腺激素释放激素(GnRH)及其激动剂通过直接作用于卵巢,可诱导垂体切除的大鼠排卵。由于组织型纤溶酶原激活物(tPA)与促性腺激素诱导的排卵有关,我们研究了排卵剂量的GnRH对卵巢tPA活性、mRNA含量及细胞定位的影响。对垂体切除的未成熟大鼠皮下注射20 IU孕马血清促性腺激素(PMSG),58小时后注射单剂量的GnRH激动剂(GnRHa;去甘氨酸10、D -亮氨酸6(Nα -甲基)亮氨酸7、脯氨酸9 - N -乙基 - GnRH)。在治疗后的不同时间,制备卵巢用于形态学分析。采用纤维蛋白覆盖法,测定卵巢匀浆和卵丘 - 卵母细胞复合体中的tPA活性,同时培养颗粒细胞24小时以评估tPA分泌。制备卵巢总RNA用于tPA信息水平的杂交分析,并通过卵巢切片的免疫组织化学研究tPA定位。GnRHa以剂量依赖的方式在注射后14 - 16小时诱导PMSG预处理的垂体切除大鼠排卵,且GnRHa的作用可被同时使用的GnRH拮抗剂阻断。GnRHa以时间依赖的方式刺激卵巢匀浆和颗粒细胞条件培养基中tPA而非尿激酶型PA的活性诱导,在排卵前达到最大值。卵丘 - 卵母细胞复合体中的tPA活性在排卵前也增加,但这种增加持续存在。使用大鼠cRNA探针进行稳态tPA mRNA水平的杂交分析。对卵巢总RNA的Northern印迹分析表明,GnRHa在治疗后12小时刺激tPA mRNA水平,随后在治疗后24小时下降。免疫组织化学表明,排卵前卵泡的颗粒细胞和卵母细胞中tPA染色在排卵前显著增加。因此,GnRHa通过特异性受体发挥作用,增加卵巢tPA酶活性、mRNA含量以及颗粒细胞和卵母细胞中的免疫染色。与促性腺激素一样,GnRH可能通过直接刺激卵巢中的tPA水平来诱导排卵。