Murray J F, Downing J A, Evans G, Findlay J K, Scaramuzzi R J
Department of Animal Science, University of Sydney, New South Wales, Australia.
J Endocrinol. 1993 May;137(2):253-64. doi: 10.1677/joe.0.1370253.
Epidermal growth factor (EGF) is a potential intra-ovarian modulator of gonadotroph action on differentiated follicular cells. Specific binding sites have been identified in the ovary and functional differentiation in cultured granulosa cells can be modulated by treatment with EGF. The aim of this study was to determine if EGF was capable of altering ovarian function in vivo during the follicular phase of the sheep oestrous cycle. Fourteen cross-bred ewes with ovarian autotransplants were treated with progestagen pessaries for 12 days. Three ewes were infused with murine EGF (mEGF) via the jugular vein (75 micrograms/kg bodyweight per 12 h) during the 12 h preceding progestagen pessary withdrawal, and received an injection of a prostaglandin analogue at 0 h to induce luteolysis. Over the same time-period, two doses of EGF were administered to other groups of ewes by infusion into the ovarian artery (low: 6 micrograms/12 h, n = 3 and high: 60 micrograms/12 h, n = 3). The remaining five ewes were not infused with EGF (controls). Jugular and ovarian venous blood samples were taken at 10-min intervals at two stages during the follicular phase (21-27 h and 38-42 h after pessary withdrawal) and every 2 h from 44 to 76 or 86 h. mEGF, LH, FSH, inhibin, androstenedione, oestradiol-17 beta and progesterone concentrations in plasma were determined using radioimmunoassays. The secretion rates of androstenedione, oestradiol, progesterone and inhibin by the ovary were calculated. EGF acted directly on the ovary in a dose-dependent manner. Oestradiol secretion was inhibited following treatment with EGF but androstenedione secretion was unaffected. EGF appears therefore to act within the granulosa cells to inhibit aromatization. Inhibin secretion was also suppressed by treatment with EGF, though it was not possible to determine if this was caused by a direct or indirect action of EGF on granulosa cells. The rate of progesterone secretion increased in ewes receiving systemic (i.e. via the jugular vein) and high-dose intra-arterial infusions of EGF, even though a preovulatory LH surge was not observed in these animals during the entire experimental period. Concomitant increases in both LH and FSH secretion were associated with these effects of EGF on ovarian function. In conclusion, EGF appears to act directly on the granulosa cells of the follicle to inhibit aromatization and also to inhibit inhibin production. The low levels of oestradiol and inhibin in the presence of high levels of gonadotrophin indicate that atresia may have been induced in medium to large antral follicles.(ABSTRACT TRUNCATED AT 400 WORDS)
表皮生长因子(EGF)是促性腺激素作用于分化卵泡细胞时卵巢内潜在的调节因子。已在卵巢中鉴定出特异性结合位点,并且用EGF处理可调节培养的颗粒细胞的功能分化。本研究的目的是确定EGF在绵羊发情周期的卵泡期是否能够在体内改变卵巢功能。十四只进行了卵巢自体移植的杂种母羊用孕酮阴道栓处理12天。三只母羊在孕酮阴道栓取出前12小时通过颈静脉注入鼠表皮生长因子(mEGF)(每12小时75微克/千克体重),并在0小时注射前列腺素类似物以诱导黄体溶解。在同一时间段内,通过注入卵巢动脉向其他组母羊给予两剂EGF(低剂量:6微克/12小时,n = 3;高剂量:60微克/12小时,n = 3)。其余五只母羊未注入EGF(对照组)。在卵泡期的两个阶段(取出阴道栓后21 - 27小时和38 - 42小时)每隔10分钟采集颈静脉和卵巢静脉血样,并在44至76或86小时期间每2小时采集一次。使用放射免疫测定法测定血浆中的mEGF、促黄体生成素(LH)、促卵泡生成素(FSH)、抑制素、雄烯二酮、雌二醇 - 17β和孕酮浓度。计算卵巢分泌雄烯二酮、雌二醇、孕酮和抑制素的速率。EGF以剂量依赖的方式直接作用于卵巢。用EGF处理后雌二醇分泌受到抑制,但雄烯二酮分泌未受影响。因此,EGF似乎在颗粒细胞内起作用以抑制芳香化作用。用EGF处理也抑制了抑制素的分泌,尽管无法确定这是由EGF对颗粒细胞的直接作用还是间接作用引起的。接受全身性(即通过颈静脉)和高剂量动脉内注入EGF的母羊孕酮分泌速率增加,尽管在整个实验期间这些动物未观察到排卵前促黄体生成素高峰。EGF对卵巢功能的这些影响伴随着促黄体生成素和促卵泡生成素分泌的同时增加。总之,EGF似乎直接作用于卵泡的颗粒细胞以抑制芳香化作用并抑制抑制素的产生。在促性腺激素水平高的情况下雌二醇和抑制素水平低表明中到大的窦状卵泡可能已被诱导闭锁。(摘要截短至400字)