Yu Yuansong, Li Wei, Han Zhengbin, Luo Mingjiu, Chang Zhongle, Tan Jinghe
College of Animal Science and Veterinary Medicine, Shandong Agricultural University, Tai-an City 271018, PR China.
Theriogenology. 2003 Dec;60(9):1691-704. doi: 10.1016/j.theriogenology.2003.08.001.
The effect of FSH on goat follicular development, granulosa cell apoptosis and steroidogenesis and its mediation by insulin-like growth factor (IGF)-I were studied through both in vivo and in vitro experiments. The FSH treatment was begun on Day 9 after estrus and consisted of injections twice a day for 3 days in decreasing doses (7.5-7.5-5.0-5.0-2.5-2.5 mg). Does in both treatment and control groups were slaughtered for ovaries on Day 12. Granulosa cell apoptosis was detected by terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL). Expression of IGF-I and IGF-II mRNA was determined by RT-PCR, while concentrations of progesterone (P4), estradiol (E2), IGF-I and IGF-II were measured by radioimmunoassay (RIA). Following parameters increased significantly (P<0.05) after the FSH treatment: follicle number (5.0+/-1.5 versus 9.0+/-2.0 per ovary), the level of E2 (0.1+/-0.1 ng/ml versus 0.7+/-0.2 ng/ml), the E2/P4 ratio (0.7+/-0.4 versus 4.7+/-3.0) and the concentrations of IGF-I (0.5+/-0.2 ng/ml versus 119.4+/-15.1 ng/ml) and IGF-II (0.12+/-0.03 ng/ml versus 40.9+/-18.7 ng/ml) in follicular fluid of the medium sized (3-5 mm) follicles and in the ovarian cortex the relative quantity of IGF-I mRNA (0.37+/-0.17 versus 0.90+/-0.12 Max OD). In contrast, the ratio of apoptotic granulosa cells in these follicles was reduced significantly (0.53+/-0.1 versus 0.10+/-0.01, P<0.05). In large (>5 mm) follicles, however, only the follicle number (2.3+/-0.7 versus 7.0+/-1.5 per ovary) and the level of IGF-I (38.4+/-11.0 ng/ml versus 87.3+/-13.9 ng/ml) increased significantly (P<0.05), whereas other values did not change. In vitro culture of granulosa cells showed that FSH significantly (P<0.05) enhanced IGF-I production (12.7+/-2.1 ng/ml versus 26.+/-21.9 ng/ml) by these cells, and both FSH and IGF-I reduced the ratios of apoptotic cells (from 0.7+/-0.07 to 0.3+/-0.1 and 0.2+/-0.04, respectively) and the effect was additive when both were used together. H89, the PKA pathway inhibitor, blocked the effect of FSH on granulosa cell apoptosis and IGF-I production in vitro. These results indicated that FSH mainly enhanced the development of medium sized follicles in the goat by suppressing the apoptosis of granulosa cells via increasing production of IGF-I and steroids, possibly through the PKA pathway.
通过体内和体外实验研究了促卵泡素(FSH)对山羊卵泡发育、颗粒细胞凋亡和类固醇生成的影响及其通过胰岛素样生长因子(IGF)-I介导的作用。FSH处理在发情后第9天开始,连续3天每天注射2次,剂量递减(7.5 - 7.5 - 5.0 - 5.0 - 2.5 - 2.5毫克)。在第12天对处理组和对照组的母羊屠宰取卵巢。通过末端脱氧核苷酸转移酶介导的dUTP缺口末端标记法(TUNEL)检测颗粒细胞凋亡。通过逆转录聚合酶链反应(RT-PCR)测定IGF-I和IGF-II mRNA的表达,同时通过放射免疫测定法(RIA)测量孕酮(P4)、雌二醇(E2)、IGF-I和IGF-II的浓度。FSH处理后,以下参数显著增加(P<0.05):卵泡数量(每个卵巢5.0±1.5个对9.0±2.0个)、E2水平(0.1±0.1纳克/毫升对0.7±0.2纳克/毫升)、E2/P4比值(0.7±0.4对4.7±3.0)以及中等大小(3 - 5毫米)卵泡卵泡液中IGF-I(0.5±0.2纳克/毫升对119.4±15.1纳克/毫升)和IGF-II(0.12±0.03纳克/毫升对40.9±18.7纳克/毫升)的浓度,以及卵巢皮质中IGF-I mRNA的相对量(0.37±0.17对0.90±0.12最大光密度)。相反,这些卵泡中凋亡颗粒细胞的比例显著降低(0.53±0.1对0.10±0.01,P<0.05)。然而,在大卵泡(>5毫米)中,只有卵泡数量(每个卵巢2.3±0.7个对7.0±1.5个)和IGF-I水平(38.4±11.0纳克/毫升对87.3±13.9纳克/毫升)显著增加(P<0.05),而其他值没有变化。颗粒细胞的体外培养表明,FSH显著(P<0.05)增强了这些细胞的IGF-I产生(12.7±2.1纳克/毫升对26.±(此处原文有误,应为26.0±)21.9纳克/毫升),并且FSH和IGF-I都降低了凋亡细胞的比例(分别从0.7±0.07降至0.3±0.1和0.2±0.04),当两者一起使用时效果是相加的。PKA途径抑制剂H89阻断了FSH对体外颗粒细胞凋亡和IGF-I产生的作用。这些结果表明,FSH主要通过增加IGF-I和类固醇的产生,可能通过PKA途径抑制颗粒细胞凋亡,从而促进山羊中等大小卵泡的发育。