Peluso J J, Luttmer S, Gruenberg M L
J Reprod Fertil. 1984 Sep;72(1):173-7. doi: 10.1530/jrf.0.0720173.
Three to four ovaries from rats on the day of di-oestrus I were placed in perifusion culture at 10:30 h and exposed to (1) no gonadotrophin (in-vitro controls); (2) tonic FSH (200 ng RP-1/ml); (3) tonic LH (30 ng RP-1/ml); (4) tonic FSH + tonic LH; or (5) tonic FSH plus hourly pulses of LH (amplitude = 50 ng/ml). The total amount of LH administered was 3060 ng RP-1 regardless of mode of delivery. After culture for 3 h, the ovaries were prepared for histological analysis. Compared to in-vitro controls, tonic LH stimulation increased the number of follicles with greater than 1.6 X 10(5) granulosa cells (P less than 0.05); it was estimated that each follicle in the larger size class increased by 5.5 +/- 2.7 X 10(4) cells. Tonic FSH or tonic FSH + tonic LH treatment did not promote growth into the 1.6 X 10(5) cell class. In the presence of tonic FSH, hourly LH pulses induced follicular growth similar to that observed after tonic LH treatment. The data demonstrate that LH promotes the growth of follicles in vitro. FSH modulates this stimulatory action of LH, allowing it to be expressed when LH is administered in hourly pulses.
在动情间期第一天,从大鼠体内取出三到四个卵巢,于上午10:30进行灌流培养,并分别暴露于以下环境:(1) 无促性腺激素(体外对照);(2) 持续性促卵泡激素(200 ng RP-1/ml);(3) 持续性促黄体生成素(30 ng RP-1/ml);(4) 持续性促卵泡激素 + 持续性促黄体生成素;或(5) 持续性促卵泡激素加每小时一次的促黄体生成素脉冲(幅度 = 50 ng/ml)。无论给药方式如何,促黄体生成素的给药总量均为3060 ng RP-1。培养3小时后,对卵巢进行组织学分析。与体外对照相比,持续性促黄体生成素刺激增加了颗粒细胞数量大于1.6×10⁵的卵泡数量(P < 0.05);据估计,较大尺寸类别的每个卵泡增加了5.5±2.7×10⁴个细胞。持续性促卵泡激素或持续性促卵泡激素 + 持续性促黄体生成素处理并未促进卵泡生长至1.6×10⁵细胞类别。在存在持续性促卵泡激素的情况下,每小时一次的促黄体生成素脉冲诱导的卵泡生长与持续性促黄体生成素处理后观察到的相似。数据表明,促黄体生成素在体外促进卵泡生长。促卵泡激素调节促黄体生成素的这种刺激作用,使其在每小时给予促黄体生成素脉冲时得以表达。