Greisen S, Ledet T, Møller N, Jørgensen J O, Christiansen J S, Petersen K, Ovesen P
Department of Gynecology and Obstetrics, Aarhus University Hospital, Denmark.
Acta Obstet Gynecol Scand. 2000 Nov;79(11):931-5.
Body weight influences fertility and studies in mice have indicated that leptin is one of the mediators of this effect. Leptin is believed to centrally stimulate the hypothalamic-pituitary axis resulting in increased gonadotropin release. Moreover, leptin is present in follicular fluid and the receptor is expressed in the human ovary. The aim of this study was to evaluate the direct effect of leptin on cultured human granulosa cell steroidogenesis.
Granulosa cells were obtained in connection with IVF procedures, and then cultured in a serum-free medium containing androstenedione (1 microM) for a total of 4 days. After 2 days of culture the medium was changed and the hormones under study were added. We tested the effect of leptin (1, 20, 100 ng/ml) on basal, FSH (10-100 ng/ml), and FSH (10-100 ng/ml)+IGF-I (30 ng/ml) stimulated steroidogenesis.
Leptin (20 ng/ml and 100 ng/ml) significantly reduced basal and FSH-stimulated estradiol secretion (p<0.05). Basal and FSH (10 and 30 ng/ml) stimulated progesterone production was significantly inhibited by leptin 20 ng/ml, whereas leptin 100 ng/ml significantly reduced basal but not FSH stimulated progesterone production. Finally, steroidogenesis stimulated by IGF-I alone and in combination with FSH was not influenced by leptin.
These results suggest that leptin acts directly to inhibit basal and FSH stimulated estradiol and progesterone production in cultured human granulosa cells. This raises the possibility that high circulating leptin levels as seen in obese women may compromise fertility through peripheral mechanisms.
体重会影响生育能力,小鼠研究表明瘦素是这种作用的介质之一。瘦素被认为可在下丘脑-垂体轴发挥中枢刺激作用,从而导致促性腺激素释放增加。此外,卵泡液中存在瘦素,且其受体在人类卵巢中表达。本研究的目的是评估瘦素对培养的人颗粒细胞类固醇生成的直接影响。
在体外受精过程中获取颗粒细胞,然后在含有雄烯二酮(1微摩尔)的无血清培养基中培养4天。培养2天后更换培养基并添加研究中的激素。我们测试了瘦素(1、20、100纳克/毫升)对基础状态、促卵泡激素(10 - 100纳克/毫升)以及促卵泡激素(10 - 100纳克/毫升)+胰岛素样生长因子-I(30纳克/毫升)刺激的类固醇生成的影响。
瘦素(20纳克/毫升和100纳克/毫升)显著降低基础状态和促卵泡激素刺激的雌二醇分泌(p<0.05)。20纳克/毫升的瘦素显著抑制基础状态以及促卵泡激素(10和30纳克/毫升)刺激的孕酮生成,而100纳克/毫升的瘦素显著降低基础状态但不影响促卵泡激素刺激的孕酮生成。最后,单独胰岛素样生长因子-I以及胰岛素样生长因子-I与促卵泡激素联合刺激的类固醇生成不受瘦素影响。
这些结果表明,瘦素直接作用于培养的人颗粒细胞,抑制基础状态和促卵泡激素刺激的雌二醇和孕酮生成。这增加了肥胖女性中所见的高循环瘦素水平可能通过外周机制损害生育能力的可能性。