Negishi H, Furuta I, Ushigoe K, Fujimoto S, Koide S S
Dept. of Obstetrics and Gynecology, Hokkaido University School of Medicine, Sapporo, Japan.
Endocr Res. 1998 May;24(2):195-203. doi: 10.1080/07435809809135528.
Cabergoline (CG), a dopamine agonist, and prolactin (PRL) added in vitro to isolated granulosa cells from immature rats cultured in serum-free medium inhibited FSH-stimulated production of progesterone. The lowest effective concentrations of CG and PRL were 10(-8)M and 1 ng/mL, respectively. In combination, the inhibitory activities were additive. CG at 10(-8) M also suppressed estradiol production by isolated rat granulosa cells; whereas PRL did not. In conclusion, CG inhibits FSH-stimulated progesterone and estradiol production by rat granulosa cells.
卡麦角林(CG)是一种多巴胺激动剂,在体外将其与催乳素(PRL)添加到在无血清培养基中培养的未成熟大鼠分离的颗粒细胞中,可抑制促卵泡激素(FSH)刺激的孕酮生成。CG和PRL的最低有效浓度分别为10^(-8)M和1 ng/mL。联合使用时,抑制活性具有相加性。10^(-8) M的CG也可抑制分离的大鼠颗粒细胞的雌二醇生成;而PRL则不能。总之,CG可抑制FSH刺激的大鼠颗粒细胞孕酮和雌二醇生成。