Grimes R W, Samaras S E, Hammond J M
Department of Medicine, Milton S. Hershey Medical Center, Pennsylvania State University, Hershey 17033.
Endocrinology. 1993 Mar;132(3):1414-6. doi: 10.1210/endo.132.3.7679982.
Insulin-like growth factor (IGF)-I synergizes with gonadotropin to further stimulate ovarian steroidogenesis. In contrast, the IGF-binding proteins (IGFBPs) produced by granulosa cells have been shown to antagonize the stimulatory actions of the IGFs and gonadotropins. The purpose of the present study was to examine the effects on IGFBP-3 production of prostaglandin (PG)-E2, a compound known to stimulate luteal function and prevent/delay luteal regression (a luteotropic compound), and PGF2 alpha, a compound known to be luteolytic. PGF2 alpha significantly stimulated IGFBP-3 production to 2.6-fold of control (P < 0.05) while PGE2 attenuated its production to half of control (P < 0.05). In contrast to the effects of IGFBP-3, PGE2 stimulated progesterone production to 8-fold of control (P < 0.05) while PGF2 alpha had no effect. Possible mechanisms of action of PGE2 and PGF2 alpha were also examined. PGE2, but not PGF2 alpha, stimulated cAMP accumulation which has been previously shown to inhibit IGFBP-3 production. PGF2 alpha is suspected to act via activation of protein kinase-C. However, a phorbol ester did not mimic PGF2 alpha's action toward IGFBP-3. This study demonstrated that PGE2 and PGF2 alpha conversely modulate IGFBP-3 production. Since IGFBPs have been shown to antagonize gonadotropin and IGF actions, this action of the prostaglandins may impact on the synergism between IGFs and gonadotropin necessary for follicular growth and luteal function.
胰岛素样生长因子(IGF)-I与促性腺激素协同作用,进一步刺激卵巢类固醇生成。相比之下,颗粒细胞产生的IGF结合蛋白(IGFBPs)已被证明可拮抗IGFs和促性腺激素的刺激作用。本研究的目的是检测已知能刺激黄体功能并预防/延缓黄体退化的化合物前列腺素(PG)-E2和已知具有黄体溶解作用的化合物PGF2α对IGFBP-3产生的影响。PGF2α显著刺激IGFBP-3的产生,使其达到对照的2.6倍(P<0.05),而PGE2则使其产生减少至对照的一半(P<0.05)。与IGFBP-3的作用相反,PGE2刺激孕酮产生至对照的8倍(P<0.05),而PGF2α则无作用。还研究了PGE2和PGF2α可能的作用机制。PGE2刺激了cAMP的积累,而PGF2α则没有,先前已证明cAMP积累可抑制IGFBP-3的产生。怀疑PGF2α通过蛋白激酶-C的激活发挥作用。然而,佛波酯并不能模拟PGF2α对IGFBP-3的作用。本研究表明,PGE2和PGF2α对IGFBP-3的产生具有相反的调节作用。由于IGFBPs已被证明可拮抗促性腺激素和IGF的作用,前列腺素的这种作用可能会影响卵泡生长和黄体功能所需的IGFs与促性腺激素之间的协同作用。