Ferrero P, Rocca P, Montalenti E, Benna P, Milani A, Ravizza L, Bergamasco B
Department of Neurology, University of Turin, Italy.
Psychoneuroendocrinology. 1994;19(1):65-78. doi: 10.1016/0306-4530(94)90060-4.
Peripheral-type benzodiazepine receptors (pBZr) have been shown to be sensitive to hormonal perturbations, including changes in ovarian steroids. This study examines whether estradiol and progesterone modulate pBZr binding in membranes of human blood mononuclear cells, as measured by binding of both 3H-PK 11195 and 3H-Ro 5-4864. Our findings were negative. There was no steroidal modulation of pBZr binding to these membrane preparations in vivo in normal women studied at different sex-steroid phases of the menstrual cycle, or during 8-30 weeks of pregnancy. There was also no effect of hormones on the binding sites in cultures of mononuclear cells treated with estradiol or progesterone (up to 10(-5) M) over a period between 2 and 72 h. Further, we performed in vitro competition experiments, which showed that both steroids are not active at the pBZr. Our data suggest that pBZr located in human blood mononuclear cells are insensitive to the physiological variations of circulating female hormones.
外周型苯二氮䓬受体(pBZr)已被证明对激素紊乱敏感,包括卵巢甾体激素的变化。本研究通过3H-PK 11195和3H-Ro 5-4864的结合来检测雌二醇和孕酮是否调节人血单核细胞膜中pBZr的结合。我们的研究结果为阴性。在月经周期不同性甾体阶段研究的正常女性体内,或在妊娠8至30周期间,pBZr与这些膜制剂的结合没有甾体调节作用。在用雌二醇或孕酮(高达10^(-5) M)处理2至72小时的单核细胞培养物中,激素对结合位点也没有影响。此外,我们进行了体外竞争实验,结果表明这两种甾体在pBZr处均无活性。我们的数据表明,位于人血单核细胞中的pBZr对循环女性激素的生理变化不敏感。