Luquin S, Naftolin F, Garcia-Segura L M
Instituto Cajal, C.S.I.C., Madrid, Spain.
J Neurobiol. 1993 Jul;24(7):913-24. doi: 10.1002/neu.480240705.
The number and the surface density of cells immunoreactive for the specific astrocytic marker glial fibrillary acidic protein (GFAP), were evaluated in both the hilus of the dentate gyrus and the granular layer of the vermis of the cerebellar cortex of adult female rats during the different phases of the estrous cycle, after ovariectomy and after the pharmacological administration of estradiol and/or progesterone to ovariectomized rats. Although no significant differences were detected in the number of immunoreactive cells among the different experimental groups studied, their surface density showed significant changes in the hilus of the dentate gyrus. The surface density of immunoreactive cells was increased in the afternoon of proestrus and on the morning of estrus compared to the morning of proestrus, diestrus, and metestrus, was decreased after ovariectomy, and showed a dose-dependent increase in ovariectomized rats injected with 17 beta estradiol (1, 10, or 300 micrograms/rat), alone or in combination with progesterone (500 micrograms/rat). In contrast, it was not affected by the administration of 17 alpha estradiol (300 micrograms/rat). The surface density of immunoreactive cells was significantly increased over control values by 5 h after the injection of 17 beta estradiol (300 micrograms/rat) and as early as 1 h after the administration of progesterone. The separate injection of either 17 beta estradiol or progesterone had smaller effects on the surface density of immunoreactive cells than did the administration of both hormones together. The surface density of GFAP-immunoreactive cells reached maximal values by 24 h after the administration of 17 beta estradiol and/or progesterone and returned to control levels by 48 h after the combined injection of progesterone and 17 beta estradiol, while in the rats that were injected with only one of the two hormones, the surface density of immunoreactive cells remained over control values for at least 9 days. No such hormonal effects on GFAP-immunoreactive cells were observed in the cerebellar cortex.
在成年雌性大鼠发情周期的不同阶段、卵巢切除术后以及对卵巢切除的大鼠进行雌二醇和/或孕酮药物给药后,评估了对特定星形胶质细胞标志物胶质纤维酸性蛋白(GFAP)免疫反应阳性的细胞数量和表面密度。在齿状回的门区和小脑皮质蚓部的颗粒层进行评估。尽管在所研究的不同实验组之间未检测到免疫反应阳性细胞数量的显著差异,但它们在齿状回门区的表面密度显示出显著变化。与发情前期、动情后期和间情期的早晨相比,发情前期下午和发情期早晨免疫反应阳性细胞的表面密度增加,卵巢切除术后降低,并且在单独或与孕酮(500微克/大鼠)联合注射17β-雌二醇(1、10或300微克/大鼠)的卵巢切除大鼠中呈剂量依赖性增加。相比之下,注射17α-雌二醇(300微克/大鼠)对其没有影响。注射17β-雌二醇(300微克/大鼠)后5小时,免疫反应阳性细胞的表面密度比对照值显著增加,而在给予孕酮后1小时就已显著增加。单独注射17β-雌二醇或孕酮对免疫反应阳性细胞表面密度的影响小于两种激素联合给药的影响。给予17β-雌二醇和/或孕酮后24小时,GFAP免疫反应阳性细胞的表面密度达到最大值,在联合注射孕酮和17β-雌二醇后48小时恢复到对照水平,而在仅注射两种激素之一的大鼠中,免疫反应阳性细胞的表面密度至少9天保持在对照值之上。在小脑皮质中未观察到对GFAP免疫反应阳性细胞的此类激素作用。