Brinton R D, Proffitt P, Tran J, Luu R
USC STAR Program, University of Southern California, Los Angeles 90033, USA.
Exp Neurol. 1997 Oct;147(2):211-20. doi: 10.1006/exnr.1997.6619.
Regulation of both the outgrowth and the survival of neurons involved in cognitive function can have a significant impact on the function of neural networks involved in memory and other cognitive processes. Results of this investigation demonstrated that 17beta-estradiol and the estrogenic steroids estrone, estriol, mestranol, and equilin induced significant increases in cortical nerve cell growth. Of the neurotrophic estrogenic steroids, equilin was most efficacious. We therefore conducted an extensive analysis of equilin-induced neurotrophism. Equilin induced highly significant increases in the growth of both the macro and micro features of cortical nerve cell morphology. The growth-promoting effects of equilin were present in both serum-containing and serum-free media, indicating that the growth-promoting effect of equilin is direct and not dependent upon factors present in serum. Analysis of the regional selectivity of equilin-induced neurotrophism in the cerebral cortex demonstrated that equilin significantly increased the growth of neurons from the frontal, temporal, and occipital regions, with neurons from the parietal region also influenced, though more modestly. We pursued the mechanism of equilin-induced neurotrophism and found that the growth-promoting effects of equilin were completely abolished in the presence of the glutamatergic NMDAreceptor antagonist AP5. Equilin is a major component of Premarin, the leading prescribed pharmaceutical for estrogen replacement therapy for postmenopausal women in the United States. Results of this investigation have the potential of influencing the application and design of therapeutic agents for the prevention of cognitive decline in estrogen deficient women and for the prevention of Alzheimer's disease in postmenopausal women, a group that comprises a large sector of the population, the size of which will continue to grow in the coming decades.
对参与认知功能的神经元的生长和存活进行调节,可能会对参与记忆和其他认知过程的神经网络功能产生重大影响。本研究结果表明,17β-雌二醇以及雌激素类甾体化合物雌酮、雌三醇、炔雌醇甲醚和马萘雌酮能显著促进皮质神经细胞生长。在具有神经营养作用的雌激素类甾体化合物中,马萘雌酮的效果最为显著。因此,我们对马萘雌酮诱导的神经营养作用进行了广泛分析。马萘雌酮能显著促进皮质神经细胞形态的宏观和微观特征的生长。无论在含血清培养基还是无血清培养基中,马萘雌酮均有促进生长的作用,这表明马萘雌酮的促生长作用是直接的,不依赖于血清中的因子。对马萘雌酮在大脑皮质诱导神经营养作用的区域选择性分析表明,马萘雌酮能显著促进额叶、颞叶和枕叶神经元的生长,顶叶神经元也受到影响,不过程度相对较小。我们进一步探究了马萘雌酮诱导神经营养作用的机制,发现当存在谷氨酸能N-甲基-D-天冬氨酸(NMDA)受体拮抗剂AP5时,马萘雌酮的促生长作用完全消失。马萘雌酮是倍美力的主要成分,倍美力是美国绝经后女性雌激素替代疗法中最常用的处方药。本研究结果有可能影响预防雌激素缺乏女性认知能力下降以及预防绝经后女性阿尔茨海默病的治疗药物的应用和设计,绝经后女性群体占人口的很大一部分,且在未来几十年其规模将持续增长。