McEwen B S, Alves S E, Bulloch K, Weiland N G
Harold and Margaret Hatch Laboratory of Neuroendocrinology, Rockefeller University, New York, NY 10021, USA.
Neurology. 1997 May;48(5 Suppl 7):S8-15. doi: 10.1212/wnl.48.5_suppl_7.8s.
Ovarian steroids have many effects on the brain throughout the lifespan, beginning during gestation and continuing into senescence. These hormones affect areas of the brain that are not primarily involved in reproduction, such as the basal forebrain, hippocampus, caudate putamen, midbrain raphe, and brainstem locus coeruleus. Here we discuss three effects of estrogens and progestins that are especially relevant to memory processes and identify hormonal alterations associated with aging and neurodegenerative diseases. First, estrogens and progestins regulate synaptogenesis in the CA1 region of the hippocampus during the 4- to 5-day estrous cycle of the female rat. Formation of new excitatory synapses is induced by estradiol and involves N-methyl-D-aspartate (NMDA) receptors, whereas synaptic downregulation involves intracellular progestin receptors. Second, there are developmentally programmed sex differences in the hippocampal structure that mat help explain why male and female rats use different strategies to solve spatial navigation problems. During the period of development when testosterone is elevated in the male, aromatase and estrogen receptors are transiently expressed in the hippocampus. Recent data on behavior and synapse induction strongly suggest that this pathway is involved in the masculinization or defeminization of hippocampal structure and function. Third, ovarian steroids have effects throughout the brain, including effects on brainstem and midbrain catecholaminergic neurons, midbrain serotonergic pathways, and the basal forebrain cholinergic system. Regulation of the serotonergic system appears to be linked to the presence of estrogen- and progestin-sensitive neurons in the midbrain raphe, whereas the ovarian steroid influence on cholinergic function involves induction of choline acetyltransferase and acetylcholinesterase according to a sexually dimorphic pattern. Because of these widespread influences on these various neuronal systems, it is not surprising that ovarian steroids produce measurable cognitive effects after ovariectomy and during aging.
卵巢甾体激素在整个生命周期中对大脑有诸多影响,始于妊娠期并持续至衰老期。这些激素会影响大脑中并非主要参与生殖的区域,如基底前脑、海马体、尾状壳核、中脑缝际核和脑干蓝斑核。在此,我们讨论雌激素和孕激素的三种与记忆过程特别相关的作用,并确定与衰老和神经退行性疾病相关的激素变化。首先,在雌性大鼠4至5天的发情周期中,雌激素和孕激素会调节海马体CA1区的突触形成。雌二醇可诱导新的兴奋性突触形成,且涉及N-甲基-D-天冬氨酸(NMDA)受体,而突触下调则涉及细胞内孕激素受体。其次,海马体结构存在发育编程性的性别差异,这有助于解释为何雄性和雌性大鼠解决空间导航问题时采用不同策略。在雄性大鼠睾酮水平升高的发育阶段,海马体中会短暂表达芳香化酶和雌激素受体。近期关于行为和突触诱导的数据有力地表明,该途径参与了海马体结构和功能的雄性化或去雌性化过程。第三,卵巢甾体激素对整个大脑都有影响,包括对脑干和中脑儿茶酚胺能神经元、中脑5-羟色胺能通路以及基底前脑胆碱能系统的影响。5-羟色胺能系统的调节似乎与中脑缝际核中雌激素和孕激素敏感神经元的存在有关,而卵巢甾体激素对胆碱能功能的影响则涉及根据性别二态性模式诱导胆碱乙酰转移酶和乙酰胆碱酯酶。由于对这些不同神经元系统有广泛影响,卵巢甾体激素在卵巢切除术后和衰老过程中产生可测量的认知影响也就不足为奇了。