Maggi A, Perez J
Life Sci. 1985 Sep 9;37(10):893-906. doi: 10.1016/0024-3205(85)90525-9.
The large body of evidence presented indicates that in the brain the action of sex hormones cannot be thought as restricted to the regulation of endocrine functions and mating behavior. Estrogens and progesterone seem to act in numerous regions of the CNS to regulate motor as well as limbic functions. Furthermore, the data reviewed indicate that these hormones may modulate neuronal activity through a wide variety of mechanisms. More studies should focus on such mechanisms in order to better understand the role of sex hormones in the CNS and to devise ways of limiting their effects on depression, epilepsy etc. It is known that in peripheral target organs these hormones modulate cell activities by binding to specific receptors which can recognize the DNA sequence and activate the transcription of selected genes (135, 136). There is evidence supporting the hypothesis that this mechanism of action has been conserved also in the brain. First, the brain receptors for progesterone and estrogens are functionally and biochemically indistinguishable from those in the periphery (4, 5): they may be concentrated in neuronal nuclei and bind chromatin "in vitro" (7). Second, a temporal relationship has been observed between administration of steroids and the increase of polymerase II activity (137) and protein synthesis (4, 5). Third, various hormone-induced behaviors may be blocked by inhibitors of the protein synthesis (138, 139, 140, 141). However, sex hormones must be capable to regulate neuronal functions by mechanisms other then genomic. In fact, the topical application of estrogen or progesterone on nervous tissue results in a rapid change of membrane potential (60, 71). Such a rapid effect is not likely to be the consequence of nuclear action, but rather must be related to events occurring on the cell surface. It has been hypothesized that sex steroids affect the fluidity of the cell membrane, therefore modifying the ion transport or neurotransmitter receptor activity (142). If this were the case we would expect to observe a similar effect after application of any steroid. Experimental evidence demonstrates that not all the steroids affect the nervous membrane potential. Moreover, two steroids, estradiol and progesterone, have been described to modulate membrane potential in an opposite way (66, 67, 69, 75). At the moment, there is no evidence for the presence of steroid receptors on neuronal membranes which could mediate the described phenomena.(ABSTRACT TRUNCATED AT 400 WORDS)
所呈现的大量证据表明,在大脑中,性激素的作用不能被认为仅限于调节内分泌功能和交配行为。雌激素和孕酮似乎在中枢神经系统的许多区域发挥作用,以调节运动功能和边缘系统功能。此外,所综述的数据表明,这些激素可能通过多种机制调节神经元活动。更多的研究应聚焦于这些机制,以便更好地理解性激素在中枢神经系统中的作用,并设计出限制其对抑郁症、癫痫等影响的方法。众所周知,在周围靶器官中,这些激素通过与特定受体结合来调节细胞活动,这些受体能够识别DNA序列并激活所选基因的转录(135, 136)。有证据支持这样的假说,即这种作用机制在大脑中也得以保留。首先,孕酮和雌激素的脑受体在功能和生化方面与外周受体并无区别(4, 5):它们可能集中在神经元细胞核中,并在“体外”与染色质结合(7)。其次,已观察到类固醇给药与聚合酶II活性(137)和蛋白质合成(4, 5)增加之间存在时间关系。第三,各种激素诱导的行为可能会被蛋白质合成抑制剂阻断(138, 139, 140, 141)。然而,性激素必须能够通过基因组以外的机制调节神经元功能。事实上,将雌激素或孕酮局部应用于神经组织会导致膜电位迅速变化(60, 71)。这种快速效应不太可能是核作用的结果,而必定与细胞表面发生的事件有关。据推测,性类固醇会影响细胞膜的流动性,从而改变离子转运或神经递质受体活性(142)。如果是这样的话,我们预计在应用任何类固醇后都会观察到类似的效果。实验证据表明,并非所有类固醇都会影响神经膜电位。此外,已描述两种类固醇,雌二醇和孕酮,以相反的方式调节膜电位(66, 67, 69, 75)。目前,没有证据表明神经元膜上存在能够介导上述现象的类固醇受体。(摘要截断于400字)