Lab for Molecular Neuroscience, Clinic for Mental Health, University Hospital Muenster, 48149 Muenster, Germany.
Int J Mol Sci. 2021 Feb 2;22(3):1485. doi: 10.3390/ijms22031485.
Distinct from ovarian estradiol, the steroid hormone 17ß-estradiol (E2) is produced in the brain and is involved in numerous functions, particularly acting as a neurosteroid. However, the physiological role of E2 and the mechanism of its effects are not well known. In hippocampal slices, 17ß-estradiol has been found to cause a modest increase in fast glutamatergic transmission; because some of these effects are rapid and acute, they might be mediated by membrane-associated receptors via nongenomic action. Moreover, activation of membrane estrogen receptors can rapidly modulate neuron function in a sex-specific manner. To further investigate the neurological role of E2, we examined the effect of E2, as an estrogen receptor (ER) agonist, on synaptic transmission in slices of the prefrontal cortex (PFC) and hippocampus in both male and female mice. Whole-cell recordings of spontaneous excitatory postsynaptic currents (sEPSC) in the PFC showed that E2 acts as a neuromodulator in glutamatergic transmission in the PFC in both sexes, but often in a cell-specific manner. The sEPSC amplitude and/or frequency responded to E2 in three ways, namely by significantly increasing, decreasing or having no response. Additional experiments using an agonist selective for ERß, diarylpropionitrile (DPN) showed that in males the sEPSC and spontaneous inhibitory postsynaptic currents sIPSC responses were similar to their E2 responses, but in females the estrogen receptor ß (ERß) agonist DPN did not influence excitatory transmission in the PFC. In contrast, in the hippocampus of both sexes E2 potentiated the gluatmatergic synaptic transmission in a subset of hippocampal cells. These data indicate that activation of E2 targeting probably a estrogen subtypes or different downstream signaling affect synaptic transmission in the brain PFC and hippocampus between males versus females mice.
与卵巢雌二醇不同,甾体激素 17β-雌二醇(E2)在大脑中产生,参与许多功能,特别是作为神经甾体。然而,E2 的生理作用及其作用机制尚不清楚。在海马切片中,发现 17β-雌二醇可引起快速谷氨酸能传递适度增加;由于其中一些效应是快速和急性的,它们可能通过膜相关受体通过非基因组作用介导。此外,膜雌激素受体的激活可以快速调节神经元功能以性别特异性方式。为了进一步研究 E2 的神经作用,我们研究了 E2(作为雌激素受体(ER)激动剂)对雄性和雌性小鼠前额叶皮层(PFC)和海马切片中突触传递的影响。PFC 中的自发兴奋性突触后电流(sEPSC)的全细胞膜记录表明,E2 作为一种神经调节剂在 PFC 中的谷氨酸能传递中发挥作用,但通常以细胞特异性方式发挥作用。sEPSC 幅度和/或频率以三种方式对 E2 做出反应,即通过显著增加、减少或无反应。使用选择性 ERβ激动剂二芳基丙腈(DPN)进行的额外实验表明,在雄性中,sEPSC 和自发抑制性突触后电流 sIPSC 反应与 E2 反应相似,但在雌性中,雌激素受体β(ERβ)激动剂 DPN 不会影响 PFC 中的兴奋性传递。相比之下,在两性的海马中,E2 增强了谷氨酸能突触传递在海马细胞的亚群中。这些数据表明,激活 E2 靶向可能是雌激素亚型或不同的下游信号转导影响雄性与雌性小鼠大脑 PFC 和海马中的突触传递。