Department of Neuroscience & Centre for the Cellular Basis of Behaviour, 125 Coldharbour Lane, The James Black Centre, Institute of Psychiatry, King's College London, London, SE5 9NU, UK.
Pharmacol Rev. 2013 Sep 27;65(4):1318-50. doi: 10.1124/pr.111.005272. Print 2013.
Converging evidence from cellular, electrophysiological, anatomic, and behavioral studies suggests that the remodeling of synapse structure and function is a critical component of cognition. This modulation of neuroplasticity can be achieved through the actions of numerous extracellular signals. Moreover, it is thought that it is the integration of different extracellular signals regulation of neuroplasticity that greatly influences cognitive function. One group of signals that exerts powerful effects on multiple neurologic processes is estrogens. Classically, estrogens have been described to exert their effects over a period of hours to days. However, there is now increasing evidence that estrogens can rapidly influence multiple behaviors, including those that require forebrain neural circuitry. Moreover, these effects are found in both sexes. Critically, it is now emerging that the modulation of cognition by rapid estrogenic signaling is achieved by activation of specific signaling cascades and regulation of synapse structure and function, cumulating in the rewiring of neural circuits. The importance of understanding the rapid effects of estrogens on forebrain function and circuitry is further emphasized as investigations continue to consider the potential of estrogenic-based therapies for neuropathologies. This review focuses on how estrogens can rapidly influence cognition and the emerging mechanisms that underlie these effects. We discuss the potential sources and the biosynthesis of estrogens within the brain and the consequences of rapid estrogenic-signaling on the remodeling of neural circuits. Furthermore, we argue that estrogens act via distinct signaling pathways to modulate synapse structure and function in a manner that may vary with cell type, developmental stage, and sex. Finally, we present a model in which the coordination of rapid estrogenic-signaling and activity-dependent stimuli can result in long-lasting changes in neural circuits, contributing to cognition, with potential relevance for the development of novel estrogenic-based therapies for neurodevelopmental or neurodegenerative disorders.
来自细胞、电生理学、解剖学和行为研究的综合证据表明,突触结构和功能的重塑是认知的关键组成部分。这种神经可塑性的调节可以通过许多细胞外信号的作用来实现。此外,人们认为,不同细胞外信号对神经可塑性的调节的整合极大地影响了认知功能。一组对多种神经过程产生强大影响的信号是雌激素。经典地,雌激素被描述为在数小时到数天的时间内发挥作用。然而,现在越来越多的证据表明,雌激素可以迅速影响多种行为,包括需要前脑神经回路的行为。此外,这些效应在两性中都有发现。关键的是,现在出现的情况是,雌激素通过快速信号转导对认知的调节是通过激活特定的信号级联和调节突触结构和功能来实现的,最终导致神经网络的重新布线。理解雌激素对前脑功能和回路的快速影响的重要性进一步强调了,因为研究继续考虑基于雌激素的疗法对神经病理学的潜在作用。这篇综述集中讨论了雌激素如何迅速影响认知以及这些效应背后的新兴机制。我们讨论了脑内雌激素的潜在来源和生物合成,以及快速雌激素信号对神经回路重塑的影响。此外,我们认为雌激素通过不同的信号通路作用于调节突触结构和功能,其方式可能因细胞类型、发育阶段和性别而异。最后,我们提出了一个模型,其中快速雌激素信号和活动依赖性刺激的协调可以导致神经网络的持久变化,从而对认知产生影响,这对于开发新型基于雌激素的治疗神经发育或神经退行性疾病的疗法具有潜在的意义。