Davis School of Gerontology,University of Southern California,Los Angeles,CA
Neuroscience Graduate Program,University of Southern California,Los Angeles,CA
Behav Brain Sci. 2016 Jan;39:e200. doi: 10.1017/S0140525X15000667. Epub 2015 Jul 1.
Emotional arousal enhances perception and memory of high-priority information but impairs processing of other information. Here, we propose that, under arousal, local glutamate levels signal the current strength of a representation and interact with norepinephrine (NE) to enhance high priority representations and out-compete or suppress lower priority representations. In our "glutamate amplifies noradrenergic effects" (GANE) model, high glutamate at the site of prioritized representations increases local NE release from the locus coeruleus (LC) to generate "NE hotspots." At these NE hotspots, local glutamate and NE release are mutually enhancing and amplify activation of prioritized representations. In contrast, arousal-induced LC activity inhibits less active representations via two mechanisms: 1) Where there are hotspots, lateral inhibition is amplified; 2) Where no hotspots emerge, NE levels are only high enough to activate low-threshold inhibitory adrenoreceptors. Thus, LC activation promotes a few hotspots of excitation in the context of widespread suppression, enhancing high priority representations while suppressing the rest. Hotspots also help synchronize oscillations across neural ensembles transmitting high-priority information. Furthermore, brain structures that detect stimulus priority interact with phasic NE release to preferentially route such information through large-scale functional brain networks. A surge of NE before, during, or after encoding enhances synaptic plasticity at NE hotspots, triggering local protein synthesis processes that enhance selective memory consolidation. Together, these noradrenergic mechanisms promote selective attention and memory under arousal. GANE not only reconciles apparently contradictory findings in the emotion-cognition literature but also extends previous influential theories of LC neuromodulation by proposing specific mechanisms for how LC-NE activity increases neural gain.
情绪唤醒增强了对高优先级信息的感知和记忆,但会损害对其他信息的处理。在这里,我们提出在唤醒状态下,局部谷氨酸水平信号表示当前的强度,并与去甲肾上腺素(NE)相互作用,以增强高优先级表示,并竞争或抑制低优先级表示。在我们的“谷氨酸增强去甲肾上腺素能效应”(GANE)模型中,高优先级表示部位的高谷氨酸会增加蓝斑核(LC)从中释放的局部去甲肾上腺素,从而产生“NE 热点”。在这些 NE 热点处,局部谷氨酸和去甲肾上腺素的释放相互增强,并放大了高优先级表示的激活。相比之下,唤醒引起的 LC 活动通过两种机制抑制不活跃的表示:1)在存在热点的地方,侧向抑制被放大;2)在没有热点出现的地方,去甲肾上腺素水平仅高到足以激活低阈值抑制性肾上腺素受体。因此,LC 激活在广泛抑制的背景下促进了少数兴奋热点的出现,增强了高优先级的表示,同时抑制了其余的表示。热点还有助于在传递高优先级信息的神经集合中同步振荡。此外,检测刺激优先级的大脑结构与阵发性去甲肾上腺素释放相互作用,优先将此类信息通过大规模功能大脑网络传递。在编码之前、期间或之后的 NE 激增增强了 NE 热点处的突触可塑性,触发了局部蛋白质合成过程,从而增强了选择性记忆巩固。总之,这些去甲肾上腺素能机制在唤醒状态下促进了选择性注意和记忆。GANE 不仅调和了情绪认知文献中明显矛盾的发现,而且通过提出 LC-NE 活动如何增加神经增益的具体机制,扩展了先前关于 LC 神经调节的有影响力的理论。