Norepinephrine ignites local hot spots of neuronal excitation: How arousal amplifies selectivity in perception and memory. (1st July 2015)

• Record Type: Journal Article
• Authors: Mather, Mara; Clewett, David; Sakaki, Michiko; Harley, Carolyn W.
• Is Part Of: Behavioral and brain sciences. Volume 38(2015)
• Page Start: 1
• Page End: 100
• Publication Date: 2015-07-01
• Subjects: arousal, -- attention, -- emotion, -- locus coeruleus, -- long-term consolidation, -- memory, -- norepinephrine, -- perception; Psychophysiology -- Periodicals; Psychology -- Periodicals; Human behavior -- Periodicals; Animal behavior -- Periodicals; Brain -- Periodicals; 616.89142
• DOI: 10.1017/S0140525X15000667
• Languages: English
• ISSNs: 0140-525X

Abstract

Abstract: Existing brain-based emotion-cognition theories fail to explain arousal's ability to both enhance and impair cognitive processing. In the Glutamate Amplifies Noradrenergic Effects (GANE) model outlined in this paper, we propose that arousal-induced norepinephrine (NE) released from the locus coeruleus (LC) biases perception and memory in favor of salient, high priority representations at the expense of lower priority representations. This increase in gain under phasic arousal occurs via synaptic self-regulation of NE based on glutamate levels. When the LC is phasically active, elevated levels of glutamate at the site of prioritized representations increase local NE release, creating "NE hot spots." At these local hot spots, glutamate and NE release are mutually enhancing and amplify activation of prioritized representations. This excitatory effect contrasts with widespread NE suppression of weaker representations via lateral and auto-inhibitory processes. On a broader scale, hot spots increase oscillatory synchronization across neural ensembles transmitting high priority information. Furthermore, key brain structures that detect or pre-determine 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 sites of high glutamate activity, triggering local protein synthesis processes that enhance selective memory consolidation. Together, these noradrenergic mechanisms increase perceptual and memory selectivity under arousal. Beyond explaining discrepancies in the emotion-cognition literature, GANE reconciles and extends previous influential theories of LC neuromodulation by highlighting how NE can produce such different outcomes in processing based on priority.