2012
DOI: 10.1038/srep00417
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Noradrenergic ‘Tone’ Determines Dichotomous Control of Cortical Spike-Timing-Dependent Plasticity

Abstract: Norepinephrine (NE) is widely distributed throughout the brain. It modulates intrinsic currents, as well as amplitude and frequency of synaptic transmission affecting the ‘signal-to-noise ratio’ of sensory responses. In the visual cortex, α1- and β-adrenergic receptors (AR) gate opposing effects on long-term plasticity of excitatory transmission. Whether and how NE recruits these plastic mechanisms is not clear. Here, we show that NE modulates glutamatergic inputs with different efficacies for α1- and β-AR. As… Show more

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Cited by 71 publications
(71 citation statements)
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References 27 publications
(54 reference statements)
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“…The differences in learning rate and side bias between the SSIM dec,wide and SSIM inc,wide groups, suggest that attention signals and/or diffuse neuromodulatory systems were differentially engaged in these groups94647. It has been reported that attention functions as a gate to ensure that visual perceptual learning occurs only in response to features to which attention is directed (task-relevant features), enhancing the stream of signals to specific brain areas24.…”
Section: Discussionmentioning
confidence: 99%
“…The differences in learning rate and side bias between the SSIM dec,wide and SSIM inc,wide groups, suggest that attention signals and/or diffuse neuromodulatory systems were differentially engaged in these groups94647. It has been reported that attention functions as a gate to ensure that visual perceptual learning occurs only in response to features to which attention is directed (task-relevant features), enhancing the stream of signals to specific brain areas24.…”
Section: Discussionmentioning
confidence: 99%
“…The LC is a small bilateral nucleus located in the dorsal pontine tegmentum (PT) and is the primary source of NE for the brain. Via its widespread release under arousal, NE enhances learning (Ahissar et al, 1996; Chamberlain et al, 2006; Harley, 1987), regulates synaptic plasticity (Ahissar et al, 1996; Neuman and Harley, 1983; Salgado et al, 2012), and optimizes high-order cognitive processes, including working memory (Arnsten and Li, 2005; Wang et al, 2007). NE is also neuroprotective and can lower toxicity in neurons (Counts and Mufson, 2010) and buffer neurons from oxidative stress (Troadec et al, 2001).…”
Section: Introductionmentioning
confidence: 99%
“…According to GANE, NE released under arousal modulates mental representations differently as a function of their activation strength, such that NE enhances prioritized inputs even further, while simultaneously suppressing noisy or weak inputs. This selective up-regulation of salient representations is achieved via positive local glutamate-NE feedback loops that generate sufficiently elevated levels of local NE to engage low-affinity β-adrenoreceptors; in turn, β-adrenoreceptor activation potentiates pre- and postsynaptic excitatory activity (Berridge & Waterhouse, 2003) and triggers synaptic plasticity processes that support memory consolidation (Marzo et al, 2009; Salgado et al, 2012; Treviño et al, 2012). At the same time, high glutamatergic activity representing strong inputs should also stimulate local GABAergic activity that inhibits weaker, competing representations (Brown et al, 2005).…”
Section: Introductionmentioning
confidence: 99%