Effects of systemic clonidine on auditory event-related potentials in squirrel monkeys
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Cited by (51)
Neural responses to sensory novelty with and without conscious access
2022, NeuroImageCitation Excerpt :Similar to the phasic pupil response, the P3 has also been proposed to partially reflect NE-mediated adaptation of arousal and attentional reorientation (Aston-Jones and Cohen, 2005; Masson and Bidet-Caulet, 2019; Nieuwenhuis et al., 2005, 2011). This idea is confirmed by pharmacological and lesion studies in non-human primates which have shown how the LC-NE system causally contributes to the amplitude of the P3 response (Pineda et al., 1989; Swick et al., 1994). Hence, we suggest that this positive relationship reflects the shared neural substrates of the orienting-attention component of the pupil response and of the novelty P3 (Liao et al., 2016; Nieuwenhuis et al., 2005; Polich, 2007; Ranganath and Rainer, 2003).
Auditory event-related potentials in separating patients with depressive disorders and non-depressed controls: A narrative review
2022, International Journal of PsychophysiologyCitation Excerpt :Thus, ERP components can be used as tools to examine the differences in the specific information processing stages between MDD patients and non-depressed control participants, contributing to a better understanding of the neurophysiological underpinnings of the cognitive dysfunctions in MDD. Furthermore, ERPs are modulated by neurotransmitters, such as serotonin, dopamine, noradrenaline and glutamate (e.g., Hegerl and Juckel, 1993; Liu et al., 2009; Pogarell et al., 2011; Swick et al., 1994; Umbricht et al., 2000), that have been implicated in the pathophysiology of depression (e.g., Belujon and Grace, 2017; Malhi et al., 2005; Moret and Briley, 2011; Moriguchi et al., 2019). In this narrative review, we bring together findings about whether there are deficits in patients with MDD in the early pre-attentive cognitive processing stage reflecting automatic change detection (MMN) and the later attentive cognitive processing stage reflecting attentional and working memory operations (P3).
Short- and long-lasting consequences of novelty, deviance and surprise on brain and cognition
2015, Neuroscience and Biobehavioral ReviewsCitation Excerpt :The P3 has been shown to depend on NE in several ways. For example, a P3-like response in monkeys was fully attenuated when the LC was lesioned (Pineda et al., 1989), and by a psychopharmacological intervention that depletes NE (Swick et al., 1994a,b). In turn, novelty can drive LC phasic activity.
Genetic marker of norepinephrine synthesis predicts individual differences in post-error slowing: A pilot study
2013, NeuropsychologiaCitation Excerpt :Informative scalp-EEG measures include the P300 (Nunez Castellar et al., 2010) and EEG alpha power, two cortical correlates of the orienting response and increased LC–NE activity (Nieuwenhuis et al., 2011; Swick et al., 1994; Swick et al., 1994).
Dexamphetamine reduces auditory P3 delta power and phase-locking while increasing gamma power
2012, European NeuropsychopharmacologyCitation Excerpt :In contrast to the above with dopaminergic drugs, the region of the noradrenergic cell bodies that projects to forebrain areas via the dorsal noradrenergic bundle, the locus coeruleus (LC), has been implicated as a generator of the P3 (Nieuwenhuis et al., 2005). Pharmacological support comes from clonidine-induced P3 reductions in humans (Halliday et al., 1994) and monkeys (Swick et al., 1994), but not always consistently (Shelley et al., 1997). However, clonidine is an adrenergic alpha2 auto-receptor agonist, and the action of clonidine is to inhibit both noradrenaline and dopamine release (Murai et al., 1998), yielding an action that is functionally opposite to the effect of dexamphetamine.
Noradrenaline involvement in basic and higher integrated REM sleep processes
2008, Progress in Neurobiology