2018
DOI: 10.3389/fncir.2018.00051
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Monoaminergic Neuromodulation of Sensory Processing

Abstract: All neuronal circuits are subject to neuromodulation. Modulatory effects on neuronal processing and resulting behavioral changes are most commonly reported for higher order cognitive brain functions. Comparatively little is known about how neuromodulators shape processing in sensory brain areas that provide the signals for downstream regions to operate on. In this article, we review the current knowledge about how the monoamine neuromodulators serotonin, dopamine and noradrenaline influence the representation … Show more

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Cited by 113 publications
(105 citation statements)
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References 183 publications
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“…The prevailing interpretation emerging from these studies is that neuromodulators gate cortical plasticity by enhancing sensory perception, and by promoting patterns of cortical activity suitable for plasticity induction via controlling network excitability. This is consistent with a wealth of studies documenting that neuromodulators improve perception in vivo (see Gelbard-Sagiv et al, 2018;Jacob and Nienborg, 2018;McBurney-Lin et al, 2019;Nadim and Bucher, 2014 for reviews) also affect cellular intrinsic excitability and synaptic inhibition to gate the induction of Hebbian plasticity in vitro (see Brzosko et al, 2019;Palacios-Filardo and Mellor, 2019;Pawlak et al, 2010 for reviews). We propose an additional and different mode of action: direct control of the expression, not the induction, of Hebbian plasticity via the Gq/Gs based pull-push metaplasticity mechanism that we previously demonstrated in vitro, in slices.…”
Section: Discussionsupporting
confidence: 79%
“…The prevailing interpretation emerging from these studies is that neuromodulators gate cortical plasticity by enhancing sensory perception, and by promoting patterns of cortical activity suitable for plasticity induction via controlling network excitability. This is consistent with a wealth of studies documenting that neuromodulators improve perception in vivo (see Gelbard-Sagiv et al, 2018;Jacob and Nienborg, 2018;McBurney-Lin et al, 2019;Nadim and Bucher, 2014 for reviews) also affect cellular intrinsic excitability and synaptic inhibition to gate the induction of Hebbian plasticity in vitro (see Brzosko et al, 2019;Palacios-Filardo and Mellor, 2019;Pawlak et al, 2010 for reviews). We propose an additional and different mode of action: direct control of the expression, not the induction, of Hebbian plasticity via the Gq/Gs based pull-push metaplasticity mechanism that we previously demonstrated in vitro, in slices.…”
Section: Discussionsupporting
confidence: 79%
“…Due to the heterogeneity of involved processing steps, the identification of putative neuronal correlates of age-related changes is rather complex. Essentially all cortical areas are subject to substantial volume decline during aging (Raz et al, 2004), but changes in connectivity and compromised neuromodulation might be most relevant for complex perceptual decline (Damoiseaux, 2017;Jacob & Nienborg, 2018).…”
Section: Age-related Changes In High-level Processingmentioning
confidence: 99%
“…OTR knockdown increased the number of perineuronal nets in the S1 (Figs 4I-K), while it decreased the number of perineuronal nets in the lOFC (Fig 4Q). These effects of OTR knockdown may have been driven by serotonin’s potentiation of cortical inhibition 68,78 , with serotonin release associated with decreased activity of the S1 in response to tactile stimulation in both female rats 79,80 and women 68 . Perineuronal nets are generated in response to neural activity 73 , so greater S1 activity and lower lOFC activity could have led to the higher and lower number of perineuronal nets in the S1 and lOFC, respectively (Figs 4I-K, 4Q).…”
Section: Otrs Influence Cortical Serotonin and Perineuronal Netsmentioning
confidence: 99%