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Cholinergic modulation of cognition: Insights from human pharmacological functional neuroimaging
Evidence from lesion and cortical-slice studies implicate the neocortical cholinergic system in the modulation of sensory, attentional and memory processing. In this review we consider findings from sixty-three healthy human cholinergic functional neuroimaging studies that probe interactions of chol...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Pergamon Press
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3382716/ https://www.ncbi.nlm.nih.gov/pubmed/21708219 http://dx.doi.org/10.1016/j.pneurobio.2011.06.002 |
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author | Bentley, Paul Driver, Jon Dolan, Raymond J. |
author_facet | Bentley, Paul Driver, Jon Dolan, Raymond J. |
author_sort | Bentley, Paul |
collection | PubMed |
description | Evidence from lesion and cortical-slice studies implicate the neocortical cholinergic system in the modulation of sensory, attentional and memory processing. In this review we consider findings from sixty-three healthy human cholinergic functional neuroimaging studies that probe interactions of cholinergic drugs with brain activation profiles, and relate these to contemporary neurobiological models. Consistent patterns that emerge are: (1) the direction of cholinergic modulation of sensory cortex activations depends upon top-down influences; (2) cholinergic hyperstimulation reduces top-down selective modulation of sensory cortices; (3) cholinergic hyperstimulation interacts with task-specific frontoparietal activations according to one of several patterns, including: suppression of parietal-mediated reorienting; decreasing ‘effort’-associated activations in prefrontal regions; and deactivation of a ‘resting-state network’ in medial cortex, with reciprocal recruitment of dorsolateral frontoparietal regions during performance-challenging conditions; (4) encoding-related activations in both neocortical and hippocampal regions are disrupted by cholinergic blockade, or enhanced with cholinergic stimulation, while the opposite profile is observed during retrieval; (5) many examples exist of an ‘inverted-U shaped’ pattern of cholinergic influences by which the direction of functional neural activation (and performance) depends upon both task (e.g. relative difficulty) and subject (e.g. age) factors. Overall, human cholinergic functional neuroimaging studies both corroborate and extend physiological accounts of cholinergic function arising from other experimental contexts, while providing mechanistic insights into cholinergic-acting drugs and their potential clinical applications. |
format | Online Article Text |
id | pubmed-3382716 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Pergamon Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-33827162012-07-05 Cholinergic modulation of cognition: Insights from human pharmacological functional neuroimaging Bentley, Paul Driver, Jon Dolan, Raymond J. Prog Neurobiol Article Evidence from lesion and cortical-slice studies implicate the neocortical cholinergic system in the modulation of sensory, attentional and memory processing. In this review we consider findings from sixty-three healthy human cholinergic functional neuroimaging studies that probe interactions of cholinergic drugs with brain activation profiles, and relate these to contemporary neurobiological models. Consistent patterns that emerge are: (1) the direction of cholinergic modulation of sensory cortex activations depends upon top-down influences; (2) cholinergic hyperstimulation reduces top-down selective modulation of sensory cortices; (3) cholinergic hyperstimulation interacts with task-specific frontoparietal activations according to one of several patterns, including: suppression of parietal-mediated reorienting; decreasing ‘effort’-associated activations in prefrontal regions; and deactivation of a ‘resting-state network’ in medial cortex, with reciprocal recruitment of dorsolateral frontoparietal regions during performance-challenging conditions; (4) encoding-related activations in both neocortical and hippocampal regions are disrupted by cholinergic blockade, or enhanced with cholinergic stimulation, while the opposite profile is observed during retrieval; (5) many examples exist of an ‘inverted-U shaped’ pattern of cholinergic influences by which the direction of functional neural activation (and performance) depends upon both task (e.g. relative difficulty) and subject (e.g. age) factors. Overall, human cholinergic functional neuroimaging studies both corroborate and extend physiological accounts of cholinergic function arising from other experimental contexts, while providing mechanistic insights into cholinergic-acting drugs and their potential clinical applications. Pergamon Press 2011-09-01 /pmc/articles/PMC3382716/ /pubmed/21708219 http://dx.doi.org/10.1016/j.pneurobio.2011.06.002 Text en © 2011 Elsevier Ltd. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license |
spellingShingle | Article Bentley, Paul Driver, Jon Dolan, Raymond J. Cholinergic modulation of cognition: Insights from human pharmacological functional neuroimaging |
title | Cholinergic modulation of cognition: Insights from human pharmacological functional neuroimaging |
title_full | Cholinergic modulation of cognition: Insights from human pharmacological functional neuroimaging |
title_fullStr | Cholinergic modulation of cognition: Insights from human pharmacological functional neuroimaging |
title_full_unstemmed | Cholinergic modulation of cognition: Insights from human pharmacological functional neuroimaging |
title_short | Cholinergic modulation of cognition: Insights from human pharmacological functional neuroimaging |
title_sort | cholinergic modulation of cognition: insights from human pharmacological functional neuroimaging |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3382716/ https://www.ncbi.nlm.nih.gov/pubmed/21708219 http://dx.doi.org/10.1016/j.pneurobio.2011.06.002 |
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