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In vivo functional neurochemistry of human cortical cholinergic function during visuospatial attention

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In vivo functional neurochemistry of human cortical cholinergic function during visuospatial attention. / Lindner, Michael; Bell, Tiffany; Iqbal, Somya et al.
In: PLoS ONE, Vol. 12, No. 2, e0171338, 13.02.2017.

Research output: Contribution to journal › Article › peer-review

HarvardHarvard

Lindner, M, Bell, T, Iqbal, S, Mullins, PG & Christakou, A 2017, 'In vivo functional neurochemistry of human cortical cholinergic function during visuospatial attention', PLoS ONE, vol. 12, no. 2, e0171338. https://doi.org/10.1371/journal.pone.0171338

APA

Lindner, M., Bell, T., Iqbal, S., Mullins, P. G., & Christakou, A. (2017). In vivo functional neurochemistry of human cortical cholinergic function during visuospatial attention. PLoS ONE, 12(2), Article e0171338. https://doi.org/10.1371/journal.pone.0171338

CBE

Lindner M, Bell T, Iqbal S, Mullins PG, Christakou A. 2017. In vivo functional neurochemistry of human cortical cholinergic function during visuospatial attention. PLoS ONE. 12(2):Article e0171338. https://doi.org/10.1371/journal.pone.0171338

MLA

Lindner, Michael et al. "In vivo functional neurochemistry of human cortical cholinergic function during visuospatial attention". PLoS ONE. 2017. 12(2). https://doi.org/10.1371/journal.pone.0171338

VancouverVancouver

Lindner M, Bell T, Iqbal S, Mullins PG, Christakou A. In vivo functional neurochemistry of human cortical cholinergic function during visuospatial attention. PLoS ONE. 2017 Feb 13;12(2):e0171338. doi: 10.1371/journal.pone.0171338

Author

Lindner, Michael ; Bell, Tiffany ; Iqbal, Somya et al. / In vivo functional neurochemistry of human cortical cholinergic function during visuospatial attention. In: PLoS ONE. 2017 ; Vol. 12, No. 2.

RIS

TY - JOUR

T1 - In vivo functional neurochemistry of human cortical cholinergic function during visuospatial attention

AU - Lindner, Michael

AU - Bell, Tiffany

AU - Iqbal, Somya

AU - Mullins, Paul Gerald

AU - Christakou, Anastasia

N1 - The study was supported by a Human Frontier Science Program (www.hfsp.org) grant to AC (RGP0048/2012)

PY - 2017/2/13

Y1 - 2017/2/13

N2 - Cortical acetylcholine is involved in key cognitive processes such as visuospatial attention. Dysfunction in the cholinergic system has been described in a number of neuropsychiatric disorders. Levels of brain acetylcholine can be pharmacologically manipulated, but it is not possible to directly measure it in vivo in humans. However, key parts of its biochemical cascade in neural tissue, such as choline, can be measured using magnetic resonance spectroscopy (MRS). There is evidence that levels of choline may be an indirect but proportional measure of acetylcholine availability in brain tissue. In this study, we measured relative choline levels in the parietal cortex using functional (event-related) MRS (fMRS) during performance of a visuospatial attention task, with a modelling approach verified using simulated data. We describe a task-driven interaction effect on choline concentration, specifically driven by contralateral attention shifts. Our results suggest that choline MRS has the potential to serve as a proxy of brain acetylcholine function in humans.

AB - Cortical acetylcholine is involved in key cognitive processes such as visuospatial attention. Dysfunction in the cholinergic system has been described in a number of neuropsychiatric disorders. Levels of brain acetylcholine can be pharmacologically manipulated, but it is not possible to directly measure it in vivo in humans. However, key parts of its biochemical cascade in neural tissue, such as choline, can be measured using magnetic resonance spectroscopy (MRS). There is evidence that levels of choline may be an indirect but proportional measure of acetylcholine availability in brain tissue. In this study, we measured relative choline levels in the parietal cortex using functional (event-related) MRS (fMRS) during performance of a visuospatial attention task, with a modelling approach verified using simulated data. We describe a task-driven interaction effect on choline concentration, specifically driven by contralateral attention shifts. Our results suggest that choline MRS has the potential to serve as a proxy of brain acetylcholine function in humans.

U2 - 10.1371/journal.pone.0171338

DO - 10.1371/journal.pone.0171338

M3 - Article

C2 - 28192451

VL - 12

JO - PLoS ONE

JF - PLoS ONE

SN - 1932-6203

IS - 2

M1 - e0171338

ER -