Regional Striatal Cholinergic Involvement in Human Behavioral Flexibility

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Regional Striatal Cholinergic Involvement in Human Behavioral Flexibility. / Bell, Tiffany; Lindner, Michael; Langdon, Angela et al.
In: Journal of Neuroscience, Vol. 39, No. 29, 17.07.2019, p. 5740-5749.

Research output: Contribution to journalArticlepeer-review

HarvardHarvard

Bell, T, Lindner, M, Langdon, A, Mullins, PG & Christakou, A 2019, 'Regional Striatal Cholinergic Involvement in Human Behavioral Flexibility', Journal of Neuroscience, vol. 39, no. 29, pp. 5740-5749. https://doi.org/10.1523/JNEUROSCI.2110-18.2019

APA

Bell, T., Lindner, M., Langdon, A., Mullins, P. G., & Christakou, A. (2019). Regional Striatal Cholinergic Involvement in Human Behavioral Flexibility. Journal of Neuroscience, 39(29), 5740-5749. https://doi.org/10.1523/JNEUROSCI.2110-18.2019

CBE

Bell T, Lindner M, Langdon A, Mullins PG, Christakou A. 2019. Regional Striatal Cholinergic Involvement in Human Behavioral Flexibility. Journal of Neuroscience. 39(29):5740-5749. https://doi.org/10.1523/JNEUROSCI.2110-18.2019

MLA

VancouverVancouver

Bell T, Lindner M, Langdon A, Mullins PG, Christakou A. Regional Striatal Cholinergic Involvement in Human Behavioral Flexibility. Journal of Neuroscience. 2019 Jul 17;39(29):5740-5749. doi: 10.1523/JNEUROSCI.2110-18.2019

Author

Bell, Tiffany ; Lindner, Michael ; Langdon, Angela et al. / Regional Striatal Cholinergic Involvement in Human Behavioral Flexibility. In: Journal of Neuroscience. 2019 ; Vol. 39, No. 29. pp. 5740-5749.

RIS

TY - JOUR

T1 - Regional Striatal Cholinergic Involvement in Human Behavioral Flexibility

AU - Bell, Tiffany

AU - Lindner, Michael

AU - Langdon, Angela

AU - Mullins, Paul Gerald

AU - Christakou, Anastasia

N1 - This work was supported by Human Frontier Science Program GrantRGP0048/2012, and Engineering and Physical Sciences Research Council Doctoral Training Grant EP/L505043/1

PY - 2019/7/17

Y1 - 2019/7/17

N2 - Animal studies have shown that the striatal cholinergic system plays a role in behavioral flexibility but, until recently, this system could not be studied in humans due to a lack of appropriate noninvasive techniques. Using proton magnetic resonance spectroscopy, we recently showed that the concentration of dorsal striatal choline (an acetylcholine precursor) changes during reversal learning (a measure of behavioral flexibility) in humans. The aim of the present study was to examine whether regional average striatal choline was associated with reversal learning. A total of 22 participants (mean age = 25.2 years, range = 18-32 years, 13 female) reached learning criterion in a probabilistic learning task with a reversal component. We measured choline at rest in both the dorsal and ventral striatum using magnetic resonance spectroscopy. Task performance was described using a simple reinforcement learning model that dissociates the contributions of positive and negative prediction errors to learning. Average levels of choline in the dorsal striatum were associated with performance during reversal, but not during initial learning. Specifically, lower levels of choline in the dorsal striatum were associated with a lower number of perseverative trials. Moreover, choline levels explained interindividual variance in perseveration over and above that explained by learning from negative prediction errors. These findings suggest that the dorsal striatal cholinergic system plays an important role in behavioral flexibility, in line with evidence from the animal literature and our previous work in humans. Additionally, this work provides further support for the idea of measuring choline with magnetic resonance spectroscopy as a noninvasive way of studying human cholinergic neurochemistry.SIGNIFICANCE STATEMENT Behavioral flexibility is a crucial component of adaptation and survival. Evidence from the animal literature shows that the striatal cholinergic system is fundamental to reversal learning, a key paradigm for studying behavioral flexibility, but this system remains understudied in humans. Using proton magnetic resonance spectroscopy, we showed that choline levels at rest in the dorsal striatum are associated with performance specifically during reversal learning. These novel findings help to bridge the gap between animal and human studies by demonstrating the importance of cholinergic function in the dorsal striatum in human behavioral flexibility. Importantly, the methods described here cannot only be applied to furthering our understanding of healthy human neurochemistry, but also to extending our understanding of cholinergic disorders.

AB - Animal studies have shown that the striatal cholinergic system plays a role in behavioral flexibility but, until recently, this system could not be studied in humans due to a lack of appropriate noninvasive techniques. Using proton magnetic resonance spectroscopy, we recently showed that the concentration of dorsal striatal choline (an acetylcholine precursor) changes during reversal learning (a measure of behavioral flexibility) in humans. The aim of the present study was to examine whether regional average striatal choline was associated with reversal learning. A total of 22 participants (mean age = 25.2 years, range = 18-32 years, 13 female) reached learning criterion in a probabilistic learning task with a reversal component. We measured choline at rest in both the dorsal and ventral striatum using magnetic resonance spectroscopy. Task performance was described using a simple reinforcement learning model that dissociates the contributions of positive and negative prediction errors to learning. Average levels of choline in the dorsal striatum were associated with performance during reversal, but not during initial learning. Specifically, lower levels of choline in the dorsal striatum were associated with a lower number of perseverative trials. Moreover, choline levels explained interindividual variance in perseveration over and above that explained by learning from negative prediction errors. These findings suggest that the dorsal striatal cholinergic system plays an important role in behavioral flexibility, in line with evidence from the animal literature and our previous work in humans. Additionally, this work provides further support for the idea of measuring choline with magnetic resonance spectroscopy as a noninvasive way of studying human cholinergic neurochemistry.SIGNIFICANCE STATEMENT Behavioral flexibility is a crucial component of adaptation and survival. Evidence from the animal literature shows that the striatal cholinergic system is fundamental to reversal learning, a key paradigm for studying behavioral flexibility, but this system remains understudied in humans. Using proton magnetic resonance spectroscopy, we showed that choline levels at rest in the dorsal striatum are associated with performance specifically during reversal learning. These novel findings help to bridge the gap between animal and human studies by demonstrating the importance of cholinergic function in the dorsal striatum in human behavioral flexibility. Importantly, the methods described here cannot only be applied to furthering our understanding of healthy human neurochemistry, but also to extending our understanding of cholinergic disorders.

KW - Choline

KW - Cognitive flexibility

KW - Magnetic resonance spectroscopy

KW - Reversal Learning

KW - Striatum

U2 - 10.1523/JNEUROSCI.2110-18.2019

DO - 10.1523/JNEUROSCI.2110-18.2019

M3 - Article

C2 - 31109959

VL - 39

SP - 5740

EP - 5749

JO - Journal of Neuroscience

JF - Journal of Neuroscience

SN - 0270-6474

IS - 29

ER -