Evidence map›Paper›PMID 38617349›Full record

ArticlebioRxiv : the preprint server for biology2024

Orbitofrontal high-gamma reflects spike-dissociable value and decision mechanisms.

Dixit Sharma, Shira M Lupkin, Vincent B McGinty

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In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Dixit SharmaCenter for Molecular and Behavioral Neuroscience, Rutgers University - Newark.ORCID 0000-0003-2024-5892
Shira M LupkinCenter for Molecular and Behavioral Neuroscience, Rutgers University - Newark.ORCID 0000-0002-3792-5571
Vincent B McGintyCenter for Molecular and Behavioral Neuroscience, Rutgers University - Newark.ORCID 0000-0003-0883-4301

Funding

Cellular Mechanisms of Gaze-Biased Choice PreferenceK01DA036659 · NIDA · STANFORD UNIVERSITY · PI MCGINTY, VINCENT B · 2014 to 2018
$831k
NIDA NIH HHS K01 DA036659
6 · The paper itself

Abstract

The orbitofrontal cortex (OFC) plays a crucial role in value-based decision-making. While previous research has focused on spiking activity in OFC neurons, the role of OFC local field potentials (LFPs) in decision-making remains unclear. LFPs are important because they can reflect synaptic and subthreshold activity not directly coupled to spiking, and because they are potential targets for less invasive forms of brain-machine interface (BMI). We recorded LFPs and spiking activity using multi-channel vertical probes while monkeys performed a two-option value-based decision-making task. We compared the value- and decision-coding properties of high-gamma range LFPs (HG, 50-150 Hz) to the coding properties of spiking multi-unit activity (MUA) recorded concurrently on the same electrodes. Results show that HG and MUA both represent the values of decision targets, and that their representations have similar temporal profiles in a trial. However, we also identified value-coding properties of HG that were dissociable from the concurrently-measured MUA. On average across channels, HG amplitude increased monotonically with value, whereas the average value encoding in MUA was net neutral. HG also encoded a signal consistent with a comparison between the values of the two targets, a signal which was much weaker in MUA. In individual channels, HG was better able to predict choice outcomes than MUA; however, when simultaneously recorded channels were combined in population-based decoder, MUA provided more accurate predictions than HG. Interestingly, HG value representations were accentuated in channels in or near shallow cortical layers, suggesting a dissociation between neuronal sources of HG and MUA. In summary, we find that HG signals are dissociable from MUA with respect to cognitive variables encoded in prefrontal cortex, evident in the monotonic encoding of value, stronger encoding of value comparisons, and more accurate predictions about behavior. High-frequency LFPs may therefore be a viable - or even preferable - target for BMIs to assist cognitive function, opening the possibility for less invasive access to mental contents that would otherwise be observable only with spike-based measures.

Identifiers

PMID38617349
PMCPMC11014579

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.