Evidence map›Paper›PMID 40767011›Full record

ArticleJournal of integrative neuroscience2025

Inactivation of Dorsolateral Prefrontal Cortex During Auditory Working Memory.

Bethany Plakke, Katryna Skye Kevelson, Charles Leyens, Lizabeth M Romanski

Abstract read
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Article in Journal of integrative neuroscience, 2025. 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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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Bethany PlakkeDepartment of Psychological Sciences, Kansas State University, Manhattan, KS 66502, USA.
Katryna Skye KevelsonDepartment of Neuroscience, University of Rochester School of Medicine, Rochester, NY 14642, USA.
Charles LeyensDepartment of Computer Science, Rochester Institute of Technology, Rochester, NY 14623, USA.
Lizabeth M RomanskiDepartment of Neuroscience, University of Rochester School of Medicine, Rochester, NY 14642, USA.

Funding

Auditory &Integrative Processes in Prefrontal CortexR01DC004845 · NIDCD · UNIVERSITY OF ROCHESTER · PI LIZABETH M ROMANSKI · 2001 to 2026
$9.5M
NIDCD NIH HHS R01 DC004845NIH/NIDCD DC04845University of Rochester GEBS Summer Scholar Award
6 · The paper itself

Abstract

backgroundThe dorsolateral prefrontal cortex (DLPFC) is a critical node in the working memory (WM) neural circuit, established through neurophysiology, neuropsychology, and neuroimaging studies in humans and nonhuman primates. While most of the neurophysiological evidence for the role of the DLPFC in WM comes from visuospatial WM paradigms, evidence for its role in auditory WM has been suggested by the fact that large lateral prefrontal cortex lesions in nonhuman primates cause auditory discrimination deficits. Moreover, DLPFC neurons demonstrate task-related neuronal responses during auditory WM. In contrast, other studies have proposed that the ventrolateral prefrontal cortex (VLPFC) plays a pivotal role in auditory and audiovisual processing, integration, and mnemonic processing, since VLPFC neurons are responsive to complex acoustic stimuli and are robustly active during auditory WM tasks. Furthermore, inactivation of the VLPFC impairs audiovisual and auditory WM. In these inactivation studies the cortical region that was inactivated by cortical cooling included areas 12/47, 45 and 46 ventral. It is possible that inclusion of area 46 ventral may account for the auditory WM performance deficit previously observed while inactivating VLPFC so further experiments are needed.

methodsIn the present study we examined whether transient inactivation of the DLPFC, including areas 46v and 46d, and 9, in rhesus macaques would effect auditory WM. The DLPFC was inactivated by cortical cooling while two rhesus macaques performed an auditory working memory task. This was followed by permanent ibotenic acid lesions and assessment of behavioral performance post-lesion.

resultsOur experiments demonstrated that inactivation of DLPFC by cortical cooling in two macaques did not result in a significant decrease in performance of an auditory WM task. The inactivation resulted in an increase in dropped gaze events during the latter half of the task, in one subject, which could be due to a loss of attention or motivation. The ibotenic acid lesions of the DLPFC did not significantly alter performance on the auditory WM task.

conclusionsOur results showed that DLPFC transient inactivation with cortical cooling and ibotenic acid lesions did not significantly alter overall auditory working memory performance, which differs from the impairment seen when the VLPFC is inactivated. Our data suggest that the DLPFC and VLPFC may play different roles in auditory working memory.

Indexed as

Auditory PerceptionDorsolateral Prefrontal CortexMemory, Short-TermPrefrontal CortexAcoustic StimulationAnimalsMacaca mulattaMaleauditory discriminationlesionprefrontal cortexvocalizationworking memory

Identifiers

PMID40767011
PMCPMC12880728

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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.