Effects of ketamine on frontoparietal interactions during working memory in macaque monkeys
Liya Ma, Nupur Katyare, Kevin Johnston, Stefan Everling
bioRxiv Preprint Server May 16, 2023 preprint DOI: 10.1101/2023.05.16.540957 (opens in new tab)
Study at a glance
AI-extracted from the abstract| Characteristics | Preclinical experimental study |
|---|---|
| Population | Macaque monkeys |
| Intervention | Ketamine |
| Dose | low doses |
| Topics | Ketamine Esketamine |
| Keywords | Neuroscience: brain function Cognitive neuroscience Neural networks Neurobiology Brain communication Working memory Brain dysconnection Brain disorders Neuropsychiatric conditions Cognitive disorders Schizophrenia Pharmacology: psychopharmacology Drug research Medication effects Neuropharmacology Translational research Monkeys Treatment development: therapeutics Drug discovery Medical research New treatments |
| Key findings | Ketamine impairs working memory by disrupting neural coding and reducing frontoparietal connectivity and coherence in macaque monkeys. |
Abstract
Schizophrenia is known as a syndrome of dysconnection among brain regions. As a model for this syndrome, low doses of N-methyl-D-aspartate (NMDA) receptor antagonists, such as ketamine, produce schizophrenia-like symptoms and cognitive deficits in healthy humans and animals. One of such deficits is impaired working memory, a process that engages an extended network of both frontal and parietal areas. While ketamine is known to disrupt working memory by altering both spiking and oscillatory activities in the lateral prefrontal cortex (lPFC), it remains unknown whether NMDA receptor antagonists also produce frontoparietal dysconnection during working memory processes. Here, we simultaneously recorded both single unit activities and local field potentials from lPFC and posterior parietal cortex (PPC) in macaque monkeys during a rule-based working memory task. Like previous work in the lPFC alone, we found that ketamine compromised delay-period rule coding in single neurons and reduced low-frequency oscillations in the PPC. Furthermore, ketamine reduced task-related connectivity in both fronto-parietal and parieto-frontal directions. Consistent with this, ketamine also weakened interareal coherence between spiking and low-frequency oscillatory activities. Our findings demonstrate the utility of acute NMDA receptor antagonist in simulating a syndrome of dysconnection and support this model in its potential for the exploration of novel treatment strategies for schizophrenia.