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Non-invasive electroencephalography in awake cats: Feasibility and application to sensory processing in chronic pain.
Delsart, Aliénor; Castel, Aude; Dumas, Guillaume; Otis, Colombe; Lachance, Mathieu; Barbeau-Grégoire, Maude; Lussier, Bertrand; Péron, Franck; Hébert, Marc; Lapointe, Nicolas; Moreau, Maxim; Martel-Pelletier, Johanne; Pelletier, Jean-Pierre; Troncy, Eric.
Affiliation
  • Delsart A; Groupe de recherche en pharmacologie animale du Québec (GREPAQ), Université de Montréal, Québec, Canada.
  • Castel A; Groupe de recherche en pharmacologie animale du Québec (GREPAQ), Université de Montréal, Québec, Canada; Department of clinical sciences, Faculté de médecine vétérinaire, Université de Montréal, Québec, Canada. Electronic address: aude.castel@umontreal.ca.
  • Dumas G; Department of psychiatry and addictology, Faculté de médecine, Université de Montréal, Québec, Canada; Research center of the Sainte-Justine mother and child university hospital center (CHU Sainte-Justine), Québec, Canada.
  • Otis C; Groupe de recherche en pharmacologie animale du Québec (GREPAQ), Université de Montréal, Québec, Canada.
  • Lachance M; Groupe de recherche en pharmacologie animale du Québec (GREPAQ), Université de Montréal, Québec, Canada.
  • Barbeau-Grégoire M; Groupe de recherche en pharmacologie animale du Québec (GREPAQ), Université de Montréal, Québec, Canada.
  • Lussier B; Groupe de recherche en pharmacologie animale du Québec (GREPAQ), Université de Montréal, Québec, Canada; Department of clinical sciences, Faculté de médecine vétérinaire, Université de Montréal, Québec, Canada; Osteoarthritis research unit, University of Montreal hospital research center (CRCHUM), Q
  • Péron F; Parc de la Chapelle, Plescop, France.
  • Hébert M; Department of ophthalmology and otorhinolaryngology - Head and neck surgery, Faculté de médecine, Université Laval, Québec, Canada; CERVO Brain Research Center, Québec, Canada.
  • Lapointe N; Zilia Inc., Québec, Canada.
  • Moreau M; Groupe de recherche en pharmacologie animale du Québec (GREPAQ), Université de Montréal, Québec, Canada; Osteoarthritis research unit, University of Montreal hospital research center (CRCHUM), Québec, Canada.
  • Martel-Pelletier J; Groupe de recherche en pharmacologie animale du Québec (GREPAQ), Université de Montréal, Québec, Canada; Osteoarthritis research unit, University of Montreal hospital research center (CRCHUM), Québec, Canada.
  • Pelletier JP; Groupe de recherche en pharmacologie animale du Québec (GREPAQ), Université de Montréal, Québec, Canada; Osteoarthritis research unit, University of Montreal hospital research center (CRCHUM), Québec, Canada.
  • Troncy E; Groupe de recherche en pharmacologie animale du Québec (GREPAQ), Université de Montréal, Québec, Canada; Osteoarthritis research unit, University of Montreal hospital research center (CRCHUM), Québec, Canada.
J Neurosci Methods ; 411: 110254, 2024 Nov.
Article in En | MEDLINE | ID: mdl-39173717
ABSTRACT

BACKGROUND:

Feline osteoarthritis (OA) leads to chronic pain and somatosensory sensitisation. In humans, sensory exposure can modulate chronic pain. Recently, electroencephalography (EEG) revealed a specific brain signature to human OA. However, EEG pain characterisation or its modulation does not exist in OA cats, and all EEG were conducted in sedated cats, using intradermal electrodes, which could alter sensory (pain) perception. NEW

METHOD:

Cats (n=11) affected by OA were assessed using ten gold-plated surface electrodes. Sensory stimuli were presented in random orders response to mechanical temporal summation, grapefruit scent and mono-chromatic wavelengths (500 nm-blue, 525 nm-green and 627 nm-red light). The recorded EEG was processed to identify event-related potentials (ERP) and to perform spectral analysis (z-score).

RESULTS:

The procedure was well-tolerated. The ERPs were reported for both mechanical (F3, C3, Cz, P3, Pz) and olfactory stimuli (Cz, Pz). The main limitation was motion artifacts. Spectral analysis revealed a significant interaction between the power of EEG frequency bands and light wavelengths (p<0.001). All wavelengths considered, alpha band proportion was higher than that of delta and gamma bands (p<0.044), while the latter was lower than the beta band (p<0.016). Compared to green and red, exposure to blue light elicited distinct changes in EEG power over time (p<0.001). COMPARISON WITH EXISTING

METHOD:

This is the first demonstration of EEG feasibility in conscious cats with surface electrodes recording brain activity while exposing them to sensory stimulations.

CONCLUSION:

The identification of ERPs and spectral patterns opens new avenues for investigating feline chronic pain and its potential modulation through sensory interventions.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Wakefulness / Feasibility Studies / Electroencephalography / Chronic Pain Limits: Animals Language: En Journal: J Neurosci Methods Year: 2024 Document type: Article Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Wakefulness / Feasibility Studies / Electroencephalography / Chronic Pain Limits: Animals Language: En Journal: J Neurosci Methods Year: 2024 Document type: Article Country of publication: