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Transcutaneous auricular vagus nerve stimulation modifies cortical excitability in middle-aged and older adults
Journal article   Open access   Peer reviewed

Transcutaneous auricular vagus nerve stimulation modifies cortical excitability in middle-aged and older adults

Ashraf N H Gerges, Lynton Graetz, Susan Hillier, Jeric Uy, Taya Hamilton, George Opie, Ann-Maree Vallence, Felicity A Braithwaite, Saran Chamberlain and Brenton Hordacre
Psychophysiology, Vol.62(1), e14584
2024
PMID: 38602055
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CC BY-NC-ND V4.0 Open Access

Abstract

auricular vagus nerve stimulation vagus nerve TMS aging cortical excitability neuroplasticity
There is a growing interest in the clinical application of transcutaneous auricular vagus nerve stimulation (taVNS). However, its effect on cortical excitability, and whether this is modulated by stimulation duration, remains unclear. We evaluated whether taVNS can modify excitability in the primary motor cortex (M1) in middle-aged and older adults and whether the stimulation duration moderates this effect. In addition, we evaluated the blinding efficacy of a commonly reported sham method. In a double-blinded randomized cross-over sham-controlled study, 23 healthy adults (mean age 59.91 ± 6.87 years) received three conditions: active taVNS for 30 and 60 min and sham for 30 min. Single and paired-pulse transcranial magnetic stimulation was delivered over the right M1 to evaluate motor-evoked potentials. Adverse events, heart rate and blood pressure measures were evaluated. Participant blinding effectiveness was assessed via guesses about group allocation. There was an increase in short-interval intracortical inhibition (F = 7.006, p = .002) and a decrease in short-interval intracortical facilitation (F = 4.602, p = .014) after 60 min of taVNS, but not 30 min, compared to sham. taVNS was tolerable and safe. Heart rate and blood pressure were not modified by taVNS (p > .05). Overall, 96% of participants detected active stimulation and 22% detected sham stimulation. taVNS modifies cortical excitability in M1 and its effect depends on stimulation duration in middle-aged and older adults. taVNS increased GABAAergic inhibition and decreased glutamatergic activity. Sham taVNS protocol is credible but there is an imbalance in beliefs about group allocation.

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Citation topics
1 Clinical & Life Sciences
1.222 Epilepsy & Seizures
1.222.542 Epilepsy Mechanisms
Web Of Science research areas
Neurosciences
Physiology
Psychology
Psychology, Biological
Psychology, Experimental
ESI research areas
Psychiatry/Psychology
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