Acute exercise as a modifier of neocortical plasticity and aperiodic activity in the visual cortex

Claire J. Cadwallader, Jennifer Steiniger, Patrick S. Cooper, Shou-Han Zhou, Joshua Hendrikse, Rachael L. Sumner, Ian J. Kirk, Trevor T.J. Chong, James P. Coxon

Research output: Contribution to journalArticleResearchpeer-review

3 Citations (Scopus)

Abstract

Long-term potentiation (LTP) is a form of neuroplasticity commonly implicated in mechanistic models of learning and memory. Acute exercise can boost LTP in the motor cortex, and is associated with a shift in excitation/inhibition (E:I) balance, but whether this extends to other regions such as the visual cortex is unknown. We investigated the effect of a preceding bout of exercise on LTP induction and the E:I balance in the visual cortex using electroencephalography (EEG). Young adults (N = 20, mean age = 24.20) engaged in 20 min of high-intensity interval training (HIIT) exercise and rest across two counterbalanced sessions. LTP was induced using a high frequency presentation of a visual stimulus; a “visual tetanus”. Established EEG markers of visual LTP, the N1b and P2 component of the visual evoked potential, and an EEG-derived measure of the E:I balance, the aperiodic exponent, were measured before and after the visual tetanus. As expected, there was a potentiation of the N1b following the visual tetanus, with specificity to the tetanised stimulus, and a non-specific potentiation of the P2. These effects were not sensitive to a preceding bout of exercise. However, the E:I balance showed a late shift towards inhibition following the visual tetanus. A preceding bout of exercise resulted in specificity of this E:I balance shift to the tetanised stimulus, that was not seen following rest. This novel finding suggests a possible exercise-induced tuning of the visual cortex to stimulus details following LTP induction.

Original languageEnglish
Article number7491
Number of pages11
JournalScientific Reports
Volume13
Issue number1
DOIs
Publication statusPublished - Dec 2023

Cite this