TY - JOUR
T1 - Effects of acute intermittent hypoxia on corticospinal excitability within the primary motor cortex
AU - Radia, Shivani
AU - Vallence, Ann-Maree
AU - Fujiyama, Hakuei
AU - Fitzpatrick, Rose
AU - Etherington, Sarah
AU - Scott, Brendan R.
AU - Girard, Olivier
PY - 2022/9
Y1 - 2022/9
N2 - Purpose Acute intermittent hypoxia (AIH) is a safe and non-invasive treatment approach that uses brief, repetitive periods of breathing reduced oxygen air alternated with normoxia. While AIH is known to affect spinal circuit excitability, the effects of AIH on cortical excitability remain largely unknown. We investigated the effects of AIH on cortical excitability within the primary motor cortex.Methods Eleven healthy, right-handed participants completed two testing sessions: (1) AIH (comprising 3 min in hypoxia [fraction of inspired oxygen similar to 10%] and 2 min in normoxia repeated over five cycles) and (2) normoxia (NOR) (equivalent duration to AIH). Single- and paired-pulse transcranial magnetic stimulations were delivered to the primary motor cortex, before and 0, 25, and 50 min after AIH and normoxia.Results The mean nadir in arterial oxygen saturation was lower (p < 0.001) during the cycles of AIH (82.5 +/- 4.9%) than NOR (97.8 +/- 0.6%). There was no significant difference in corticospinal excitability, intracortical facilitation, or intracortical inhibition between AIH and normoxia conditions at any time point (all p > 0.05). There was no association between arterial oxygen saturation and changes in corticospinal excitability after AIH (r = 0.05, p = 0.87).Conclusion Overall, AIH did not modify either corticospinal excitability or excitability of intracortical facilitatory and inhibitory circuits within the primary motor cortex. Future research should explore whether a more severe or individualised AIH dose would induce consistent, measurable changes in corticospinal excitability.
AB - Purpose Acute intermittent hypoxia (AIH) is a safe and non-invasive treatment approach that uses brief, repetitive periods of breathing reduced oxygen air alternated with normoxia. While AIH is known to affect spinal circuit excitability, the effects of AIH on cortical excitability remain largely unknown. We investigated the effects of AIH on cortical excitability within the primary motor cortex.Methods Eleven healthy, right-handed participants completed two testing sessions: (1) AIH (comprising 3 min in hypoxia [fraction of inspired oxygen similar to 10%] and 2 min in normoxia repeated over five cycles) and (2) normoxia (NOR) (equivalent duration to AIH). Single- and paired-pulse transcranial magnetic stimulations were delivered to the primary motor cortex, before and 0, 25, and 50 min after AIH and normoxia.Results The mean nadir in arterial oxygen saturation was lower (p < 0.001) during the cycles of AIH (82.5 +/- 4.9%) than NOR (97.8 +/- 0.6%). There was no significant difference in corticospinal excitability, intracortical facilitation, or intracortical inhibition between AIH and normoxia conditions at any time point (all p > 0.05). There was no association between arterial oxygen saturation and changes in corticospinal excitability after AIH (r = 0.05, p = 0.87).Conclusion Overall, AIH did not modify either corticospinal excitability or excitability of intracortical facilitatory and inhibitory circuits within the primary motor cortex. Future research should explore whether a more severe or individualised AIH dose would induce consistent, measurable changes in corticospinal excitability.
KW - Acute intermittent hypoxia
KW - Corticospinal excitability
KW - Transcranial magnetic stimulation
KW - Primary motor cortex
KW - Intracortical inhibition
KW - TRANSCRANIAL MAGNETIC STIMULATION
KW - LONG-TERM FACILITATION
KW - I WAVE INTERACTION
KW - GENOMIC CONSEQUENCES
KW - PLASTICITY
KW - INHIBITION
KW - MODULATION
KW - MECHANISMS
KW - INTACT
UR - http://www.scopus.com/inward/record.url?scp=85132795261&partnerID=8YFLogxK
U2 - 10.1007/s00421-022-04982-8
DO - 10.1007/s00421-022-04982-8
M3 - Article
C2 - 35752660
SN - 1439-6319
VL - 122
SP - 2111
EP - 2123
JO - European Journal of Applied Physiology
JF - European Journal of Applied Physiology
IS - 9
ER -