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Hicks, K. M.

Publications and source records attributed to Hicks, K. M..

2 recordsLinked to original sources

Menstrual cycle phase alters corticospinal excitability and spike-timing-dependent plasticity in healthy females

The known fluctuations in ovarian hormone concentrations across the eumenorrheic menstrual cycle contribute to modulations in cortical excitability and inhibition. However, how such changes affect spike-timing-dependent plasticity (STDP) has not been systematically studied. This research aimed to determine the effect of the menstrual cycle on corticospinal excitability and STDP. Twelve eumenorrheic female participants (age: 25 {+/-} 5 years), visited the lab in three menstrual cycle phases: early follicular (EF), late follicular (LF), and mid-luteal (ML). Visits comprised of corticospinal excitability (motor evoked potential [MEP]/Mmax), short-intracortical inhibition (SICI), and intracortical facilitation (ICF) measures, recorded in the resting first dorsal interosseous. Followed by a paired associative stimulation (PAS) protocol, utilising ulnar nerve and transcranial magnetic stimulation (25 ms interstimulus interval) to elicit neuroplasticity. To assess the time course of STDP, measurements were repeated at 15 and 30-minutes post PAS. Corticospinal excitability (MEP/Mmax) was greater in the LF phase (p[≤]0.002) compared to EF and ML, with no phase effects observed for SICI or ICF (p[≥]0.112). PAS elicited an increase in MEP/Mmax across all phases at 15-minutes (112 {+/-} 5, 115 {+/-} 5, and 113 {+/-} 7% baseline, p[≤]0.010), whereas at 30-minutes only ML was facilitated (126 {+/-} 7% baseline, p=0.029). The present data demonstrates facilitatory STDP can be induced with PAS across the tested menstrual cycle phases, but responses are prolonged and potentiated in the ML phase. Additionally, increased corticospinal excitability in the LF phase is likely due to intrinsic changes within the descending tract, as no changes in intracortical neurotransmission were observed.

neuroscience↗

Sex differences in the cardiopulmonary and neuromuscular response to high-intensity interval exercise

Sex differences exist in the integrative response to exercise, however, these are typically researched during constant-load exercise. Interval exercise involves high-intensity efforts interspersed with recovery periods to repeatedly stress physiological systems, and it is currently unknown whether the response to this form of exercise differs between sexes. Ten males and ten females (age: 25{+/-}3 years) completed two experimental visits. First, an incremental treadmill exercise test was performed to obtain submaximal (lactate threshold) and maximal ([Formula] O2peak) data. Thereafter, visit two involved 4 x 3-min running intervals at 90% of the final incremental test velocity (v[Formula] O2peak), with 90 secs rest between intervals. Before exercise and after each interval, maximal voluntary contraction (MVC), quadriceps potentiated twitch (Qtw.pot), and voluntary activation (VA) were recorded. The rates of oxygen uptake ([Formula] O2), carbon dioxide production ([Formula] CO2) and ventilation ([Formula] E) were continuously recorded throughout. There was no sex difference in relative [Formula] O2peak (males: 47.2{+/-}6.0 vs. females: 44.4{+/-}5.8 ml.kg- 1.min-1, p=0.292). When expressed relative to peak values, there were no sex differences in the [Formula] O2 or [Formula] CO2 response to the interval task (p[≥]0.781). Females had greater [Formula] E, [Formula] E/[Formula] O2, and [Formula] E/[Formula] CO2 values during the first two intervals (p[≤]0.046). There were no sex differences in the reductions in MVC, Qtw.pot, and VA during the interval task (p[≥]0.150), however females had lesser reductions in Qtw.pot values post-exercise (-24{+/-}9 vs. -15{+/-}8%, p=0.044). Sex differences exist in the physiological response to interval exercise. Compared to males, females experienced greater hyperpnoea during the initial stages, and had lesser decreases in contractile function post-exercise.

physiology↗