Coexistence Of Peripheral Potentiation And Corticospinal Inhibition Following A Conditioning Contraction In Human First Dorsal Interosseous Muscle

In skeletal muscle, postactivation potentiation (PAP) is observed following a conditioning contraction (CC) as a large (two- to three-fold) increase in evoked twitch force and rate of force development (RFD). However, this enhancement has not been observed to occur during potentiated voluntary contractions. The purpose of this study was to determine whether the lack of voluntary potentiation may be related to the development of central (corticospinal) inhibition. Participants (n = 10, all males) completed voluntary and evoked index finger abduction contractions and transcranial magnetic stimulated motor-evoked potentials (MEP) of the motor cortex were recorded from the first dorsal interosseous (FDI). Central inhibition was assessed by measuring the silent period following the MEP. The FDI was potentiated via 10-s conditioning contractions at 60% of maximal index finger abduction strength, using both voluntary and evoked tetanic contractions. Immediately following CC and transcutaneous electrical twitches. Following both voluntary and tetanic CC, force and RFD of the twitch were similarly increased (similar to 200% and similar to 160%, respectively). The silent period was elongated by similar to 10% following both forms of CC. These results indicate that corticospinal inhibition does occur following CC, but that it is unrelated to the voluntary activation during the CC. These results also show that following CC, the positive contractile effects at the muscle are concurrently accompanied by inhibitory effects at the corticospinal level.NEW & NOTEWORTHY We demonstrate that postactivation potentiation in human skeletal muscle is accompanied by central inhibition at the corticospinal level. However, the magnitude of central inhibition does not differ between peripherally evoked or voluntary conditioning contractions. Therefore, it is possible this central inhibition is related to muscle sensory feedback.