Short-latency afferent inhibition is a poor predictor of individual susceptibility to rTMS-induced plasticity in the motor cortex of young and older adults

• Published in: Frontiers in aging neuroscience Vol. 6; p. 182
• Main Authors: Young-Bernier, Marielle, Tanguay, Annick N, Davidson, Patrick S R, Tremblay, François
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Research Foundation 07.08.2014; Frontiers Media S.A
• Subjects: Age; Age differences; Aging; Brain research; Cholinergic function; Cholinergic transmission; Cortex (motor); Latency; Long-term potentiation; Magnetic fields; Median nerve; Motor evoked potentials; Neural plasticity; Neuroscience; Older people; Sensory neurons; Short afferent inhibition; theta burst; Transcranial Magnetic Stimulation; Young adults; cholinergic function; aging; transcranial magnetic stimulation; theta burst; short afferent inhibition
• ISSN: 1663-4365; 1663-4365
• DOI: 10.3389/fnagi.2014.00182

Cortical plasticity, including long-term potentiation (LTP)-like plasticity, can be assessed non-invasively with repetitive transcranial magnetic stimulation (rTMS) protocols. In this study, we examined age differences in responses to intermittent theta burst stimulation (iTBS) in a group of 20 young and 18 healthy older adults. Because the cholinergic system plays a role in the neural processes underlying learning and memory, including LTP, we also investigated whether short latency afferent inhibition (SAI), a neurophysiological marker of central cholinergic activity, would be associated with age-related differences in LTP-like plasticity induced by iTBS. SAI was first assessed by examining the modulation of motor evoked potentials (MEPs) in response to median nerve conditioning 20 ms prior to TMS. Participants then underwent iTBS (3 pulses at 50 Hz every 200 ms for 2 s with 8 s between trains, repeated 20 times). MEP responses (120% resting motor threshold (RMT)) were assessed immediately after iTBS and 5, 10, and 20 min post-application. Responses to iTBS were quite variable in both age groups, with only approximately 60% of the participants (n = 13 young and 10 older adults) showing the expected facilitation of MEP responses. There were no significant age group differences in MEP facilitation following iTBS. Although older adults exhibited reduced SAI, individual variations were not associated with susceptibility to express LTP-like induced plasticity after iTBS. Overall, these results are consistent with reports of high inter-individual variability in responses to iTBS. Although SAI was reduced in older adults, consistent with a deterioration of the cholinergic system with age, SAI levels were not associated with LTP-like plasticity as assessed with iTBS.