The effects of caffeine on short-latency afferent inhibition measured with paired-pulse conventional and threshold-tracking TMS


Carrozzo C., Cannazza M., Fratini D., Fanella G., CENGİZ B., Lazzaro V. D., ...Daha Fazla

Clinical Neurophysiology, cilt.187, 2026 (SCI-Expanded, Scopus) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 187
  • Basım Tarihi: 2026
  • Doi Numarası: 10.1016/j.clinph.2026.2111857
  • Dergi Adı: Clinical Neurophysiology
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, BIOSIS, EMBASE, MEDLINE
  • Anahtar Kelimeler: Caffeine, threshold-tracking SAI, SAI, Short-latency afferent inhibition, Transcranial magnetic stimulation
  • Gazi Üniversitesi Adresli: Evet

Özet

Objective: Transcranial Magnetic Stimulation (TMS) tests of Short-latency Afferent Inhibition (SAI) by conventional amplitude (A-SAI) and threshold-tracking (T-SAI) are important methods to investigate cortical excitability and, more specifically, sensory motor-integration. Since beverages containing caffeine are widely consumed, and caffeine has been reported to affect cortical excitability, it is of interest to explore if SAI is modulated by caffeine. Methods: Twenty healthy subjects (11 females, 9 males; mean age: 27.0 ± 5.53) were studied in a single fixed-dose randomized double-blind placebo-controlled cross-over trial of 200 mg caffeine or placebo administered as chewing gum. Changes in A-SAI and T-SAI at 12 interstimulus intervals between 18 ms and 30 ms were assessed by conventional fixed stimulus and threshold-tracking techniques. Results: There was no effect of caffeine on SAI across the full range of ISIs with either of the methods. However, caffeine significantly enhanced peak A-SAI (ISIs 19–21 ms) when compared to placebo (p = 0.011), while no effect on peak T-SAI was found. Conclusion: Caffeine enhances SAI as evaluated with the conventional A-SAI protocol, but not with the threshold-tracking method. Significance: Caffeinés effect may result from its modulation of the cholinergic system, providing insights into both its physiological action and brain disorder pathophysiology.