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Shengcui Cheng

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YNIMG Journal 2026 Journal Article

Transcutaneous auricular vagus nerve stimulation facilitates visuomotor association learning: Behavioral and electrophysiological evidence

  • Long Chen
  • Chenghu Tang
  • Huixin Gao
  • Lei Zhang
  • Shengcui Cheng
  • Zhongpeng Wang
  • Shuang Liu
  • Dong Ming

Associating visual cues with appropriate motor responses is a fundamental adaptive skill. Transcutaneous auricular vagus nerve stimulation (taVNS) may enhance visuomotor association (VMA) learning, though its neural mechanisms remain unclear. Electroencephalogram (EEG), with its millisecond temporal resolution, offers unique advantages for elucidating the neurodynamic of VMA plasticity. This single-blind, sham-controlled, between-subjects study investigated whether taVNS facilitates VMA learning through behavioral and EEG analysis. Participants (each group N = 19) performed a VMA task (associating five oracle pictures with five keyboard keys) before and after 20-min active/sham taVNS. Behavioral results revealed that compared to the sham group, the active group exhibited shorter reaction time, higher response accuracy and larger learning curve integration, confirming the positive effect of taVNS on VMA learning. Neurophysiologically, taVNS reduced the P200 and P300 amplitudes, enhanced N170 negativity and attenuated error-related negativity. Cross-regional-frequency phase-amplitude coupling results demonstrated enhanced synchronization of frontal-parietal-occipital neural cross-frequency activity. Additionally, parietal-occipital θ, α, β band inter-trial phase coherence was enhanced in the active group. These findings demonstrate that taVNS enhances VMA acquisition through optimizing visual and error processing efficiency. This study establishes a neurophysiological basis for taVNS's cognitive enhancement potential, suggesting its utility in rehabilitative paradigms targeting associative learning deficits.

YNICL Journal 2018 Journal Article

Abnormal functional corticomuscular coupling after stroke

  • Xiaoling Chen
  • Ping Xie
  • Yuanyuan Zhang
  • Yuling Chen
  • Shengcui Cheng
  • Litai Zhang

Motor dysfunction is a major consequence after stroke and it is generally believed that the loss of motor ability is caused by the impairments in neural network that controls movement. To explore the abnormal mechanisms how the brain controls shoulder abduction and elbow flexion in "flexion synergy" following stroke, we used the functional corticomuscular coupling (FCMC) between the brain and the muscles as a tool to identify the temporal evolution of corticomuscular interaction between the synkinetic and separate phases. 59-channel electroencephalogram (EEG) over brain scalp and 2-channel electromyogram (EMG) from biceps brachii (BB)/deltoid (DT) were recorded in sixteen stroke patients with motor dysfunction and eight healthy controls during a task of uplifting the arm (stage 1) and maintaining up to the chest (stage 2). As a result, compared to healthy controls, stroke patients had abnormally reduced coherence in EEG-BB combination and increased coherence in EEG-DT combination. Compared to synkinetic stroke patients, separate ones exhibited higher coupling at gamma-band during stage 1 and higher at beta-band during stage 2 in EEG-BB combination, but lower at beta-band during stage 2 in EEG-DT combination. Therefore, we infer that the disorders of efferent control and afferent proprioception in sensorimotor system for stroke patients effect on the oscillation at beta and gamma bands. Patients need integrate more information for shoulder abduction to compensate for the functional loss of elbow flexion in the recovery process, so that partial cortical cortex controlling on the elbow flexion may work on the shoulder abduction during "flexion synergy". Such researches could provide new perspective on the temporal evolution of corticomuscular interaction after stroke and add to our understanding of possible pathomechanisms how the brain abnormally controls shoulder abduction and elbow flexion in "flexion synergy".

v2026.09.13