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Modulation of spinal cord excitability following remote limb ischemic preconditioning in healthy young men. | LitMetric

Modulation of spinal cord excitability following remote limb ischemic preconditioning in healthy young men.

Exp Brain Res

Laboratory of Signal Processing and Motor Control, LACOMOT, Faculty of Physical Education, Universidade de Brasília, Campus Universitário Darcy Ribeiro, Asa Norte, Brasília, DF, CEP: 70910-900, Brazil.

Published: May 2020

Remote limb ischemic preconditioning (RIPC) has shown to improve dynamic postural control in humans. However, studies on the underlying adaptations of spinal cord networks have never been performed. The present work addresses this issue by investigating parameters from the soleus H-reflex recruitment curve (RC), presynaptic mechanisms of reflex modulation (presynaptic inhibition-PSI, and post activation depression-PAD), and the excursion of the center of pressure (CP) recorded during 1 min in upright stance over a compliant surface. A sham ischemic protocol (partial obstruction of blood flow) was applied to the contralateral thigh along four consecutive days. The same procedure was repeated with full obstruction (RIPC) three days after ending the sham protocol. Data were collected before and after both sham and RIPC protocols. The follow-up data were collected five days after the last ischemic intervention. Significant reduction was detected for both the fast oscillations of the CP (higher frequency components) and the parameter estimated from the RC corresponding to the high amplitude H-reflexes (p < 0.05). Even though the magnitude of effects was similar, it was washed out within three days after sham, but persisted for at least five days after RIPC. No significant differences were found for PSI and PAD levels across conditions. These findings indicate that RIPC leads to enduring changes in spinal cord excitability for the latest reflexively recruited motoneurons, along with improvement in balance control. However, these adaptations were not mediated by the presynaptic mechanisms currently assessed.

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http://dx.doi.org/10.1007/s00221-020-05807-wDOI Listing

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