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Does trans-spinal and local DC polarization affect presynaptic inhibition and post-activation depression?

Journal article
Authors Dominik Kaczmarek
Joel Ristikankare
Elzbieta Jankowska
Published in Journal of Physiology
Volume 595
Issue 5
Pages 1743-1761
ISSN 0022-3751
Publication year 2017
Published at Institute of Neuroscience and Physiology
Pages 1743-1761
Language en
Keywords soleus h-reflex, ii muscle afferents, postactivation depression, cutaneous afferents, synaptic action, cord, stimulation, depolarization, cat, Neurosciences & Neurology, Physiology
Subject categories Neurosciences, Physiology


Direct current (DC) polarization has been demonstrated to alleviate the effects of various deficits in the operation of the central nervous system. However, the effects of trans-spinal DC stimulation (tsDCS) have been investigated less extensively than the effects of transcranial DC stimulation, and their cellular mechanisms have not been elucidated. The main objectives of this study were, therefore, to extend our previous analysis of DC effects on the excitability of primary afferents and synaptic transmission by examining the effects of DC on two spinal modulatory feedback systems, presynaptic inhibition and post-activation depression, in an anaesthetized rat preparation. Other objectives were to compare the effects of locally and trans-spinally applied DC(locDC and tsDCS). Local polarization at the sites of terminal branching of afferent fibres was found to induce polarity-dependent actions on presynaptic inhibition and post-activation depression, as cathodal locDC enhanced them and anodal locDC depressed them. In contrast, tsDCS modulated presynaptic inhibition and post-activation depression in a polarity-independent fashion because both cathodal and anodal tsDCS facilitated them. The results show that the local presynaptic actions of DC might counteract both excessively strong and excessively weak monosynaptic actions of group Ia and cutaneous afferents. However, they indicate that trans-spinally applied DC might counteract the exaggerated spinal reflexes but have an adverse effect on pathologically weakened spinal activity by additional presynaptic weakening. The results are also relevant for the analysis of the basic properties of presynaptic inhibition and post-activation depression because they indicate that some common DC-sensitive mechanisms contribute to them.

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