Drug‐Responsive Inhomogeneous Cortical Modulation by Direct Current Stimulation
Autor: | Marti Goldenberg, Javier Márquez-Ruiz, Joseph R. Madsen, Alvaro Pascual-Leone, Ricardo Salvador, Sameer C. Dhamne, Giulio Ruffini, Brianna Godlewski, Yan Sun, Alexander Rotenberg, Scellig S D Stone, Alejandro Carretero-Guillén |
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Rok vydání: | 2020 |
Předmět: |
Male
0301 basic medicine Kainic acid Stimulation Transcranial Direct Current Stimulation Somatosensory system Mice 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine medicine Animals Humans Cerebral Cortex Epilepsy Neocortex Long-Term Synaptic Depression Glutamate receptor Long-term potentiation Mice Inbred C57BL 030104 developmental biology medicine.anatomical_structure Neurology chemistry NMDA receptor Neurology (clinical) Excitatory Amino Acid Antagonists Neuroscience 030217 neurology & neurosurgery Motor cortex |
Zdroj: | Annals of Neurology. 88:489-502 |
ISSN: | 1531-8249 0364-5134 |
DOI: | 10.1002/ana.25822 |
Popis: | Objective Cathodal direct current stimulation (cDCS) induces long-term depression (LTD)-like reduction of cortical excitability (DCS-LTD), which has been tested in the treatment of epilepsy with modest effects. In part, this may be due to variable cortical neuron orientation relative to the electric field. We tested, in vivo and in vitro, whether DCS-LTD occurs throughout the cortical thickness, and if not, then whether drug-DCS pairing can enhance the uniformity of the cortical response and the cDCS antiepileptic effect. Methods cDCS-mediated changes in cortical excitability were measured in vitro in mouse motor cortex (M1) and in human postoperative neocortex, in vivo in mouse somatosensory cortex (S1), and in a mouse kainic acid (KA)-seizure model. Contributions of N-methyl-D-aspartate-type glutamate receptors (NMDARs) to cDCS-mediated plasticity were tested with application of NMDAR blockers (memantine/D-AP5). Results cDCS reliably induced DCS-LTD in superficial cortical layers, and a long-term potentiation (LTP)-like enhancement (DCS-LTP) was recorded in deep cortical layers. Immunostaining confirmed layer-specific increase of phospho-S6 ribosomal protein in mouse M1. Similar nonuniform cDCS aftereffects on cortical excitability were also found in human neocortex in vitro and in S1 of alert mice in vivo. Application of memantine/D-AP5 either produced a more uniform DCS-LTD throughout the cortical thickness or at least abolished DCS-LTP. Moreover, a combination of memantine and cDCS suppressed KA-induced seizures. Interpretation cDCS aftereffects are not uniform throughout cortical layers, which may explain the incomplete cDCS clinical efficacy. NMDAR antagonists may augment cDCS efficacy in epilepsy and other disorders where regional depression of cortical excitability is desirable. ANN NEUROL 2020;88:489-502. |
Databáze: | OpenAIRE |
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