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Chronic Spinal Cord Stimulation Modifies Intrinsic Cardiac Synaptic Efficacy in the Suppression of Atrial Fibrillation

We sought to determine whether spinal cord stimulation (SCS) therapy, when applied chronically to canines, imparts long-lasting cardio-protective effects on neurogenic atrial tachyarrhythmia induction and, if so, whether its effects can be attributable to i) changes in intrinsic cardiac (IC) neuronal transmembrane properties vs ii) modification of their interneuronal stochastic interactivity that initiates such pathology. Data derived from canines subjected to long-term SCS [(group 1: studied after 3-4 weeks SCS; n = 5) (group 2: studied after 5 weeks SCS; n = 11)] were compared to data derived from 10 control animals (including 4 sham SCS electrode implantations). During terminal studies conducted under anesthesia, chronotropic and inotropic responses to vagal nerve or stellate ganglion stimulation were similar in all 3 groups. Chronic SCS suppressed atrial tachyarrhythmia induction evoked by mediastinal nerve stimulation. When induced, arrhythmia durations were shortened (controls: median of 27 s; SCS 3-4 weeks: median of 16 s; SCS 5 weeks: median of 7 s). Phasic and accommodating right atrial neuronal somata displayed similar passive and active membrane properties in vitro, whether derived from sham or either chronic SCS group. Synaptic efficacy was differentially enhanced in accommodating (not phasic) IC neurons by chronic SCS. Taken together these data indicate that chronic SCS therapy modifies IC neuronal stochastic inter-connectivity in atrial fibrillation suppression by altering synaptic function without directly targeting the transmembrane properties of individual IC neuronal somata. •Spinal cord stimulation (SCS) suppresses neurally induced atrial fibrillation (AF).•Effectiveness of SCS in AF suppression increases with time.•SCS minimally impacts active and passive properties of individual intrinsic cardiac neurons.•SCS modifies synaptic efficacy of the IC network.•SCS differentially impacts the neurotransmission to the accommodating sub-population of IC neurons.

Identiferoai:union.ndltd.org:ETSU/oai:dc.etsu.edu:etsu-works-17055
Date01 January 2014
CreatorsArdell, Jeffrey L., Cardinal, René, Beaumont, Eric, Vermeulen, Michel, Smith, Frank M., Andrew Armour, J.
PublisherDigital Commons @ East Tennessee State University
Source SetsEast Tennessee State University
Detected LanguageEnglish
Typetext
SourceETSU Faculty Works

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