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Spinal cord stimulation suppresses bradycardias and atrial tachyarrhythmias induced by mediastinal nerve stimulation in dogs.

Spinal cord stimulation suppresses bradycardias and atrial tachyarrhythmias induced by mediastinal nerve stimulation in dogs. Research Abstract Details 

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  • Spinal cord stimulation suppresses bradycardias and atrial tachyarrhythmias induced by mediastinal nerve stimulation in dogs. Abstract Text:

     cardinal Cardinal,pierre Pierre ,michel vermeulenMichel Vermeulen,caroline bouchardCaroline Bouchard,jeffrey l ardellJeffrey L Ardell,robert d foremanRobert D Foreman,j andrew armourJ Andrew Armour,

    Spinal cord stimulation (SCS) applied to the dorsal aspect of the cranial thoracic cord imparts cardioprotection under conditions of neuronally dependent cardiac stress. This study investigated whether neuronally induced atrial arrhythmias can be modulated by SCS. In 16 anesthetized dogs with intact stellate ganglia and in five with bilateral stellectomy, trains of five electrical stimuli were delivered during the atrial refractory period to right- or left-sided mediastinal nerves for up to 20 s before and after SCS (20 min). Recordings were obtained from 191 biatrial epicardial sites. Before SCS (11 animals), mediastinal nerve stimulation initiated bradycardia alone (12 nerve sites), bradycardia followed by tachyarrhythmia/fibrillation (50 sites), as well as tachyarrhythmia/fibrillation without a preceding bradycardia (21 sites). After SCS, the number of responsive sites inducing bradycardia was reduced by 25% (62 to 47 sites), and the cycle length prolongation in residual bradycardias was reduced. The number of responsive sites inducing tachyarrhythmia was reduced by 60% (71 to 29 sites). Once elicited, residual tachyarrhythmias arose from similar epicardial foci, displaying similar dynamics (cycle length) as in control states. In the absence of SCS, bradycardias and tachyarrhythmias induced by repeat nerve stimulation were reproducible (five additional animals). After bilateral stellectomy, SCS no longer influenced neuronal induction of bradycardia and atrial tachyarrhythmias. These data indicate that SCS obtunds the induction of atrial arrhythmias resulting from excessive activation of intrinsic cardiac neurons and that such protective effects depend on the integrity of nerves coursing via the subclavian ansae and stellate ganglia.

    Spinal cord stimulation suppresses bradycardias and atrial tachyarrhythmias induced by mediastinal nerve stimulation in dogs. Publishing Authors By Initials

    r cardinalR Cardinal,p P ,m vermeulenM Vermeulen,c bouchardC Bouchard,jl ardellJL Ardell,rd foremanRD Foreman,ja armourJA Armour,

    For similar cardiovascular diseases: heart diseases: arrhythmias, cardiac: tachycardia research abstracts see: cardiovascular diseases: heart diseases: arrhythmias, cardiac: tachycardia research

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    Spinal cord stimulation suppresses bradycardias and atrial tachyarrhythmias induced by mediastinal nerve stimulation in dogs. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: American journal of physiology. Regulatory, integr

    VOLUME: 291

    Page Numbers: R1369-75

    Journal Abbreviation: Am. J. Physiol. Regul. Integr.

    ISSN: 0363-6119

    DAY: 15

    MONTH: 06

    YEAR: 2006

    Spinal cord stimulation suppresses bradycardias and atrial tachyarrhythmias induced by mediastinal nerve stimulation in dogs. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 100901230

    Spinal cord stimulation suppresses bradycardias and atrial tachyarrhythmias induced by mediastinal nerve stimulation in dogs. Keywords Mesh Terms:

    KEYWORDS: Tachycardia

    MESH TERMS: physiopathology

    Chemical & Substance for Abstract: Spinal cord stimulation suppresses bradycardias and atrial tachyarrhythmias induced by mediastinal nerve stimulation in dogs. Information

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    Grant and Affiliation Information for Spinal cord stimulation suppresses bradycardias and atrial tachyarrhythmias induced by mediastinal nerve stimulation in dogs.

    AFFILIATION: Centre de Recherche, Hôpital du Sacré-Coeur de Montréal and Faculté de Médecine, Université de Montréal, Québec, Canada H4J 1C5. rene.cardinal@umontreal.ca

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NHLBI

    GRANT: HL71830

    ACRONYM: HL

    MEDLINETA: Am J Physiol Regul Integr Comp

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