Vagus Nerve Stimulation in Ischemic Stroke: Old Wine in a New Bottle

Vagus nerve stimulation (VNS) is currently FDA-approved for treatment of both medically refractory partial-onset seizures and severe, recurrent refractory depression which have failed to respond to medical interventions. Because of its ability to regulate mechanisms well-studied in neuroscience, suc...

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Bibliographic Details
Main Authors: Peter Y Cai, Aakash eBodhit, Roselle eDerequito, Saeed eAnsari-Sadrabadi, Fawzi eAbukhalil, Spandana eThenkabail, Sarah eGanji, Pradeepan eSaravanapavan, Chandana C Shekar, Sharatchandra eBidari, Michael F Waters, Vishnumurthy Shushrutha Hedna
Format: Article
Language:English
Published: Frontiers Media S.A. 2014-06-01
Series:Frontiers in Neurology
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Online Access:http://journal.frontiersin.org/Journal/10.3389/fneur.2014.00107/full
Description
Summary:Vagus nerve stimulation (VNS) is currently FDA-approved for treatment of both medically refractory partial-onset seizures and severe, recurrent refractory depression which have failed to respond to medical interventions. Because of its ability to regulate mechanisms well-studied in neuroscience, such as norepinephrine and serotonin release, the vagus nerve may play an important role in regulating cerebral blood flow, edema, inflammation, glutamate excitotoxicity, and neurotrophic processes. There is strong evidence that these same processes are important in stroke pathophysiology. We reviewed the literature for the role of VNS in improving ischemic stroke outcomes by performing a systematic search for publications in Medline (1966-2014) with keywords vagus nerve stimulation AND stroke in subject headings and key words with no language restrictions. Of the 73 publications retrieved, we identified 7 studies from 3 different research groups that met our final inclusion criteria of research studies addressing the role of vagus nerve stimulation in ischemic stroke. Results from these studies suggest that VNS has promising efficacy in reducing stroke volume and attenuating neurological deficits in ischemic stroke models. Given the lack of success in Phase III trials for stroke neuroprotection, it is important to develop new therapies targeting different neuroprotective pathways. Further studies of the possible role of VNS, through normally physiologically active mechanisms, in ischemic stroke therapeutics should be conducted in both animal models and clinical studies. In addition, recent advent of a non-invasive, transcutaneous VNS could provide the potential for easier clinical translation.
ISSN:1664-2295