Journal
PHYSIOLOGICAL REPORTS
Volume 10, Issue 8, Pages -Publisher
WILEY
DOI: 10.14814/phy2.15257
Keywords
autonomic nervous system; bioelectric medicine; directional stimulation; medical devices; metabolic disease; selective peripheral nerve stimulation
Categories
Funding
- Bionics Institute Incubation Fund
- St. Vincent's Research Endowment Fund [85257]
- Cass Foundation Limited [8511]
- University of Melbourne [1757246]
- Victorian Government through its Operational Infrastructural Support Program
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Vagus nerve stimulation has shown promise as a treatment for type 2 diabetes. This study demonstrated that stimulation of the abdominal vagus nerve in metabolically compromised rats can effectively decrease glycemia without causing damage to the nerve tissue. The findings suggest that further development of this therapy could lead to a novel treatment for type 2 diabetes.
Vagus nerve stimulation is emerging as a promising treatment for type 2 diabetes. Here, we evaluated the ability of stimulation of the vagus nerve to reduce glycemia in awake, freely moving metabolically compromised rats. A model of type 2 diabetes (n = 10) was induced using a high-fat diet and low doses of streptozotocin. Stimulation of the abdominal vagus nerve was achieved by pairing 15 Hz pulses on a distal pair of electrodes with high-frequency blocking stimulation (26 kHz, 4 mA) on a proximal pair of electrodes to preferentially produce efferent conducting activity (eVNS). Stimulation was well tolerated in awake, freely moving rats. During 1 h of eVNS, glycemia decreased in 90% of subjects (-1.25 +/- 1.25 mM h, p = 0.017), and 2 dB above neural threshold was established as the most effective dose of eVNS (p = 0.009). Following 5 weeks of implantation, eVNS was still effective, resulting in significantly decreased glycemia (-1.7 +/- 0.6 mM h, p = 0.003) during 1 h of eVNS. There were no overt changes in fascicle area or signs of histopathological damage observed in implanted vagal nerve tissue following chronic implantation and stimulation. Demonstration of the biocompatibility and safety of eVNS in awake, metabolically compromised animals is a critical first step to establishing this therapy for clinical use. With further development, eVNS could be a promising novel therapy for treating type 2 diabetes.
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