Therapeutic effect of non-invasive vagus nerve stimulation in gait disturbance and freezing in Parkinson’s disease patients

2018 ◽  
Vol 46 ◽  
pp. e21 ◽  
Author(s):  
B. Mondal ◽  
S. Choudhury ◽  
K. Chatterjee ◽  
R. Banerjee ◽  
S. Shubham ◽  
...  
2021 ◽  
Vol 7 (1) ◽  
Author(s):  
Banashree Mondal ◽  
Supriyo Choudhury ◽  
Rebecca Banerjee ◽  
Akash Roy ◽  
Koustav Chatterjee ◽  
...  

AbstractNon-invasive vagus nerve stimulation (nVNS) is an established neurostimulation therapy used in the treatment of epilepsy, migraine and cluster headache. In this randomized, double-blind, sham-controlled crossover trial we explored the role of nVNS in the treatment of gait and other motor symptoms in Parkinson’s disease (PD) patients. In a subgroup of patients, we measured selected neurotrophin levels and markers of inflammation and oxidative stress in serum, before and after the experimental intervention. Thirty-three PD patients with associated freezing of gait were randomised to either nVNS or sham. After baseline assessments, patients were instructed to deliver 6 two-minute stimulations (total 12 min/day) of the nVNS/sham device (electroCore, Inc. USA) for one month at home. Patients were then re-assessed. After a washout period of one month, the same patients were allocated to the alternate treatment arm and the same process was followed. Significant improvements in key gait parameters were observed with nVNS, including walking speed, stance time and step length, compared to sham. Similarly, overall motor function (MDS-UPDRS III) also improved significantly following nVNS stimulation. Serum Tumor Necrosis Factor (TNF)-α and glutathione levels decreased and brain-derived neurotrophic factor (BDNF) levels increased significantly (p < 0.05) after treatment with nVNS. Here we present the first double-blind sham-controlled trial evidence of the efficacy and safety of nVNS in the treatment of gait and motor function in patients with PD.


2020 ◽  
Vol 13 (5) ◽  
pp. 1323-1332 ◽  
Author(s):  
Ariana Q. Farrand ◽  
Ryan S. Verner ◽  
Ryan M. McGuire ◽  
Kristi L. Helke ◽  
Vanessa K. Hinson ◽  
...  

Biomedicines ◽  
2021 ◽  
Vol 9 (7) ◽  
pp. 789
Author(s):  
Ittetsu Kin ◽  
Tatsuya Sasaki ◽  
Takao Yasuhara ◽  
Masahiro Kameda ◽  
Takashi Agari ◽  
...  

Background: The major surgical treatment for Parkinson’s disease (PD) is deep brain stimulation (DBS), but a less invasive treatment is desired. Vagus nerve stimulation (VNS) is a relatively safe treatment without cerebral invasiveness. In this study, we developed a wireless controllable electrical stimulator to examine the efficacy of VNS on PD model rats. Methods: Adult female Sprague-Dawley rats underwent placement of a cuff-type electrode and stimulator on the vagus nerve. Following which, 6-hydroxydopamine (6-OHDA) was administered into the left striatum to prepare a PD model. VNS was started immediately after 6-OHDA administration and continued for 14 days. We evaluated the therapeutic effects of VNS with behavioral and immunohistochemical outcome assays under different stimulation intensity (0.1, 0.25, 0.5 and 1 mA). Results: VNS with 0.25–0.5 mA intensity remarkably improved behavioral impairment, preserved dopamine neurons, reduced inflammatory glial cells, and increased noradrenergic neurons. On the other hand, VNS with 0.1 mA and 1 mA intensity did not display significant therapeutic efficacy. Conclusions: VNS with 0.25–0.5 mA intensity has anti-inflammatory and neuroprotective effects on PD model rats induced by 6-OHDA administration. In addition, we were able to confirm the practicality and effectiveness of the new experimental device.


2017 ◽  
Vol 10 (6) ◽  
pp. 1045-1054 ◽  
Author(s):  
Ariana Q. Farrand ◽  
Kristi L. Helke ◽  
Rebecca A. Gregory ◽  
Monika Gooz ◽  
Vanessa K. Hinson ◽  
...  

2020 ◽  
Author(s):  
Supriyo Choudhury ◽  
Hrishikesh Kumar ◽  
Banashree Mondal

2019 ◽  
Vol 373 ◽  
pp. 112080 ◽  
Author(s):  
Ariana Q. Farrand ◽  
Kristi L. Helke ◽  
Luis Aponte-Cofresí ◽  
Monika B. Gooz ◽  
Rebecca A. Gregory ◽  
...  

2019 ◽  
Vol 34 (6) ◽  
pp. 918-919 ◽  
Author(s):  
Rosie Morris ◽  
Alison J. Yarnall ◽  
Heather Hunter ◽  
John‐Paul Taylor ◽  
Mark R. Baker ◽  
...  

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