Recovery of Function after Vagus Nerve Stimulation Initiated 24 Hours after Fluid Percussion Brain Injury

2006 ◽  
Vol 23 (10) ◽  
pp. 1549-1560 ◽  
Author(s):  
Douglas C. Smith ◽  
Arlene A. Tan ◽  
Andrea Duke ◽  
Steven L. Neese ◽  
Richard W. Clough ◽  
...  
2016 ◽  
Vol 33 (9) ◽  
pp. 871-879 ◽  
Author(s):  
David T. Pruitt ◽  
Ariel N. Schmid ◽  
Lily J. Kim ◽  
Caroline M. Abe ◽  
Jenny L. Trieu ◽  
...  

Neuroscience ◽  
2007 ◽  
Vol 147 (2) ◽  
pp. 286-293 ◽  
Author(s):  
R.W. Clough ◽  
S.L. Neese ◽  
L.K. Sherill ◽  
A.A. Tan ◽  
A. Duke ◽  
...  

2014 ◽  
Vol 9 (17) ◽  
pp. 1585 ◽  
Author(s):  
Yigang Yu ◽  
Long Zhou ◽  
Jinhuang Lin ◽  
Junming Lin ◽  
Guoju Kui ◽  
...  

Stroke ◽  
2015 ◽  
Vol 46 (suppl_1) ◽  
Author(s):  
Navid Khodaparast ◽  
Reema Casavant ◽  
Andrea Ruiz ◽  
Robert L Rennaker ◽  
Michael P Kilgard

Background: Stroke is the leading cause of serious long-term disability. Currently, there is no effective treatment for chronic stroke patients. Neuroplasticity within motor circuitry is believed to support recovery of function after stroke. We have developed a method using vagus nerve stimulation (VNS) paired with motor training to drive robust, specific plasticity in the motor cortex. Our recent studies indicated that VNS paired with rehab training significantly enhances recovery of forelimb function after cortical ischemic stroke. To further the translation potential of our therapy, we accessed the hypothesis that delivering VNS paired with rehab may improve functional recovery in rats that demonstrated chronic forelimb impairments. Methods: All female Sprague Dawley rats were trained on the Isometric Pull Task, which quantifiably measures forelimb force generation. Rats that achieved 5 consecutive days of over 85% hit rate on this task were given a unilateral cortical-subcortical ischemic lesion via injections of a vasoconstrictive peptide, endothelin-1. Following the lesion, rats returned to their home cage, and did not begin rehab training until 5 weeks post-lesion. Upon return, post-lesion forelimb impairment was accessed with the same task parameters used during pre-lesion training, which allowed for a direct comparison of performance. Rats were assigned to balanced treatment groups based on post-lesion baseline hit rate. Treatment groups consisted of VNS delivered during rehab training (Paired VNS; n=10), VNS delivered two hours after rehab training (Delayed VNS; n=10), and rehab training without VNS (Rehab; n=10). Results: At five weeks post-lesion, the unilateral ischemic insult significantly worsened performance in all three groups compared to pre-lesion (Paired VNS: 29.8 ± 5.7%, paired t-test, P < 0.001; Delayed VNS: 24.6 ± 2.7%, P < 0.001; Rehab: 30.4 ± 4.7%, P < 0.001). Following our therapy, the Paired VNS group demonstrated significantly better performance than both control groups (Paired VNS: 81.6 ± 2.3%, P < 0.01; Delayed VNS: 53.2 ± 6.5%, P < 0.01; Rehab: 49.8 ± 6.8%, P < 0.01). Conclusion: Our results indicate that VNS paired with rehab training can further enhance recovery of forelimb function in chronically impaired rats.


2015 ◽  
Vol 24 (2) ◽  
pp. 308-319 ◽  
Author(s):  
Daniel Neren ◽  
Matthew D. Johnson ◽  
Wynn Legon ◽  
Salam P. Bachour ◽  
Geoffrey Ling ◽  
...  

2020 ◽  
Vol 34 (9) ◽  
pp. 831-843
Author(s):  
Yunliang Tang ◽  
Xiaoyang Dong ◽  
Gengfa Chen ◽  
Wen Ye ◽  
Junwei Kang ◽  
...  

Background Traumatic brain injury (TBI) is a major cause of death and disability worldwide. Oxidative stress, inflammation, and apoptosis are vital pathophysiological features post-TBI. Objectives Research has shown that vagus nerve stimulation (VNS) can attenuate oxidative stress in various diseases. However, the critical role of VNS in TBI is still not completely understood. This study investigated the protective effects and potential mechanism of VNS on TBI. Methods Male Sprague-Dawley rats were randomized into 3 groups: sham, TBI, and TBI + VNS. The TBI model was induced in rats by the free-fall drop method. The vagal nerve trunk was separated, and VNS was performed after establishing the TBI model. Results The results showed that VNS significantly ameliorated tissue damage, neurological deficits, and cerebral edema, compared with the sham VNS group. Additionally, VNS alleviated oxidative stress, inflammation, and apoptosis in the pericontusive cortex of rats after TBI. VNS also significantly suppressed expression of the nuclear factor-κB (NF-κB) protein in the nucleus and activation of the nucleotide-binding domain–like receptor protein 3 (NLRP3) inflammasome. Conclusions Taken together, the present study indicates that VNS may attenuate brain damage after TBI by inhibiting oxidative stress, inflammation, and apoptosis, possibly through the NF-κB/NLRP3 signaling pathway.


2019 ◽  
Vol 12 (2) ◽  
pp. 418-419
Author(s):  
A. Schindler ◽  
J. Meabon ◽  
B. Baskin ◽  
E. Cooper ◽  
M. Yagi ◽  
...  

2007 ◽  
Vol 1128 ◽  
pp. 157-163 ◽  
Author(s):  
Steven L. Neese ◽  
Luke K. Sherill ◽  
Arlene A. Tan ◽  
Rodney W. Roosevelt ◽  
Ronald A. Browning ◽  
...  

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