TY - GEN
T1 - Neuromodulation therapies and potential treatments for traumatic brain injury
AU - Zhang, Zhining
PY - 2022
Y1 - 2022
N2 - Traumatic brain injury (TBI) is a leading cause of death and disability throughout the world. Its primary and secondary damage can lead to impaired neurological function and serious complications such as post-traumatic stress disorder, cognitive or behavioural impairment, epilepsy and neurodegenerative diseases.This article outlines the main mechanisms of secondary brain injury and provides an updated direction for potential neuroprotective treatments. Among other things, current clinical studies suggest that vagus nerve stimulation (VNS) may reduce brain injury after TBI by inhibiting oxidative stress, inflammation and apoptosis, promote recovery of consciousness and cognitive function after experimental TBI, enhance motor and cognitive recovery, reduce brain oedema and inflammation, reduce blood-brain barrier disruption, and confer neuroprotection. In addition, the literature describes deep brain stimulation, gene therapy targeting the combined regeneration of stem cells and biomaterials for TB repair, novel neuroprotective drugs and nanomaterials enabling electrophysiological recording tests and biochemical modulation. Although the data suggest that these potential therapeutic approaches are beneficial for the eventual outcome of TBI, their availability for good use in clinical trials needs to be further explored.
AB - Traumatic brain injury (TBI) is a leading cause of death and disability throughout the world. Its primary and secondary damage can lead to impaired neurological function and serious complications such as post-traumatic stress disorder, cognitive or behavioural impairment, epilepsy and neurodegenerative diseases.This article outlines the main mechanisms of secondary brain injury and provides an updated direction for potential neuroprotective treatments. Among other things, current clinical studies suggest that vagus nerve stimulation (VNS) may reduce brain injury after TBI by inhibiting oxidative stress, inflammation and apoptosis, promote recovery of consciousness and cognitive function after experimental TBI, enhance motor and cognitive recovery, reduce brain oedema and inflammation, reduce blood-brain barrier disruption, and confer neuroprotection. In addition, the literature describes deep brain stimulation, gene therapy targeting the combined regeneration of stem cells and biomaterials for TB repair, novel neuroprotective drugs and nanomaterials enabling electrophysiological recording tests and biochemical modulation. Although the data suggest that these potential therapeutic approaches are beneficial for the eventual outcome of TBI, their availability for good use in clinical trials needs to be further explored.
KW - Deep brain stimulation
KW - nanomaterials
KW - Neuroprotective drugs
KW - Traumatic brain injury
KW - Vagal nerve stimulation
UR - http://www.scopus.com/inward/record.url?scp=85145020212&partnerID=8YFLogxK
U2 - 10.1117/12.2660149
DO - 10.1117/12.2660149
M3 - Conference paper
AN - SCOPUS:85145020212
T3 - Proceedings of SPIE - The International Society for Optical Engineering
BT - International Conference on Biomedical and Intelligent Systems, IC-BIS 2022
A2 - El-Hashash, Ahmed
PB - SPIE-SOC PHOTO-OPTICAL INSTRUMENTATION ENGINEERS
T2 - 2022 International Conference on Biomedical and Intelligent Systems, IC-BIS 2022
Y2 - 24 June 2022 through 26 June 2022
ER -