Nanotherapeutic modulation of excitotoxicity and oxidative stress in acute brain injury.
Rick LiaoThomas R WoodElizabeth NancePublished in: Nanobiomedicine (2020)
Excitotoxicity is a primary pathological process that occurs during stroke, traumatic brain injury (TBI), and global brain ischemia such as perinatal asphyxia. Excitotoxicity is triggered by an overabundance of excitatory neurotransmitters within the synapse, causing a detrimental cascade of excessive sodium and calcium influx, generation of reactive oxygen species, mitochondrial damage, and ultimately cell death. There are multiple potential points of intervention to combat excitotoxicity and downstream oxidative stress, yet there are currently no therapeutics clinically approved for this specific purpose. For a therapeutic to be effective against excitotoxicity, the therapeutic must accumulate at the disease site at the appropriate concentration at the right time. Nanotechnology can provide benefits for therapeutic delivery, including overcoming physiological obstacles such as the blood-brain barrier, protect cargo from degradation, and provide controlled release of a drug. This review evaluates the use of nano-based therapeutics to combat excitotoxicity in stroke, TBI, and hypoxia-ischemia with an emphasis on mitigating oxidative stress, and consideration of the path forward toward clinical translation.
Keyphrases
- oxidative stress
- traumatic brain injury
- brain injury
- cell death
- cerebral ischemia
- diabetic rats
- dna damage
- subarachnoid hemorrhage
- ischemia reperfusion injury
- reactive oxygen species
- atrial fibrillation
- induced apoptosis
- randomized controlled trial
- liver failure
- pregnant women
- small molecule
- severe traumatic brain injury
- human health
- multiple sclerosis
- heat shock
- physical activity
- respiratory failure
- acute respiratory distress syndrome
- weight loss
- extracorporeal membrane oxygenation
- cell proliferation
- drug administration