Nanozymes: Potential Therapies for Reactive Oxygen Species Overproduction and Inflammation in Ischemic Stroke and Traumatic Brain Injury.
Yunfan YangZixiang LiXiaochong FanChao JiangJunmin WangYousef Rastegar-KashkooliTom J WangJunyang WangMenglu WangNannan ChengXiqian YuanXuemei ChenBing JiangJian WangPublished in: ACS nano (2024)
Nanozymes, which can selectively scavenge reactive oxygen species (ROS), have recently emerged as promising candidates for treating ischemic stroke and traumatic brain injury (TBI) in preclinical models. ROS overproduction during the early phase of these diseases leads to oxidative brain damage, which has been a major cause of mortality worldwide. However, the clinical application of ROS-scavenging enzymes is limited by their short in vivo half-life and inability to cross the blood-brain barrier. Nanozymes, which mimic the catalytic function of natural enzymes, have several advantages, including cost-effectiveness, high stability, and easy storage. These advantages render them superior to natural enzymes for disease diagnosis and therapeutic interventions. This review highlights recent advancements in nanozyme applications for ischemic stroke and TBI, emphasizing their potential to mitigate the detrimental effect of ROS overproduction, oxidative brain damage, inflammation, and blood-brain barrier compromise. Therefore, nanozymes represent a promising treatment modality for ROS overproduction conditions in future medical practices.
Keyphrases
- reactive oxygen species
- traumatic brain injury
- blood brain barrier
- oxidative stress
- dna damage
- cell death
- cerebral ischemia
- atrial fibrillation
- healthcare
- severe traumatic brain injury
- primary care
- white matter
- cardiovascular events
- physical activity
- risk factors
- stem cells
- resting state
- coronary artery disease
- multiple sclerosis
- cell therapy
- mesenchymal stem cells
- risk assessment
- combination therapy
- climate change
- crystal structure