Bioactive Ceria Nanoenzymes Target Mitochondria in Reperfusion Injury to Treat Ischemic Stroke.
Jun LiaoYi LiLi FanYuhan SunZhengyan GuQing-Qiang XuYun WangLiyan XiongKai XiaoZhe-Sheng ChenZhiwei MaChuan ZhangTingfang WangYing LuPublished in: ACS nano (2024)
Overproduction of reactive oxygen species by damaged mitochondria after ischemia is a key factor in the subsequent cascade of damage. Delivery of therapeutic agents to the mitochondria of damaged neurons in the brain is a potentially promising targeted therapeutic strategy for the treatment of ischemic stroke. In this study, we developed a ceria nanoenzymes synergistic drug-carrying nanosystem targeting mitochondria to address multiple factors of ischemic stroke. Each component of this nanosystem works individually as well as synergistically, resulting in a comprehensive therapy. Alleviation of oxidative stress and modulation of the mitochondrial microenvironment into a favorable state for ischemic tolerance are combined to restore the ischemic microenvironment by bridging mitochondrial and multiple injuries. This work also revealed the detailed mechanisms by which the proposed nanodelivery system protects the brain, which represents a paradigm shift in ischemic stroke treatment.
Keyphrases
- reactive oxygen species
- oxidative stress
- cerebral ischemia
- atrial fibrillation
- cell death
- cancer therapy
- stem cells
- ischemia reperfusion injury
- endoplasmic reticulum
- white matter
- dna damage
- resting state
- emergency department
- single cell
- blood brain barrier
- left ventricular
- combination therapy
- functional connectivity
- cell therapy
- percutaneous coronary intervention
- replacement therapy
- drug induced
- mesenchymal stem cells
- heat stress
- adverse drug
- smoking cessation