Cyclosporine A loaded brain targeting nanoparticle to treat cerebral ischemia/reperfusion injury in mice
MPTP
Stroke
DOI:
10.1186/s12951-022-01474-x
Publication Date:
2022-06-03T10:03:45Z
AUTHORS (8)
ABSTRACT
Ischemic stroke is one of the main causes death and disability in world. The treatment for ischemic to restore blood perfusion as soon possible. However, when brain tissue re-perfused by blood, mitochondrial permeability transition pore (mPTP) neuron microglia excessively opened, resulting apoptosis nerve inflammation. This aggravates injury. Cyclosporine A (CsA) inhibits over-opening mPTP, subsequently reducing release ROS cerebral ischemia/reperfusion injured microglia. CsA insoluble water present high concentrations lymphatic tissue. Herein, infarction targeted nanoparticle (CsA@HFn) was developed treat injury.CsA@HFn efficiently penetrated blood-brain barrier (BBB) selectively accumulated area, inhibiting opening mPTP production neuron. reduced damage BBB. Consequently, CsA@HFn significantly infarct area. Moreover, inhibited recruitment astrocytes region polarized into M2 type microglia, which alleviated inflammation.CsA@HFn showed a significant therapeutic effect on injury alleviating neuron, inflammation BBB has great potential stroke.
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