Journal
CHEMMEDCHEM
Volume 17, Issue 24, Pages -Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/cmdc.202200317
Keywords
Ischemic stroke; O-2 generation; Antithrombosis; Antioxidation; Neuroprotection
Categories
Funding
- National Natural Science Foundation of China [52061135202, 21807097, 51573186]
- National Key Research and Development Program of China [2018YFE0121400]
- Natural Science Foundation of Jilin Province of China [20190701030GH]
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In this study, nanodelivery systems based on MnO2 loaded with Ginkgolide B (GB) were designed to restore the intracerebral microenvironment in ischemic stroke. The study found that GB can protect brain tissue from oxidative damage by activating the Nrf2 signaling pathway. Meanwhile, MnO2 nanoparticles can penetrate the blood-brain barrier and enhance the delivery of therapeutic agents within brain tissue. This study provides a new therapeutic route for regulating the microenvironment of ischemic stroke.
Ischemic stroke is caused by cerebrovascular stenosis or occlusion. Excessive reactive oxygen species (ROS) are the focus-triggering factor of irreversible injury in ischemic regions, which result in harmful cascading effects to brain tissue, such as inflammation and microthrombus formation. In the present work, we designed nanodelivery systems (NDSs) based on MnO2 loaded with Ginkgolide B (GB) for restoring the intracerebral microenvironment in ischemic stroke, such as ROS scavenging, O-2 elevation, thrombus inhibition and damage repair. GB can activate the endogenous antioxidant defense of cells by enhancing the nuclear factor-E2-related factor 2 (Nrf2) signalling pathway, thus protecting brain tissue from oxidative damage. However, the blood-brain barrier (BBB) is also a therapeutic obstacle for the delivery of these agents to ischemic regions. MnO2 nanoparticles have an inherent BBB penetration effect, which enhances the delivery of therapeutic agents within brain tissue. MnO2, with mimicking enzymatic activity, can catalyze the decomposition of overproduced H2O2 in the ischemic microenvironment to O-2, meanwhile releasing platelet-antagonizing GB molecules, thus alleviating cerebral hypoxia, oxidative stress damage, and microthrombus generation. This study may provide a promising therapeutic route for regulating the microenvironment of ischemic stroke through a combined function of ROS scavenging, microthrombus inhibition, and BBB penetration.
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