Affiliation:
1. Department of Neurosurgery, The First Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou, Zhejiang 310006, China
2. First Clinical Medical College, Zhejiang Chinese Medical University, Hangzhou, Zhejiang 310053, China
Abstract
Background:
Cerebral ischemia-reperfusion injury is caused by a blood reperfusion injury
in the ischemic brain and usually occurs in the treatment stage of ischemic disease, which can
aggravate brain tissue injury.
Objective:
Curcumin was reported to exert a good therapeutic effect on neural cells against ischemia-
reperfusion injury, However, the mechanism is not clear.
Methods:
In this study, Oxygen-Glucose Deprivation (OGD) model of fetal rat cerebral cortical
neurons and the Middle Cerebral Artery Occlusion (MCAO) model of rats were employed to mimic
cerebral ischemia-reperfusion injury in vitro and in vivo, respectively.
Results:
We confirmed that curcumin has a promotive effect on neuronal proliferation and an inhibitory
effect on neuronal pyroptosis. Furthermore, we found that curcumin could improve cerebral
infarction. The results of western blotting showed that curcumin down-regulated the expression
of nucleotide-binding oligomerization domain-containing protein-, leucine-rich repeats-, and
pyrin domain-containing protein 1 (NLRP1), cysteinyl aspartate-specific protease 1 (caspase-1),
gasdermin D (GSDMD), IL-1β, IL-6, TNF-α, and iNOS proteins in OGD and MCAO models. NLRP1-
dependent neuronal pyroptosis played an important role in cerebral ischemia-reperfusion
injury.
Conclusion:
Curcumin could effectively inhibit NLRP1-dependent neuronal pyroptosis by suppressing
the p38 MAPK pathway and therefore exerted neuroprotective effects against cerebral ischemia-
reperfusion injury.
Funder
National Natural Science Foundation of China
Publisher
Bentham Science Publishers Ltd.
Subject
Cellular and Molecular Neuroscience,Developmental Neuroscience,Neurology
Cited by
30 articles.
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