Journal
PHYTOMEDICINE
Volume 94, Issue -, Pages -Publisher
ELSEVIER GMBH
DOI: 10.1016/j.phymed.2021.153849
Keywords
Protocatechuic aldehyde; Ischemic injury; lncRNA Xist; Pyroptosis; rBMEC
Categories
Funding
- National Key Research and Devel-opment Project [2019YFC1708600, 2019YFC1708604]
- National Natural Science Foundation of China [81803992, 81874366, 81630105]
- Natural Science Foundation of Zhejiang Province, China [LZ17H270001]
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The study demonstrated that PCA effectively attenuates BMEC pyroptosis under ischemic injury by enhancing antioxidant activity, regulating protein expression, reducing cerebral infarct volume in MCAO rats, and promoting cell survival in rBMECs. The crucial role of lncRNA Xist in mediating the anti-pyroptosis effects of PCA on rBMECs was also highlighted in this research.
Background: Pyroptosis is a pro-inflammatory cell death characterized by the formation of inflammasomes. Abnormal inflammation in brain microvascular endothelial cells (BMECs) has been correlated with ischemic stroke. Protocatechuic aldehyde (PCA) is a hydrophilic phenolic acid derived from the traditional Chinese herb Salvia miltiorrhiza with significant anti-inflammatory effects. However, the mechanism of PCA on BMEC pyroptosis under ischemic injury has been largely unexplored. Purpose: We aimed to study the effects and mechanism of PCA on BMEC pyroptosis under ischemic injury. Methods: Sprague-Dawley (SD) rats were injected through the tail vein with different concentrations of PCA after transient middle cerebral artery occlusion (MCAO) was performed. The protective effects of PCA in SD rats were examined via neurological scores, infarct volume evaluation, and anti-pyroptosis effects using immunofluorescence staining and western blot. Rat BMECs (rBMECs) were treated with different concentrations of PCA after oxygen and glucose deprivation (OGD). The ability of PCA to protect rBMECs was examined via cell viability, anti-oxidative activity, and anti-pyroptosis effects as determined by qRT-PCR and western blot. Additionally, the role of lncRNA Xist in anti-pyroptosis responses of PCA-treated rBMECs was validated with lncRNA Xist siRNA. Results: We found that treatment with MCAO and OGD increased the expression of NOD-like receptor protein 3, gasdermin D, Caspase-1, interleukin-1 beta, and NIMA-related kinase 7, which was reversed by treatment with PCA or MCC950 (a pyroptosis inhibitor). In addition, PCA reduced the cerebral infarct volume in MCAO rats and promoted cell survival and proliferation in OGD/reperfusion-treated rBMECs. PCA enhanced the antioxidant activity and mitochondrial membrane potential in rBMECs. PCA also enhanced lncRNA Xist expression, and when the expression of lncRNA Xist was silenced, PCA could not alleviate pyroptosis well in rBMECs. Conclusion: Protocatechuic aldehyde prevents ischemic injury by attenuating rBMEC pyroptosis via lncRNA Xist.
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