IndraLab

Statements



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"In cardiac cells exposed to ischemic conditions, in CME-induced excessive ROS generation, and in MI rats, rosuvastatin and LCZ696 were shown to effectively suppress ROS production and subsequently inhibit NLRP3-mediated pyroptosis43 53."

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"Similarly, rosuvastatin was found to reduce cardiac dysfunction in DCM rats by inhibiting NLRP3 inflammasomes [53]."

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"Furthermore, rosuvastatin significantly inhibited the activation of NLRP3 inflammasome in this animal model."

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"It has been showed that rosuvastatin and fenofibrate suppress the inflammatory process of cardiovascular disease by inhibiting NLRP3 inflammasome [6,31] ."

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"Rosuvastatin and other statins have been proven to attenuate inflammation and DCM via NLRP3 inflammasome and MAPK signaling pathways (57)."

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"This finding indicated that application of high dose of rosuvastatin could downregulate NLRP3 and its downstream effectors, thus alleviate inflammatory response in atherogenesis (Altaf et al., 2015)."

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"Both ticagrelor and rosuvastatin reduced postinfarction activation of NLRP3 inflammasome [136]."

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"Furthermore, spironolactone and rosuvastatin, the two-hit anti-inflammatory agents, reduced NLR family pyrin domain containing 3 (NLRP3)/GSDMD pyroptosis in EAT and autophagy in myocardium of HFpEF mouse."

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"Rosuvastatin and diosmetin inhibited the HSP70/TLR4 /NF-κB p65/NLRP3 signaling pathways and switched macrophage to M2 phenotype in a rat model of acute kidney injury induced by cisplatin."

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"Luo et al. 28 indicated that rosuvastatin, a type of anti-hyperlipidemic agent, inhibited the NLRP3 inflammasome via the MAPK pathway in DCM."