<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>23(1)</volume><submitter>Cheng XF</submitter><pubmed_abstract>&lt;h4>Background/aims&lt;/h4>The activation of the complement system and subsequent inflammatory responses are important features of myocardial ischemia/reperfusion (I/R) injury. Exosomes are nanoscale extracellular vesicles that play a significant role in remote ischemic preconditioning (RIPC) cardioprotection. The present study aimed to test whether RIPC-induced plasma exosomes (RIPC-Exo) exert protective effects on myocardial I/R injury by inhibiting complement activation and inflammation and whether exosomal heat shock protein 90 (HSP90) mediates these effects.&lt;h4>Methods&lt;/h4>Rat hearts underwent 30 min of coronary ligation followed by 2 h of reperfusion. Plasma exosomes were isolated from RIPC rats and injected into the infarcted myocardium immediately after ligation. Sixty rats were rando</pubmed_abstract><journal>BMC cardiovascular disorders</journal><pagination>58</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9890892</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Exosomal HSP90 induced by remote ischemic preconditioning alleviates myocardial ischemia/reperfusion injury by inhibiting complement activation and inflammation.</pubmed_title><pmcid>PMC9890892</pmcid><pubmed_authors>Wang M</pubmed_authors><pubmed_authors>Tu RH</pubmed_authors><pubmed_authors>He ST</pubmed_authors><pubmed_authors>Bi Q</pubmed_authors><pubmed_authors>Cheng XF</pubmed_authors><pubmed_authors>Zhong GQ</pubmed_authors><pubmed_authors>Meng JJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Exosomal HSP90 induced by remote ischemic preconditioning alleviates myocardial ischemia/reperfusion injury by inhibiting complement activation and inflammation.</name><description>&lt;h4>Background/aims&lt;/h4>The activation of the complement system and subsequent inflammatory responses are important features of myocardial ischemia/reperfusion (I/R) injury. Exosomes are nanoscale extracellular vesicles that play a significant role in remote ischemic preconditioning (RIPC) cardioprotection. The present study aimed to test whether RIPC-induced plasma exosomes (RIPC-Exo) exert protective effects on myocardial I/R injury by inhibiting complement activation and inflammation and whether exosomal heat shock protein 90 (HSP90) mediates these effects.&lt;h4>Methods&lt;/h4>Rat hearts underwent 30 min of coronary ligation followed by 2 h of reperfusion. Plasma exosomes were isolated from RIPC rats and injected into the infarcted myocardium immediately after ligation. Sixty rats were rando</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Feb</publication><modification>2026-07-16T21:13:21.321Z</modification><creation>2025-04-05T20:52:34.972Z</creation></dates><accession>S-EPMC9890892</accession><cross_references><pubmed>36726083</pubmed><doi>10.1186/s12872-023-03043-y</doi></cross_references></HashMap>