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http://purl.uniprot.org/citations/26964694http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/26964694http://www.w3.org/2000/01/rdf-schema#comment"Positive evidence from clinical trials has fueled growing acceptance of traditional Chinese medicine (TCM) for the treatment of cardiac diseases; however, little is known about the underlying mechanisms. Here, we investigated the nature and underlying mechanisms of the effects of YiXin-Shu (YXS), an antioxidant-enriched TCM formula, on myocardial ischemia/reperfusion (MI/R) injury. YXS pretreatment significantly reduced infarct size and improved viable myocardium metabolism and cardiac function in hypercholesterolemic mice. Mechanistically, YXS attenuated myocardial apoptosis by inhibiting the mitochondrial mediated apoptosis pathway (as reflected by inhibition of mitochondrial swelling, cytochrome c release and caspase-9 activity, and normalization of Bcl-2 and Bax levels) without altering the death receptor and endoplasmic reticulum-stress death pathways. Moreover, YXS reduced oxidative/nitrative stress (as reflected by decreased superoxide and nitrotyrosine content and normalized pro- and anti-oxidant enzyme levels). Interestingly, YXS upregulated endogenous nuclear receptors including LXRα, PPARα, PPARβ and ERα, and in-vivo knockdown of cardiac-specific LXRα significantly blunted the cardio-protective effects of YXS. Collectively, these data show that YXS is effective in mitigating MI/R injury by suppressing mitochondrial mediated apoptosis and oxidative stress and by upregulating LXRα, thereby providing a rationale for future clinical trials and clinical applications."xsd:string
http://purl.uniprot.org/citations/26964694http://purl.org/dc/terms/identifier"doi:10.1038/srep23025"xsd:string
http://purl.uniprot.org/citations/26964694http://purl.uniprot.org/core/author"He B."xsd:string
http://purl.uniprot.org/citations/26964694http://purl.uniprot.org/core/author"Gao L."xsd:string
http://purl.uniprot.org/citations/26964694http://purl.uniprot.org/core/author"Qiao Z."xsd:string
http://purl.uniprot.org/citations/26964694http://purl.uniprot.org/core/author"Xu L."xsd:string
http://purl.uniprot.org/citations/26964694http://purl.uniprot.org/core/author"Su Y."xsd:string
http://purl.uniprot.org/citations/26964694http://purl.uniprot.org/core/author"Zhao Y."xsd:string
http://purl.uniprot.org/citations/26964694http://purl.uniprot.org/core/author"Pu J."xsd:string
http://purl.uniprot.org/citations/26964694http://purl.uniprot.org/core/author"Ding S."xsd:string
http://purl.uniprot.org/citations/26964694http://purl.uniprot.org/core/author"Ying X."xsd:string
http://purl.uniprot.org/citations/26964694http://purl.uniprot.org/core/author"Lin N."xsd:string
http://purl.uniprot.org/citations/26964694http://purl.uniprot.org/core/date"2016"xsd:gYear
http://purl.uniprot.org/citations/26964694http://purl.uniprot.org/core/name"Sci Rep"xsd:string
http://purl.uniprot.org/citations/26964694http://purl.uniprot.org/core/pages"23025"xsd:string
http://purl.uniprot.org/citations/26964694http://purl.uniprot.org/core/title"YiXin-Shu, a ShengMai-San-based traditional Chinese medicine formula, attenuates myocardial ischemia/reperfusion injury by suppressing mitochondrial mediated apoptosis and upregulating liver-X-receptor alpha."xsd:string
http://purl.uniprot.org/citations/26964694http://purl.uniprot.org/core/volume"6"xsd:string
http://purl.uniprot.org/citations/26964694http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/26964694
http://purl.uniprot.org/citations/26964694http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/26964694
http://purl.uniprot.org/uniprot/#_B2R8B9-mappedCitation-26964694http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/26964694
http://purl.uniprot.org/uniprot/#_B6ZGS8-mappedCitation-26964694http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/26964694
http://purl.uniprot.org/uniprot/#_B3KV37-mappedCitation-26964694http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/26964694
http://purl.uniprot.org/uniprot/#_B4DXU5-mappedCitation-26964694http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/26964694
http://purl.uniprot.org/uniprot/#_B5MBY7-mappedCitation-26964694http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/26964694