Diabetes blocks the cardioprotective effects of sevoflurane postconditioning by impairing Nrf2/Brg1/HO-1 signaling

European Journal of Pharmacology

Volumn 779, Issue , 2016, Pages 111-121

  Gao, Sumin ^a   Yang, Zhengchao ^a   Shi, Ruili ^a   Xu, Dan ^a   Li, Haobo ^b   Xia, Zhengyuan ^b   Wu, Qing Ping ^a   Yao, Shanglong ^a   Wang, Tingting ^a   Yuan, Shiying ^a  

^a HUAZHONG UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

^b UNIVERSITY OF HONG KONG   (Hong Kong)

Author keywords

Brg1; Diabetes; HO 1; Nrf2; Postconditioning; Sevoflurane

Indexed keywords

BRG1 PROTEIN; GLUCOSE; HEME OXYGENASE 1; PROTOPORPHYRIN ZINC; SEVOFLURANE; STREPTOZOCIN; TRANSCRIPTION FACTOR NRF2; CARDIOTONIC AGENT; DNA HELICASE; ETHER DERIVATIVE; MALONALDEHYDE; NUCLEAR PROTEIN; SMARCA4 PROTEIN, MOUSE; SUPEROXIDE; SUPEROXIDE DISMUTASE; TRANSCRIPTION FACTOR;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; APOPTOSIS; ARTICLE; CONTROLLED STUDY; CORONARY ARTERY OCCLUSION; DIABETES MELLITUS; DRUG EFFECT; ENZYME INHIBITION; HEART INFARCTION SIZE; HEART MUSCLE CELL; HEART MUSCLE ISCHEMIA; HEART PROTECTION; IN VITRO STUDY; IN VIVO STUDY; ISCHEMIC POSTCONDITIONING; MALE; MOUSE; NONHUMAN; OXIDATIVE STRESS; PRIORITY JOURNAL; PROTEIN EXPRESSION; REPERFUSION INJURY; SIGNAL TRANSDUCTION; STREPTOZOTOCIN-INDUCED DIABETES MELLITUS; ANIMAL; CARDIAC MUSCLE CELL; CELL LINE; COMPLICATION; DRUG EFFECTS; EXPERIMENTAL DIABETES MELLITUS; METABOLISM; PATHOLOGY; PATHOPHYSIOLOGY;

ANIMALS; APOPTOSIS; CARDIOTONIC AGENTS; CELL LINE; DIABETES MELLITUS, EXPERIMENTAL; DNA HELICASES; HEME OXYGENASE-1; ISCHEMIC POSTCONDITIONING; MALE; MALONDIALDEHYDE; METHYL ETHERS; MICE; MYOCARDIAL ISCHEMIA; MYOCYTES, CARDIAC; NF-E2-RELATED FACTOR 2; NUCLEAR PROTEINS; SIGNAL TRANSDUCTION; SUPEROXIDE DISMUTASE; SUPEROXIDES; TRANSCRIPTION FACTORS;

EID: 84961190006     PISSN: 00142999     EISSN: 18790712     Source Type: Journal    
DOI: 10.1016/j.ejphar.2016.03.018     Document Type: Article

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