Restoration of autophagic flux in myocardial tissues is required for cardioprotection of sevoflurane postconditioning in rats

Acta Pharmacologica Sinica

Volumn 35, Issue 6, 2014, Pages 758-769

  Zhang, Yu Lin ^a,b   Yao, Yun Tai ^a,b   Fang, Neng Xin ^a,b   Zhou, Cheng Hui ^a,b   Gong, Jun Song ^a,b   Li, Li Huan ^a,b  

^a PEKING UNION MEDICAL COLLEGE   (China)

^b FuWai Cardiovascular Hospital   (China)

Author keywords

autophagy; cardioprotection; chloroquine; heart; inhalation anesthetics; ischemia reperfusion injury; postconditioning; Sevoflurane

Indexed keywords

BECLIN 1; CATHEPSIN B; PROTEIN P62; SEVOFLURANE; TROPONIN I; CARDIOTONIC AGENT; ETHER DERIVATIVE; INHALATION ANESTHETIC AGENT;

ANIMAL EXPERIMENT; ANIMAL MODEL; APOPTOSIS; ARTICLE; AUTOPHAGOSOME; AUTOPHAGY; CELL VACUOLE; CONTROLLED STUDY; HEART INFARCTION SIZE; HEART MUSCLE ISCHEMIA; HEART PROTECTION; ISCHEMIC POSTCONDITIONING; ISCHEMIC PRECONDITIONING; MALE; NONHUMAN; RAT; REPERFUSION INJURY; ANIMAL; COMPLICATION; DRUG EFFECTS; HEART; HEART MUSCLE; MYOCARDIAL INFARCTION; MYOCARDIAL REPERFUSION INJURY; PATHOLOGY; SPRAGUE DAWLEY RAT;

ANESTHETICS, INHALATION; ANIMALS; AUTOPHAGY; CARDIOTONIC AGENTS; HEART; MALE; METHYL ETHERS; MYOCARDIAL INFARCTION; MYOCARDIAL REPERFUSION INJURY; MYOCARDIUM; RATS, SPRAGUE-DAWLEY;

EID: 84902264280     PISSN: 16714083     EISSN: 17457254     Source Type: Journal    
DOI: 10.1038/aps.2014.20     Document Type: Article

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