期刊
BIOMEDICINE & PHARMACOTHERAPY
卷 84, 期 -, 页码 1350-1358出版社
ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.biopha.2016.10.074
关键词
Dendrobium officinale; Diabetic cardiomyopathy; Oxidative stress; Lipid accumulation; Inflammation; Fibrosis
资金
- Chongqing Science and Technology Commission [cstc2016jcyjA0296]
- Fundamental Research Funds for the Central University [XDJK2014B024, XDJK2016E137]
- Innovative Project on Designing and Screening Drug Candidates of Chongqing [cstc2015zdcy-ztzx120003]
Dendrobium officinale Kimura et Migo (Dendrobium catenatum Lindley), a prized traditional Chinese Medicine, has been used in China and Southeast Asian countries for centuries. The present study was aimed to investigate the effects and the possible mechanisms of the Dendrobium officinale extracts (DOE) on diabetic cardiomyopathy in mice. The diabetic model was induced by intraperitoneal injection of streptozotocin at the dose of 50 mg/kg body weight for 5 consecutive days. After 8 weeks treatment of DOE, mice were sacrificed, blood sample and heart tissues were collected. Our results showed that Streptozotocin-induced diabetic model was effectively achieved and serum CK and LDH levels were significantly increased in mice with diabetic cardiomyopathy. Pretreatment with DOE decreased the heart-to-body weight ratio (HW/BW) and showed an evident hypoglycemic effect. DOE pretreatment significantly decreased CK, LDH, TC and TG levels, limited the production of MDA and increased the activities of T-SOD. The histological analysis of Oil red O staining and Sirius red staining showed an obvious amelioration of cardiac injury, inhibition of cardiac lipid accumulation and deposition of collagen when pretreatment with DOE. In addition, Western blot detection and analysis showed that DOE down-regulated the expression of TGF-beta, collegan-1, fibronectin, NF-kappa B, TNF-alpha and IL-1 beta. In conclusion, our study suggested that DOE possesses the cardioprotective potential against diabetic cardiomyopathy, which may be due to the inhibition of oxidative stress, cardiac lipid accumulation, pro-inflammatory cytokines and cardiac fibrosis. (C) 2016 Elsevier Masson SAS. All rights reserved.
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