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木兰提取物(BL153)对心脏的保护作用可防止高脂饮食喂养小鼠出现脂质积累、心脏氧化损伤、炎症及细胞死亡。

Magnolia extract (BL153) protection of heart from lipid accumulation caused cardiac oxidative damage, inflammation, and cell death in high-fat diet fed mice.

作者信息

Sun Weixia, Zhang Zhiguo, Chen Qiang, Yin Xia, Fu Yaowen, Zheng Yang, Cai Lu, Kim Ki-Soo, Kim Ki Ho, Tan Yi, Kim Young Heui

机构信息

Departments of Nephrology and Cardiology, The First Hospital of Jilin University, Changchun 130021, China ; Kosair Children's Hospital Research Institute, Department of Pediatrics, University of Louisville, Louisville, KY 40202, USA.

Kosair Children's Hospital Research Institute, Department of Pediatrics, University of Louisville, Louisville, KY 40202, USA ; Preventive Medicine School, Jilin University, Changchun 130021, China.

出版信息

Oxid Med Cell Longev. 2014;2014:205849. doi: 10.1155/2014/205849. Epub 2014 Feb 16.

Abstract

Magnolia as an herbal material obtained from Magnolia officinalis has been found to play an important role in anti-inflammation, antioxidative stress, and antiapoptosis. This study was designed to investigate the effect of Magnolia extract (BL153) on obesity-associated lipid accumulation, inflammation, oxidative stress, and apoptosis in the heart. C57BL/6 mice were fed a low- (10 kcal% fat) or high-fat (60 kcal% fat) diet for 24 weeks to induce obesity. These mice fed with high-fat diet (HFD) were given a gavage of vehicle, 2.5, 5, or 10 mg/kg body weight BL153 daily. The three doses of BL153 treatment slightly ameliorated insulin resistance without decrease of body weight gain induced by HFD feeding. BL153 at 10 mg/kg slightly attenuated a mild cardiac hypertrophy and dysfunction induced by HFD feeding. Both 5 mg/kg and 10 mg/kg of BL153 treatment significantly inhibited cardiac lipid accumulation measured by Oil Red O staining and improved cardiac inflammation and oxidative stress by downregulating ICAM-1, TNF-α, PAI-1, 3-NT, and 4-HNE. TUNEL staining showed that BL153 treatment also ameliorated apoptosis induced by mitochondrial caspase-3 independent cell death pathway. This study demonstrates that BL153 attenuates HFD-associated cardiac damage through prevention of HFD-induced cardiac lipid accumulation, inflammation, oxidative stress, and apoptosis.

摘要

厚朴作为一种从厚朴中提取的草药材料,已被发现具有抗炎、抗氧化应激和抗凋亡的重要作用。本研究旨在探讨厚朴提取物(BL153)对肥胖相关的心脏脂质积累、炎症、氧化应激和凋亡的影响。将C57BL/6小鼠分别喂食低脂肪(10千卡%脂肪)或高脂肪(60千卡%脂肪)饮食24周以诱导肥胖。给这些喂食高脂肪饮食(HFD)的小鼠每天灌胃给予载体、2.5、5或10毫克/千克体重的BL153。三种剂量的BL153治疗轻微改善了胰岛素抵抗,但并未降低HFD喂养引起的体重增加。10毫克/千克的BL153略微减轻了HFD喂养引起的轻度心脏肥大和功能障碍。5毫克/千克和10毫克/千克的BL153治疗均通过下调ICAM-1、TNF-α、PAI-1、3-NT和4-HNE,显著抑制了用油红O染色测定的心脏脂质积累,并改善了心脏炎症和氧化应激。TUNEL染色显示,BL153治疗还改善了由线粒体半胱天冬酶-3非依赖性细胞死亡途径诱导的凋亡。本研究表明,BL153通过预防HFD诱导的心脏脂质积累、炎症、氧化应激和凋亡,减轻了HFD相关的心脏损伤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32df/3945234/fed857064e0e/OMCL2014-205849.001.jpg

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