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表没食子儿茶素没食子酸酯通过限制线粒体DNA(mtDNA)释放减轻髋部骨折诱导的急性肺损伤。

Epigallocatechin Gallate Attenuates Hip Fracture-Induced Acute Lung Injury by Limiting Mitochondrial DNA (mtDNA) Release.

作者信息

Zhao Xiao-Dan, Liu Hao, Li Tao, Gong Quan, Zhang Wen-Li

机构信息

Department of Orthopedics, West China Hospital of Sichuan University, Chengdu, Sichuan, China (mainland).

出版信息

Med Sci Monit. 2017 Jul 12;23:3367-3372. doi: 10.12659/msm.902477.

DOI:10.12659/msm.902477
PMID:28698540
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5519220/
Abstract

BACKGROUND To study the protective effects and explore the mechanism of epigallocatechingallate (EGCG) on the hip fracture-induced acute lung injury. MATERIAL AND METHODS Thirty male Sprague-Dawley (SD) rats were randomly divided into the control group, hip fracture group, and hip fracture + EGCG (10 mg/Kg) group. After 24 h, blood samples, bronchoalveolar lavage fluid (BALF), and lung tissue were collected. Serum mitochondrial DNA (mtDNA) was measured by RT-PCR and BALF was used to perform cytological analysis and enzyme-linked immunosorbent assay (ELISA) assay. Lung tissue was used to evaluate the injury level. RESULTS EGCG significantly reduced the hip fracture-induced high level of serum mtDNA (p<0.05). HE staining showed protective effects of EGCG. Lower lung injury score and wet/dry ratio were identified in the hip fracture + EGCG group than in the hip fracture group (p<0.05). We found significantly lower levels of infiltration of inflammatory cells and production of inflammatory cytokines in the BALF of the hip fracture + EGCG group than in the hip fracture group (p<0.05). CONCLUSIONS Our study found that EGCG had protective effects on hip fracture-induced acute lung injury and suggests that EGCG exerts its protective effects through limiting the release of mtDNA. Our results provide a novel pharmacological agent to attenuate hip fracture-induced acute lung injury, as well as a potential theory to better explain the anti-inflammatory property of EGCG.

摘要

背景 研究表没食子儿茶素没食子酸酯(EGCG)对髋部骨折所致急性肺损伤的保护作用并探讨其机制。材料与方法 将30只雄性Sprague-Dawley(SD)大鼠随机分为对照组、髋部骨折组和髋部骨折+EGCG(10mg/Kg)组。24小时后,采集血样、支气管肺泡灌洗液(BALF)和肺组织。通过RT-PCR检测血清线粒体DNA(mtDNA),并使用BALF进行细胞学分析和酶联免疫吸附测定(ELISA)。肺组织用于评估损伤程度。结果 EGCG显著降低了髋部骨折所致的血清mtDNA高水平(p<0.05)。HE染色显示EGCG具有保护作用。与髋部骨折组相比,髋部骨折+EGCG组的肺损伤评分和湿/干比更低(p<0.05)。我们发现,与髋部骨折组相比,髋部骨折+EGCG组BALF中的炎症细胞浸润水平和炎症细胞因子产生水平显著更低(p<0.05)。结论 我们的研究发现EGCG对髋部骨折所致急性肺损伤具有保护作用,并表明EGCG通过限制mtDNA的释放发挥其保护作用。我们的结果提供了一种减轻髋部骨折所致急性肺损伤的新型药物,以及一种更好地解释EGCG抗炎特性的潜在理论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d1f/5519220/4d8c924ae573/medscimonit-23-3367-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d1f/5519220/aae6231cbb18/medscimonit-23-3367-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d1f/5519220/e04764423bf9/medscimonit-23-3367-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d1f/5519220/4e8b714372c6/medscimonit-23-3367-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d1f/5519220/4d8c924ae573/medscimonit-23-3367-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d1f/5519220/aae6231cbb18/medscimonit-23-3367-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d1f/5519220/e04764423bf9/medscimonit-23-3367-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d1f/5519220/4e8b714372c6/medscimonit-23-3367-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d1f/5519220/4d8c924ae573/medscimonit-23-3367-g004.jpg

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