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本文引用的文献

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Phloretin attenuates LPS-induced acute lung injury in mice via modulation of the NF-κB and MAPK pathways.根皮素通过调节NF-κB和MAPK信号通路减轻脂多糖诱导的小鼠急性肺损伤。
Int Immunopharmacol. 2016 Nov;40:98-105. doi: 10.1016/j.intimp.2016.08.035. Epub 2016 Aug 30.
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Receptor Interacting Protein 3-Mediated Necroptosis Promotes Lipopolysaccharide-Induced Inflammation and Acute Respiratory Distress Syndrome in Mice.受体相互作用蛋白3介导的坏死性凋亡促进小鼠脂多糖诱导的炎症和急性呼吸窘迫综合征
PLoS One. 2016 May 19;11(5):e0155723. doi: 10.1371/journal.pone.0155723. eCollection 2016.
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Matrine Attenuates COX-2 and ICAM-1 Expressions in Human Lung Epithelial Cells and Prevents Acute Lung Injury in LPS-Induced Mice.苦参碱减轻人肺上皮细胞中COX-2和ICAM-1的表达并预防脂多糖诱导的小鼠急性肺损伤。
Mediators Inflamm. 2016;2016:3630485. doi: 10.1155/2016/3630485. Epub 2016 Jan 5.
4
The Protective Effects of HJB-1, a Derivative of 17-Hydroxy-Jolkinolide B, on LPS-Induced Acute Distress Respiratory Syndrome Mice.17-羟基乔松素内酯B衍生物HJB-1对脂多糖诱导的急性呼吸窘迫综合征小鼠的保护作用
Molecules. 2016 Jan 11;21(1):77. doi: 10.3390/molecules21010077.
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Early Treatment of Severe Acute Respiratory Distress Syndrome.重症急性呼吸窘迫综合征的早期治疗
Emerg Med Clin North Am. 2016 Feb;34(1):1-14. doi: 10.1016/j.emc.2015.08.001. Epub 2015 Nov 3.
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The role of inhaled prostacyclin in treating acute respiratory distress syndrome.吸入性前列环素在治疗急性呼吸窘迫综合征中的作用。
Ther Adv Respir Dis. 2015 Dec;9(6):302-12. doi: 10.1177/1753465815599345. Epub 2015 Aug 20.
7
Emerging therapies for the prevention of acute respiratory distress syndrome.预防急性呼吸窘迫综合征的新兴疗法。
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Usnic acid protects LPS-induced acute lung injury in mice through attenuating inflammatory responses and oxidative stress.松萝酸通过减轻炎症反应和氧化应激来保护脂多糖诱导的小鼠急性肺损伤。
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鲁格兰多苷通过抗炎和抗凋亡作用减轻小鼠脂多糖诱导的急性呼吸窘迫综合征。

Lugrandoside attenuates LPS-induced acute respiratory distress syndrome by anti-inflammation and anti-apoptosis in mice.

作者信息

Li Chengbao, Huang Ying, Yao Xueya, Hu Baoji, Wu Suzhen, Chen Guannan, Lv Xin, Tian Fubo

机构信息

Department of Anesthesiology, Shanghai Pulmonary Hospital, Tongji University School of MedicineShanghai, China; Department of Medicine, Hebei North UniversityZhangjiakou, Hebei, China.

Jiangsu Province Key Laboratory of Anesthesiology and Jiangsu Province Key Laboratory of Anesthesia and Analgesia Application Technology, Xuzhou Medical University Xuzhou, China.

出版信息

Am J Transl Res. 2016 Dec 15;8(12):5557-5568. eCollection 2016.

PMID:28078026
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5209506/
Abstract

This study aimed to investigate the protective effects and specific mechanisms of lugrandoside (LG) on lipopolysaccharides (LPS)-induced acute respiratory distress syndrome (ARDS). LG is a novel phenylpropanoid glycoside with many biological properties, isolated from the culinary leaves of Digitalis lutea L. and Digitalis grandiflora Miller. The primary indicators to assess the lung injury were infiltration of inflammatory cells; pulmonary edema; expression of proinflammatory cytokines, cyclo-oxygenase 2, and intracellular adhesion molecule 1; activation of nuclear factor-κB pathways; and cellular apoptosis. The results showed that LG evidently alleviated the inflammatory response, decreased the apoptosis of alveolar macrophages, and improved the lung injury in mice with LPS-induced ARDS. In conclusion, LG improved LPS-induced ARDS by anti-inflammation and anti-apoptosis and might be a promising pharmacological therapy for ARDS.

摘要

本研究旨在探讨鲁格兰糖苷(LG)对脂多糖(LPS)诱导的急性呼吸窘迫综合征(ARDS)的保护作用及具体机制。LG是一种具有多种生物学特性的新型苯丙素糖苷,从黄花毛地黄和大花毛地黄的烹饪叶中分离得到。评估肺损伤的主要指标包括炎性细胞浸润、肺水肿、促炎细胞因子、环氧化酶2和细胞间黏附分子1的表达、核因子-κB通路的激活以及细胞凋亡。结果表明,LG明显减轻了炎症反应,减少了肺泡巨噬细胞的凋亡,并改善了LPS诱导的ARDS小鼠的肺损伤。总之,LG通过抗炎和抗凋亡改善了LPS诱导的ARDS,可能是一种有前景的ARDS药物治疗方法。