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血必净注射液与消退素D1协同调节脓毒症诱导的肺损伤小鼠的白细胞黏附并提高存活率。

Xuebijing Injection () and Resolvin D1 Synergize Regulate Leukocyte Adhesion and Improve Survival Rate in Mice with Sepsis-Induced Lung Injury.

作者信息

Zhang Shu-Kun, Zhuo Yu-Zhen, Li Cai-Xia, Yang Lei, Gao Hong-Wei, Wang Xi-Mo

机构信息

Department of Cell and Molecular Biology, Institute of Acute Abdominal Diseases of Intergrated Traditional Chinese and Western Medicine, Tianjin Nankai Hospital, Tianjin, 300100, China.

Center for Experimental Therapeutics and Reperfusion Injury, Department of Anesthesiology, Perioperative and Pain Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 02115, USA.

出版信息

Chin J Integr Med. 2018 Apr;24(4):272-277. doi: 10.1007/s11655-017-2959-x. Epub 2017 May 17.

Abstract

OBJECTIVE

To investigate the effect of combined application of Xuebijing Injection ( , XBJ) and resolvin D1 (RvD1) on survival rate and the underlying mechanisms in mice with sepsisinduced lung injury.

METHODS

The cecal ligation and puncture (CLP) method was used to develop a mouse sepsis model. Specific pathogen free male C57BL/6 mice were randomly divided into 5 groups (n=20 each): sham, CLP, CLP+XBJ, CLP+RvD1 and CLP+XBJ+RvD1. After surgery, mice in the CLP+XBJ, CLP+RvD1 and CLP+XBJ+RvD1 groups were given XBJ (25 μL/g body weight), RvD1 (10 ng/g body weight), and their combination (the same dose of XBJ and RvD1), respectively. In each group, 12 mice were used to observe 1-week survival rate, while the rest were executed at 12 h. Whole blood was collected for flow cytometric analysis of leukocyte adhesion molecules CD18, lung tissues were harvested for observing pathological changes, and testing the activity of myeloperoxidase (MPO) and the expression of intercellular cell adhesion molecule 1 (ICAM-1).

RESULTS

Compared with the CLP group, the histopathological damage of the lung tissues was mitigated, MPO activity was decreased in the CLP+XBJ and CLP+RvD1 groups (P<0.05). In addition, the 1-week survival rate was improved, proportion of CD18-expressing cells in whole blood and ICAM-1 protein expression in lung tissue were decreased in the CLP+XBJ+RvD1 group (P<0.05 or P<0.01).

CONCLUSIONS

XBJ together with RvD1 could effectively inhibit leukocyte adhesion, reduce lung injury, and improve the survival rate of mice with sepsis.

摘要

目的

探讨血必净注射液(XBJ)与消退素D1(RvD1)联合应用对脓毒症诱导的肺损伤小鼠存活率的影响及其潜在机制。

方法

采用盲肠结扎穿孔(CLP)法建立小鼠脓毒症模型。将无特定病原体的雄性C57BL/6小鼠随机分为5组(每组n = 20):假手术组、CLP组、CLP + XBJ组、CLP + RvD1组和CLP + XBJ + RvD1组。术后,CLP + XBJ组、CLP + RvD1组和CLP + XBJ + RvD1组小鼠分别给予XBJ(25 μL/g体重)、RvD1(10 ng/g体重)及其组合(相同剂量的XBJ和RvD1)。每组中,12只小鼠用于观察1周存活率,其余小鼠在12 h处死。采集全血用于白细胞黏附分子CD18的流式细胞术分析,获取肺组织用于观察病理变化,并检测髓过氧化物酶(MPO)活性和细胞间黏附分子1(ICAM - 1)的表达。

结果

与CLP组相比,CLP + XBJ组和CLP + RvD1组肺组织的组织病理学损伤减轻,MPO活性降低(P < 0.05)。此外,CLP + XBJ + RvD1组1周存活率提高,全血中表达CD18的细胞比例和肺组织中ICAM - 1蛋白表达降低(P < 0.05或P < 0.01)。

结论

XBJ与RvD1联合应用可有效抑制白细胞黏附,减轻肺损伤,提高脓毒症小鼠的存活率。

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