Literature DB >> 25012041

Protective mechanism of Panax notoginseng saponins on rat hemorrhagic shock model in recovery stage.

Huai-Zheng Liu1, Zuo-Liang Liu, Shang-Ping Zhao, Chuan-Zheng Sun, Ming-Shi Yang.   

Abstract

To explore protective mechanism of Panax notoginseng saponins (PNS) on rat hemorrhagic shock model in recovery stage. 72 Wistar rats were selected and divided into control group, model group and PNS group with 24 rats in each group. 200 mg/kg PNS was injected intravenously at 60 min of hemorrhagic shock stage in PNS groups. Changes of endotoxin, MPO, IL-6, SOD, MDA and TNF α were observed at 30 and 120 min of recovery stage by ELISA; water content of lung and intestine was detected; HE staining was applied to observe morphological change of intestinal mucosa, kidney, liver and lung; western blot was used to detect intercellular adhesion molecule-1 (ICAM-1) level in lung tissue and intestine tissue. At 30 min and 120 min of recovery stage, MDA, MPO, endotoxin, TNF α and IL-6 levels significantly increased in model group compared with control group, however SOD level significantly decreased, the difference was statistically significant (P < 0.05); PNS dose-dependently decreased MDA, MPO, endotoxin, TNF α and IL-6 levels, and increased SOD level, which was statistically significant (P < 0.05); In results of water content detection, water content in lung tissue and intestine tissue was significantly higher than in control group, however, after being treated with PNS, the water content was significantly decreased; HE staining showed the morphologic change of lung tissue cells; Western blot showed that in lung tissue and intestine tissue, ICAM-1 level in model group was significantly higher than in control group, and it was lower in PNS group than in model group. PNS can increase SOD activity, decrease levels of MDA, endotoxin and MPO, decrease expression of TNF α and IL-6, and decrease water content in lung tissue and intestine tissue. Thus, PNS is protective to rat hemorrhagic shock model by anti oxidative stress and anti-inflammatory pathways, and ICAM-1 may play an important role in the mechanism.

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Year:  2014        PMID: 25012041     DOI: 10.1007/s12013-014-0119-x

Source DB:  PubMed          Journal:  Cell Biochem Biophys        ISSN: 1085-9195            Impact factor:   2.194


  4 in total

1.  Panax notoginseng saponins promote wound repair of anterior cruciate ligament through phosphorylation of PI3K, AKT and ERK.

Authors:  Lu Yu; Jingwei Xie; Na Xin; Zhanyou Wang
Journal:  Int J Clin Exp Pathol       Date:  2015-01-01

2.  Intervention Effects of Atorvastatin Combined with Panax notoginseng Saponins on Rats with Atherosclerosis Complicated with Hepatic Injury.

Authors:  Qing-Fang Jiang; Min-Yi Huang; Kang-Yuan Wu; Jie-Ling Weng; Rong-Gui Deng; Xin-Jie Xu; Jian-Pei Xu; Tao Jiang
Journal:  Pharmacogn Mag       Date:  2017-07-19       Impact factor: 1.085

Review 3.  Panax notoginseng Saponins for Treating Coronary Artery Disease: A Functional and Mechanistic Overview.

Authors:  Lian Duan; Xingjiang Xiong; Junyuan Hu; Yongmei Liu; Jun Li; Jie Wang
Journal:  Front Pharmacol       Date:  2017-10-17       Impact factor: 5.810

4.  Chronic saponin treatment attenuates damage to the pancreas in chronic alcohol-treated diabetic rats.

Authors:  Mi Ran Choi; Su Min Kwak; Sol Hee Bang; Jo-Eun Jeong; Dai-Jin Kim
Journal:  J Ginseng Res       Date:  2016-10-05       Impact factor: 6.060

  4 in total

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