Protective Mechanism of Panax notoginseng Saponins on Rat Hemorrhagic Shock Model in Recovery Stage

Cell Biochemistry and Biophysics

Volumn 70, Issue 3, 2014, Pages 1719-1724

  Liu, Huai Zheng ^a   Liu, Zuo Liang ^a   Zhao, Shang Ping ^a   Sun, Chuan Zheng ^a   Yang, Ming Shi ^a  

^a THE THIRD XIANGYA HOSPITAL OF CENTRAL SOUTH UNIVERSITY   (China)

Author keywords

Hemorrhagic shock; ICAM 1; Panax notoginseng saponins; Recovery stage

Indexed keywords

ENDOTOXIN; INTERCELLULAR ADHESION MOLECULE 1; INTERLEUKIN 6; MALONALDEHYDE; PEROXIDASE; PROTECTIVE AGENT; SAPONIN; SUPEROXIDE DISMUTASE; TUMOR NECROSIS FACTOR ALPHA;

ANIMAL; BLOOD; CHEMISTRY; DISEASE MODEL; ENZYME LINKED IMMUNOSORBENT ASSAY; LUNG; MALE; METABOLISM; PANAX NOTOGINSENG; PATHOLOGY; RAT; SHOCK, HEMORRHAGIC; WISTAR RAT;

ANIMALS; DISEASE MODELS, ANIMAL; ENDOTOXINS; ENZYME-LINKED IMMUNOSORBENT ASSAY; INTERCELLULAR ADHESION MOLECULE-1; INTERLEUKIN-6; LUNG; MALE; MALONDIALDEHYDE; PANAX NOTOGINSENG; PEROXIDASE; PROTECTIVE AGENTS; RATS; RATS, WISTAR; SAPONINS; SHOCK, HEMORRHAGIC; SUPEROXIDE DISMUTASE; TUMOR NECROSIS FACTOR-ALPHA;

EID: 84939872393     PISSN: 10859195     EISSN: 15590283     Source Type: Journal    
DOI: 10.1007/s12013-014-0119-x     Document Type: Article

References (30)

1. Spinella, P. C., & Holcomb, J. B. (2009). Resuscitation and transfusion principles for traumatic hemorrhagic shock. Blood Reviews,23(6), 231–240.
2. Fan, J., Li, Y., Levy, R. M., Fan, J. J., Hackam, D. J., Vodovotz, Y., et al. (2007). Hemorrhagic shock induces NAD(P)H oxidase activation in neutrophils: Role of HMGB1-TLR4 signaling. Journal of Immunology,178(10), 6573–6580.
3. Zuckerbraun, B. S., McCloskey, C. A., Gallo, D., Liu, F., Ifedigbo, E., Otterbein, L. E., et al. (2005). Carbon monoxide prevents multiple organ injury in a model of hemorrhagic shock and resuscitation. Shock,23(6), 527–532.
4. Perl, M., Chung, C. S., Lomas-Neira, J., Rachel, T. M., Biffl, W. L., Cioffi, W. G., et al. (2005). Silencing of Fas, but not caspase-8, in lung epithelial cells ameliorates pulmonary apoptosis, inflammation, and neutrophil influx after hemorrhagic shock and sepsis. The American Journal of Pathology,167(6), 1545–1559.
5. Xu, J., & Liu, L. (2005). The role of calcium desensitization in vascular hyporeactivity and its regulation after hemorrhagic shock in the rat. Shock,23(6), 576–581.
6. Moore, E. E., Moore, F. A., Fabian, T. C., Bernard, A. C., Fulda, G. J., Hoyt, D. B., et al. (2009). Human polymerized hemoglobin for the treatment of hemorrhagic shock when blood is unavailable: The USA multicenter trial. Journal of the American College of Surgeons,208(1), 1–13.
7. Thuijls, G., de Haan, J. J., Derikx, J. P., Daissormont, I., Hadfoune, M., Heineman, E., et al. (2009). Intestinal cytoskeleton degradation precedes tight junction loss following hemorrhagic shock. Shock,31(2), 164–169.
8. Liu, H., Yang, J., Du, F., Gao, X., Ma, X., Huang, Y., et al. (2009). Absorption and disposition of ginsenosides after oral administration of Panax notoginseng extract to rats. Drug Metabolism and Disposition: The Biological Fate of Chemicals,37(12), 2290–2298.
9. Wang, C. Z., Xie, J. T., Fishbein, A., Aung, H. H., He, H., Mehendale, S. R., et al. (2009). Antiproliferative effects of different plant parts of Panax notoginseng on SW480 human colorectal cancer cells. Phytotherapy Research: PTR,23(1), 6–13.
10. Li, J., Xie, Z. Z., Tang, Y. B., Zhou, J. G., & Guan, Y. Y. (2011). Ginsenoside-Rd, a purified component from Panax notoginseng saponins, prevents atherosclerosis in apoE knockout mice. European Journal of Pharmacology,652(1–3), 104–110.
11. Si, Y. C., Zhang, J. P., Xie, C. E., Zhang, L. J., & Jiang, X. N. (2011). Effects of Panax notoginseng saponins on proliferation and differentiation of rat hippocampal neural stem cells. The American Journal of Chinese Medicine,39(5), 999–1013.
12. Hu, Z., Yang, J., Cheng, C., Huang, Y., Du, F., Wang, F., et al. (2013). Combinatorial metabolism notably affects human systemic exposure to ginsenosides from orally administered extract of Panax notoginseng roots (Sanqi). Drug Metabolism and Disposition: The Biological Fate of Chemicals,41(7), 1457–1469.
13. Chen, S., Liu, J., Liu, X., Fu, Y., Zhang, M., Lin, Q., et al. (2011). Panax notoginseng saponins inhibit ischemia-induced apoptosis by activating PI3K/Akt pathway in cardiomyocytes. Journal of Ethnopharmacology,137(1), 263–270.
14. Fan, J. S., Liu, D. N., Huang, G., Xu, Z. Z., Jia, Y., Zhang, H. G., et al. (2012). Panax notoginseng saponins attenuate atherosclerosis via reciprocal regulation of lipid metabolism and inflammation by inducing liver X receptor alpha expression. Journal of Ethnopharmacology,142(3), 732–738.
15. Li, T., Zhu, Y., Hu, Y., Li, L., Diao, Y., Tang, J., et al. (2011). Ideal permissive hypotension to resuscitate uncontrolled hemorrhagic shock and the tolerance time in rats. Anesthesiology,114(1), 111–119.
16. Li, Y., Xiang, M., Yuan, Y., Xiao, G., Zhang, J., Jiang, Y., et al. (2009). Hemorrhagic shock augments lung endothelial cell activation: role of temporal alterations of TLR4 and TLR2. American Journal of Physiology: Regulatory, Integrative and Comparative Physiology,297(6), R1670–R1680.
17. Legrand, M., Mik, E. G., Balestra, G. M., Lutter, R., Pirracchio, R., Payen, D., et al. (2010). Fluid resuscitation does not improve renal oxygenation during hemorrhagic shock in rats. Anesthesiology,112(1), 119–127.
18. Park, K. H., Lee, K. H., Kim, H., & Hwang, S. O. (2010). The anti-inflammatory effects of ulinastatin in trauma patients with hemorrhagic shock. Journal of Korean Medical Science,25(1), 128–134.
19. Takahashi, T., Shimizu, H., Morimatsu, H., Maeshima, K., Inoue, K., Akagi, R., et al. (2009). Heme oxygenase-1 is an essential cytoprotective component in oxidative tissue injury induced by hemorrhagic shock. Journal of Clinical Biochemistry and Nutrition,44(1), 28–40.
20. Li, X. D., Chang, B., Chen, B., Liu, Z. Y., Liu, D. X., Wang, J. S., et al. (2010). Panax notoginseng saponins potentiate osteogenesis of bone marrow stromal cells by modulating gap junction intercellular communication activities. Cellular Physiology and Biochemistry: International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology,26(6), 1081–1092.
21. Yu, M. L., Zhang, C. L., Yuan, D. D., Tong, X. H., & Tao, L. (2012). Panax notoginseng saponins enhances the cytotoxicity of cisplatin via increasing gap junction intercellular communication. Biological and Pharmaceutical Bulletin,35(8), 1230–1237.
22. Huang, J., Wu, D., Wang, J., Li, F., Lu, L., Gao, Y., et al. (2014). Effects of Panax notoginseng saponin on alpha, beta, and gamma secretase involved in Abeta deposition in SAMP8 mice. NeuroReport,25(2), 89–93.
23. Liu, Y., Zhang, H. G., Jia, Y., & Li, X. H. (2010). Panax notoginseng saponins attenuate atherogenesis accelerated by zymosan in rabbits. Biological and Pharmaceutical Bulletin,33(8), 1324–1330.
24. Ma, L., Cao, Y. H., Cheng, M. H., Huang, Y., Mo, M. H., Wang, Y., et al. (2013). Phylogenetic diversity of bacterial endophytes of Panax notoginseng with antagonistic characteristics towards pathogens of root-rot disease complex. Antonie van Leeuwenhoek,103(2), 299–312.
25. Van Raamsdonk, J. M., & Hekimi, S. (2012). Superoxide dismutase is dispensable for normal animal lifespan. Proceedings of the National Academy of Sciences of USA,109(15), 5785–5790.
26. Munch, C., O’Brien, J., & Bertolotti, A. (2011). Prion-like propagation of mutant superoxide dismutase-1 misfolding in neuronal cells. Proceedings of the National Academy of Sciences of the USA,108(9), 3548–3553.
27. Park, E. J., Lee, J. H., Yu, G. Y., He, G., Ali, S. R., Holzer, R. G., et al. (2010). Dietary and genetic obesity promote liver inflammation and tumorigenesis by enhancing IL-6 and TNF expression. Cell,140(2), 197–208.
28. Gang, H., Shaw, J., Dhingra, R., Davie, J. R., & Kirshenbaum, L. A. (2013). Epigenetic regulation of canonical TNFalpha pathway by HDAC1 determines survival of cardiac myocytes. American Journal of Physiology Heart and Circulatory Physiology,304(12), H1662–H1669.
29. Csak, T., Ganz, M., Pespisa, J., Kodys, K., Dolganiuc, A., & Szabo, G. (2011). Fatty acid and endotoxin activate inflammasomes in mouse hepatocytes that release danger signals to stimulate immune cells. Hepatology,54(1), 133–144.
30. Nicholls, S. J., Tang, W. H., Brennan, D., Brennan, M. L., Mann, S., Nissen, S. E., et al. (2011). Risk prediction with serial myeloperoxidase monitoring in patients with acute chest pain. Clinical Chemistry,57(12), 1762–1770.