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Anti-Inflammation Effects and Potential Mechanism of Saikosaponins by Regulating Nicotinate and Nicotinamide Metabolism and Arachidonic Acid Metabolism

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Abstract

Inflammation is an important immune response; however, excessive inflammation causes severe tissue damages and secondary inflammatory injuries. The long-term and ongoing uses of routinely used drugs such as non-steroidal anti-inflammatory drugs (NSAIDS) are associated with serious adverse reactions, and not all patients have a well response to them. Consequently, therapeutic products with more safer and less adverse reaction are constantly being sought. Radix Bupleuri, a well-known traditional Chinese medicine (TCM), has been reported to have anti-inflammatory effects. However, saikosaponins (SS) as the main pharmacodynamic active ingredient, their pharmacological effects and action mechanism in anti-inflammation have not been reported frequently. This study aimed to explore the anti-inflammatory activity of SS and clarify the potential mechanism in acute inflammatory mice induced by subcutaneous injection of formalin in hind paws. Paw edema was detected as an index to evaluate the anti-inflammatory efficacy of SS. Then, a metabolomic method was used to investigate the changed metabolites and potential mechanism of SS. Metabolite profiling was performed by high-performance liquid chromatography combined with quadrupole time-of-flight mass spectrometry (HPLC-Q-TOF-MS). The detection and identification of the changed metabolites were systematically analyzed by multivariate data and pathway analysis. As a result, 12 different potential biomarkers associated with SS in anti-inflammation were identified, including nicotinate, niacinamide, arachidonic acid (AA), and 20-carboxy-leukotriene B4, which are associated with nicotinate and nicotinamide metabolism and arachidonic acid metabolism. The expression levels of biomarkers were effectively modulated towards the normal range by SS. It indicated that SS show their effective anti-inflammatory effects through regulating nicotinate and nicotinamide metabolism and arachidonic acid metabolism.

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References

  1. Johnston, J., S. Basatvat, Z. Ilyas, et al. 2015. Tribbles in inflammation. Biochemical Society Transactions 43: 1069–1070.

    Article  CAS  PubMed  Google Scholar 

  2. Lee, I.T., and C.M. Yang. 2012. Role of NADPH oxidase/ROS in pro-inflammatory mediators-induced airway and pulmonary diseases. Biochemical Pharmacology 84: 581–590.

    Article  CAS  PubMed  Google Scholar 

  3. Saxena, A., D. Yadav, A.K. Maurya, et al. 2016. Diarylheptanoids from Alnus nepalensis attenuates LPS-induced inflammation in macrophages and endotoxic shock in mice. International Immunopharmacology 30: 129–136.

    Article  CAS  PubMed  Google Scholar 

  4. Xubo, S., and D. Hu. 2008. The mechanism of aspirin and related clinical problems of clinical focus. Clinical Metabolism 23: 1141–1143.

    Google Scholar 

  5. Kim, S.H., M. Sanak, and H.S. Park. 2013. Genetics of hypersensitivityto aspirin and nonsteroidal anti-inflammatory drugs. Immunology and Allergy Clinics of North America 33: 177–194.

    Article  PubMed  Google Scholar 

  6. Chunxiao, L., Z. Yang, and L. Chengjian. 2011. The rare adverse drug reaction of aspirin. Journal of Medical Science in China 11: 1686.

    Google Scholar 

  7. Park, Y., S.M. Jung, S.A. Yoo, et al. 2015. Antinociceptive and anti-inflammatory effects of essential oil extracted from Chamaecyparis obtusa in mice. International Immunopharmacology 29: 320–325.

    Article  CAS  PubMed  Google Scholar 

  8. National Commission of Chinese Pharmacopoeia. 2015. Pharmacopoeia of People’s Republic of China, vol. 1, 263–264. Beijing: Chemical Industry Press.

    Google Scholar 

  9. Ashour, M.L., and M. Wink. 2011. Genus Bupleurum: a review of its phytochemistry. Pharmacology and modes of action. Journal of Pharmacy and Pharmacology 63: 305–321.

    Article  CAS  PubMed  Google Scholar 

  10. Zhu, J., C. Luo, P. Wang, et al. 2013. Saikosaponin A mediates the inflammatory response by inhibiting the MAPK and NF-κB pathways in LPS-stimulated RAW 264.7 cells. Experimental and Therapeutic Medicine 5: 1345–1350.

    CAS  PubMed  PubMed Central  Google Scholar 

  11. Wu, G.C., H. Wu, L.Y. Fan, et al. 2011. Saikosaponins: a potential treatment option for systemic lupus erythematosus. Irish Journal of Medical Science 180: 259–261.

    Article  PubMed  Google Scholar 

  12. Sui, C., J. Zhang, J. Wei, et al. 2011. Transcriptome analysis of Bupleurum chinense focusing on genes involved in the biosynthesis of saikosaponins. BMC Genomics 12: 539.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  13. Lee.TH, Park.SH, You.MH, et al (2015) A potential therapeutic effect of saikosaponin C as a novel dual-target anti-Alzheimer agent. J Neurochem

  14. Wong, V.K., H. Zhou, and S.S. Cheung. 2009. Mechanistic study of saikosaponin-d (Ssd) on suppression of murine T lymphocyte activation. Journal of Cellular Biochemistry 107: 303.

    Article  CAS  PubMed  Google Scholar 

  15. Zhao, L.C., H. Zhang, J.F. Bao, et al. 2015. Saikosaponin-d protects renal tubular epithelial cell against high glucose induced injury through modulation of SIRT3. International Journal of Clinical Experimental Medicine 8: 6472–6473.

    CAS  PubMed  PubMed Central  Google Scholar 

  16. Chun, J., A. Tosun, and Y.S. Kim. 2016. Anti-inflammatory effect of corymbocoumarin from Seseli gummiferum subsp. corymbosum through suppression of NF-κB signaling pathway and induction of HO-1 expression in LPS-stimulated RAW 264.7 cells. International Immunopharmacology 31: 207–215.

    Article  CAS  PubMed  Google Scholar 

  17. Kleiner, M., C. Wentrup, C. Lott, et al. 2012. Metaproteomics of a gutless marine worm and its symbiotic microbial community reveal unusual pathways for carbon and energy use. Proceedings of the National Academy of Sciences of the United States of America 109: 1173–82.

    Article  Google Scholar 

  18. Zhang, A., H. Sun, X. Wu, et al. 2012. Urine metabolomics. Clinica Chimica Acta 414: 65–69.

    Article  CAS  Google Scholar 

  19. ZhangA, S.H., and X. Wang. 2012. Recent highlights of metabolomics for traditional Chinese medicine. Pharmazie 67: 667–675.

    Google Scholar 

  20. Sun, H., A. Zhang, and X. Wang. 2012. Potential role of metabolomic approaches for Chinese medicine syndromes and herbal medicine. Phytotherapy Research 26: 1466–1471.

    Article  CAS  PubMed  Google Scholar 

  21. Hong gang, N. 2010. Lipid profiling of rat peritoneal surface layers by online normal and reversed-phase 2D LC-Q-TOF-MS. Journal of Lipid Research 51: 2833–2844.

    Article  Google Scholar 

  22. Liu, J.L., and H.L. Wang. 2011. Metabonomics study of brain-specific human S100B transgenic mice by using high-performance liquid chromatography coupled with quadrupole time of flight mass spectrometry. Biological and Pharmaceutical Bulletin 34: 871–876.

    Article  CAS  PubMed  Google Scholar 

  23. Lin, G., and C. Liu. 2012. Metabolomic analysis reveals differences in umbilical vein plasma metabolites between normal and growth-restricted fetal pigs during late gestation. Journal of Nutrition 14: 990–998.

    Article  Google Scholar 

  24. Gao, W., and H. Yang. 2012. Unbiased metabolite profiling by liquid chromatography–quadrupole time-of-flight mass spectrometry and multivariate data analysis for herbal authentication: Classification of seven Lonicera species flower buds. Journal of Chromatography A 1245: 109–116.

    Article  CAS  PubMed  Google Scholar 

  25. Hargreaves, K., R. Dubner, F. Brown, et al. 1988. A new and sensitive method for measuring thermal nocicep-tion in cutaneous hyperalgesia. Pain 32: 77–88.

    Article  CAS  PubMed  Google Scholar 

  26. Iadarola, M.J., L.S. Brady, G. Draisci, et al. 1988. Enhancement of dynorphin gene expression in spinal cord following experimental inflammation: stimulus specificity, be-havioral parameters and opioid receptor binding. Pain 35: 313–326.

    Article  CAS  PubMed  Google Scholar 

  27. Millan, M.J., A. Czlonkowski, B. Morris, et al. 1988. Inflammation of the hind limb as a model of unilateral, localized pain: influence on multiple opioid systems in the spinal cord of the rat. Pain 35: 299–312.

    Article  CAS  PubMed  Google Scholar 

  28. Medzhitov, R. 2010. Inflammation, new adventures of an old flame. Cell 140: 771–776.

    Article  CAS  PubMed  Google Scholar 

  29. MHuston, J., and K.J. Tracey. 2011. The pulse of inflammation: heart rate variability, the cholinergic anti-inflammatory pathway and implications for therapy. Journal of Internal Medicine 269: 45–53.

    Article  Google Scholar 

  30. Yang, Y.Y., Y.Z. Tang, C.L. Fan, et al. 2010. Identification and determination of the saikosaponins in Radix bupleuri by accelerated solvent extraction combined with rapid-resolution LC-MS. Journal of Separation Science 33: 1933–1945.

    Article  CAS  PubMed  Google Scholar 

  31. Penberthy, W.T. 2009. Nicotinamide adenine dinucleotide biology and disease. Current Pharmaceutical Design 15: 1–2.

    Article  PubMed  Google Scholar 

  32. Zhai, R.G., M. Rizzi, and S. Garavaglia. 2009. Nicotinamide/nicotinic acid mononucleotide adenylyltransferase, new insights into an ancient enzyme. Cellular and Molecular Life Sciences 66: 2805–2818.

    Article  CAS  PubMed  Google Scholar 

  33. Sampath, D., T.S. Zabka, D.L. Misner, et al. 2015. Inhibition of nicotinamide phosphoribosyltransferase (NAMPT) as a therapeutic strategy in cancer. Pharmacology and Therapeutics 151: 16–31.

    Article  CAS  PubMed  Google Scholar 

  34. Luk, T., Z. Malam, and J.C. Marshall. 2008. Pre-b cell colony-enhancing factor (PBEF)/visfatin: a novel mediator of innate immunity. Journal of Leukocyte Biology 83: 804–816.

    Article  CAS  PubMed  Google Scholar 

  35. Sasaki, H., T. Matsushita, and K. Takayama. 2013. The overexpression of SIRT1 inhibited osteoarthritic gene expression changes induced by interleukin-1β in human chondrocytes. Journal of Orthopaedic Research 31: 531–537.

    Article  PubMed  Google Scholar 

  36. Imai, S. 2009. The NAD world: a new systemic regulatory network for metabolism and aging-Sirt1, systemic NAD biosynthesis, and their importance. Cell Biochemistry and Biophysics 53: 265–274.

    Article  Google Scholar 

  37. Revollo, J.R., A.A. Grimm, and S. Imai. 2007. The regulation of nicotinamide adenine dinucleotide biosynthesis by Nampt/PBEF/visfatin in mammals. Current Opinion in Gastroenterology 23: 164–170.

    Article  CAS  PubMed  Google Scholar 

  38. Dai, J., X. Zhang, and L. Lin. 2014. Energy sensitive AMPK-SIRT1 pathway and inflammation regulation. Life Sciences 26: 362–365.

    Google Scholar 

  39. Palmetshofer, A., S.C. Robson, and V. Nehls. 1999. Lysophosphatidic acid activates nuclear factor kappa B and induces proinflammatory gene expression in endothelial cells. Thrombosis and Haemostasis 82: 1532–1537.

    CAS  PubMed  Google Scholar 

  40. Harder, D.R., W.B. Campbe, R.J. Roman, et al. 1995. Role of cytochrome P450 enzymes and metabolites of arachidonic acid in the control of vascular tone. Journal of Vascular Research 32: 79–92.

    Article  CAS  PubMed  Google Scholar 

  41. Shoeb, M., U.C. Yadav, S.K. Srivastava, et al. 2011. Inhibition of aldose reductase prevents endotoxin-induced inflammation by regulating arachidonic acid pathway in murine macrophages. Free Radical Biology and Medicine 51: 1686–1696.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  42. Jeon, S.G., H.G. Moon, Y.S. Kim, et al. 2009. 15-lipoxygenase metabolites play an important role in the development of a T-helper type 1 allergic inflammation induced by double-stranded RNA. Clinical and Experimental Allergy 39: 908–917.

    Article  CAS  PubMed  Google Scholar 

  43. Martel-Pelletier, J., D. Lajeunesse, and P. Reboul. 2003. Therapeutic role of dual inhibitors of 5-LOX and COX, selective and non-selective non-steroidal anti-inflammatory drugs. Annals of the Rheumatic Diseases 62: 501–509.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

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Acknowledgments

This study was supported by grants from the National Natural Science Foundation of China (No. 81241111) and the project of institutions of higher learning talents to support in Liaoning province (No. LR2013044).

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Correspondence to Xiansheng Meng.

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All experiments were carried out in accordance with the approved experimental animal protocols and guidelines established by Medicine Ethics Review Committee of Liaoning University of Traditional Chinese Medicine.

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Yu Ma and Yongrui Bao contributed equally to this work.

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Ma, Y., Bao, Y., Wang, S. et al. Anti-Inflammation Effects and Potential Mechanism of Saikosaponins by Regulating Nicotinate and Nicotinamide Metabolism and Arachidonic Acid Metabolism. Inflammation 39, 1453–1461 (2016). https://doi.org/10.1007/s10753-016-0377-4

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