References
- East, J. 1955. The effect of certain plant preparations on the fertility of laboratory mammals. 4. Sanguisorba officinalis L. J. Endocrinol. 12: 273-276. https://doi.org/10.1677/joe.0.0120273
- Park, K. H., D. Koh, K. Kim, J. Park, and Y. Lim. 2004. Antiallergic activity of a disaccharide isolated from Sanguisorba officinalis. Phytother. Res. 18: 658-662. https://doi.org/10.1002/ptr.1545
- Goun, E. A., V. M. Petrichenko, S. U. Solodnikov, T. V. Suhinina, M. A. Kline, G. Cunningham, C. Nguyen, and H. Miles. 2002. Anticancer and antithrombin activity of Russian plants. J. Ethnopharmacol. 81: 337-342. https://doi.org/10.1016/S0378-8741(02)00116-2
- Kim, Y. H., C. B. Chung, J. G. Kim, K. I. Ko, S. H. Park, J. H. Kim, S. Y. Eom, Y. S. Kim, Y. I. Hwang, and K. H. Kim. 2008. Anti-wrinkle activity of ziyuglycoside I isolated from a Sanguisorba officinalis root extract and its application as a cosmeceutical ingredient. Biosci. Biotechnol. Biochem. 72: 303-311. https://doi.org/10.1271/bbb.70268
- Ban, J. Y., H. T. Nguyen, H. J. Lee, S. O. Cho, H. S. Ju, J. Y. Kim, K. Bae, K. S. Song, and Y. H. Seong. 2008. Neuroprotective properties of gallic acid from Sanguisorbae radix on amyloid beta protein (25--35)-induced toxicity in cultured rat cortical neurons. Biol. Pharm. Bull. 31: 149-153. https://doi.org/10.1248/bpb.31.149
- Wang, Z., W. T. Loo, N. Wang, L. W. Chow, D. Wang, F. Han, X. Zheng, and J. P. Chen. 2012. Effect of Sanguisorba officinalis L on breast cancer growth and angiogenesis. Expert Opin. Ther. Targets 16 Suppl 1: S79-89. https://doi.org/10.1517/14728222.2011.642371
- Tsukahara, K., S. Moriwaki, T. Fujimura, and Y. Takema. 2001. Inhibitory effect of an extract of Sanguisorba officinalis L. on ultraviolet-B-induced photodamage of rat skin. Biol. Pharm. Bull. 24: 998-1003. https://doi.org/10.1248/bpb.24.998
- Liu, X., Y. Cui, Q. Yu, and B. Yu. 2005. Triterpenoids from Sanguisorba officinalis. Phytochemistry 66: 1671-1679. https://doi.org/10.1016/j.phytochem.2005.05.011
- Mimaki, Y., M. Fukushima, A. Yokosuka, Y. Sashida, S. Furuya, and H. Sakagami. 2001. Triterpene glycosides from the roots of Sanguisorba officinalis. Phytochemistry 57: 773-779. https://doi.org/10.1016/S0031-9422(01)00083-8
- Cho, J. Y., E. S. Yoo, B. C. Cha, H. J. Park, M. H. Rhee, and Y. N. Han. 2006. The inhibitory effect of triterpenoid glycosides originating from Sanguisorba officinalis on tissue factor activity and the production of TNF-alpha. Planta Med. 72: 1279-1284. https://doi.org/10.1055/s-2006-947257
- Choi, J., M. Y. Kim, B. C. Cha, E. S. Yoo, K. Yoon, J. Lee, H. S. Rho, S. Y. Kim, and J. Y. Cho. 2012. ZYM-201 sodium succinate ameliorates streptozotocin-induced hyperlipidemic conditions. Planta Med. 78: 12-17. https://doi.org/10.1055/s-0031-1280219
- Choi, J., T. Yu, B. C. Cha, M. H. Rhee, E. S. Yoo, M. Y. Kim, J. Lee, and J. Y. Cho. 2011. Modulatory effects of ZYM-201 sodium succinate on dietary-induced hyperlipidemic conditions. Pharmazie 66: 791-797.
- Lu, Y. C., W. C. Yeh, and P. S. Ohashi. 2008. LPS/TLR4 signal transduction pathway. Cytokine 42: 145-151. https://doi.org/10.1016/j.cyto.2008.01.006
- Alexander, C., and E. T. Rietschel. 2001. Bacterial lipopolysaccharides and innate immunity. J. Endotoxin Res. 7: 167-202.
- Akira, S., and S. Sato. 2003. Toll-like receptors and their signaling mechanisms. Scand. J. Infect. Dis. 35: 555-562. https://doi.org/10.1080/00365540310015683
- Buss, H., A. Dorrie, M. L. Schmitz, E. Hoffmann, K. Resch, and M. Kracht. 2004. Constitutive and interleukin-1-inducible phosphorylation of p65 NF-{kappa}B at serine 536 is mediated by multiple protein kinases including I{kappa}B kinase (IKK)-{alpha}, IKK{beta}, IKK{epsilon}, TRAF family member-associated (TANK)-binding kinase 1 (TBK1), and an unknown kinase and couples p65 to TATA-binding protein-associated factor II31-mediated interleukin-8 transcription. J. Biol. Chem. 279: 55633-55643. https://doi.org/10.1074/jbc.M409825200
- Suvas, S., V. Singh, S. Sahdev, H. Vohra, and J. N. Agrewala. 2002. Distinct role of CD80 and CD86 in the regulation of the activation of B cell and B cell lymphoma. J. Biol. Chem. 277: 7766-7775. https://doi.org/10.1074/jbc.M105902200
- Ogata, H., I. Su, K. Miyake, Y. Nagai, S. Akashi, I. Mecklenbrauker, K. Rajewsky, M. Kimoto, and A. Tarakhovsky. 2000. The toll-like receptor protein RP105 regulates lipopolysaccharide signaling in B cells. J. Exp. Med. 192: 23-29. https://doi.org/10.1084/jem.192.1.23
- Collins, A. V., D. W. Brodie, R. J. Gilbert, A. Iaboni, R. Manso-Sancho, B. Walse, D. I. Stuart, P. A. van der Merwe, and S. J. Davis. 2002. The interaction properties of costimulatory molecules revisited. Immunity 17: 201-210. https://doi.org/10.1016/S1074-7613(02)00362-X
- Giannoukakis, N., C. A. Bonham, S. Qian, Z. Chen, L. Peng, J. Harnaha, W. Li, A. W. Thomson, J. J. Fung, P. D. Robbins, and L. Lu. 2000. Prolongation of cardiac allograft survival using dendritic cells treated with NF-kB decoy oligodeoxyribonucleotides. Mol. Ther. 1: 430-437. https://doi.org/10.1006/mthe.2000.0060
- Zhang, G., and S. Ghosh. 2001. Toll-like receptor-mediated NF-kappaB activation: a phylogenetically conserved paradigm in innate immunity. J. Clin. Invest. 107: 13-19. https://doi.org/10.1172/JCI11837
- Viatour, P., M. P. Merville, V. Bours, and A. Chariot. 2005. Phosphorylation of NF-kappaB and IkappaB proteins: implications in cancer and inflammation. Trends Biochem. Sci. 30: 43-52. https://doi.org/10.1016/j.tibs.2004.11.009
- Pierce, J. W., M. A. Read, H. Ding, F. W. Luscinskas, and T. Collins. 1996. Salicylates inhibit I kappa B-alpha phosphorylation, endothelial-leukocyte adhesion molecule expression, and neutrophil transmigration. J. Immunol. 156: 3961-3969.
- Yin, M. J., Y. Yamamoto, and R. B. Gaynor. 1998. The anti-inflammatory agents aspirin and salicylate inhibit the activity of I(kappa)B kinase-beta. Nature 396: 77-80. https://doi.org/10.1038/23948
- Yamamoto, Y., and R. B. Gaynor. 2001. Therapeutic potential of inhibition of the NF-kappaB pathway in the treatment of inflammation and cancer. J. Clin. Invest. 107: 135-142. https://doi.org/10.1172/JCI11914
Cited by
- Anti-Diabetic and Hepato-Renal Protective Effects of Ziyuglycoside II Methyl Ester in Type 2 Diabetic Mice vol.7, pp.7, 2014, https://doi.org/10.3390/nu7075232
- Anti-Inflammatory and Antinociceptive Activities of Anthraquinone-2-Carboxylic Acid vol.2016, pp.None, 2014, https://doi.org/10.1155/2016/1903849
- Syk and IRAK1 Contribute to Immunopharmacological Activities of Anthraquinone-2-carboxlic Acid vol.21, pp.6, 2014, https://doi.org/10.3390/molecules21060809
- Phytotherapeutic Activities of Sanguisorba officinalis and its Chemical Constituents: A Review vol.46, pp.2, 2014, https://doi.org/10.1142/s0192415x18500155