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DOI QR Code

Serotonins of safflower seeds play a key role in anti-inflammatory effect in lipopolysaccharide-stimulated RAW 264.7 macrophages

  • Kim, Dong-Hee (Team of Product Development, Daegu Gyeongbuk Institute for Oriental Medicine Industry) ;
  • Moon, Yong-Sun (Dept. of Horticulture & Life Science, Yeungnam University) ;
  • Park, Tae-Soon (Team of Product Development, Daegu Gyeongbuk Institute for Oriental Medicine Industry) ;
  • Son, Jun-Ho (Team of Product Development, Daegu Gyeongbuk Institute for Oriental Medicine Industry)
  • 투고 : 2015.10.06
  • 심사 : 2015.12.02
  • 발행 : 2015.12.31

초록

Safflower (Carthamus tinctorius) seeds are wellknown traditional oriental medicines that have long been used for the remedies of blood stasis and bone formation in east Asia. In this study, ethyl acetate (EtOAc) was used for extraction of the main chemical compounds from C. tinctorius seeds. Four major compounds were identified, acacetin, cosmosiin, N-feruloyl serotonin and N-(p-coumaroyl) serotonin. Each compound was evaluated for its inhibitory activity against the inflammatory process of macrophages. All compounds significantly inhibited production of lipopolysaccharide (LPS)-stimulated nitric oxide (NO) and pro-inflammatory cytokines. The protein levels of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) were dramatically decreased by serotonins in a dose-dependent manner in LPS-stimulated RAW 264.7 macrophages. These results suggest that serotonin derivatives from safflower seeds may reduce inflammation-related diseases.

키워드

참고문헌

  1. Abdelrahman M, Sivarajah A, Thiemermann C (2005) Beneficial effects of PPAR-(ligands in ischemia-reperfusion injury, inflammation and shock. Cardiovasc Res 65:772-781 https://doi.org/10.1016/j.cardiores.2004.12.008
  2. Delgado AV, McManus AT, Chambers JP (2003) Production of tumor necrosis factor-alpha, interleukin 1-beta, interleukin 2, and interleukin 6 by rat leukocyte subpopulations after exposure to substance. Neuropeptides 37:355-361 https://doi.org/10.1016/j.npep.2003.09.005
  3. Feldman JM, Lee EM (1985) Serotonin content of foods: effect on urinary excretion of 5-hydroxyindoleacetic acid. Am J Clin Nutr 42:639-643 https://doi.org/10.1093/ajcn/42.4.639
  4. Han SY, Li HX, Ma X, Zhang K, Ma ZZ, Tu PF (2009) Protective effects of purified safflower extract on Myocardial ischemia in vivo and in vitro. Phytomedicine 16:694-702 https://doi.org/10.1016/j.phymed.2009.02.019
  5. Hewett JA, Roth RA (1993) Hepatic and extra hepatic pathobiology of bacterial lipopolysaccharides. Pharmacol Rev 45:382-411
  6. Kang KY, Park SK, Kim YS, Lee SB, Back KW (2009) Biosynthesis and biotechnological production of serotonin derivatives. Appl Microbiol Biotechnol 83:27-34 https://doi.org/10.1007/s00253-009-1956-1
  7. Kim DH, Hwang EY, Son JH (2013) Anti-inflammatory activity of Carthamus tinctorious seed extracts in Raw 264.7 cells. J Life science 23:55-62 https://doi.org/10.5352/JLS.2013.23.1.55
  8. Kim DH, Moon YS, An BJ, Son JH (2012) Potent anti-aging activity of Aruncus dioicus, a native plant of ulleung-do, south Korea, in CCD-986sk fibroblasts via suppression of matrix metalloproteinases. J Nat Med 66:631-636 https://doi.org/10.1007/s11418-012-0633-3
  9. Kim IH (1998) Carthamus tinctorius. In: Sinyakboncho. Insandongcheon press, Seoul, Korea, pp. 567-568
  10. Kubes P, McCafferty DM (2000) Nitric oxide and intestinal inflammation. Am J Med 109:150-158 https://doi.org/10.1016/S0002-9343(00)00480-0
  11. Li HX, Han SY, Wang XW, Ma X, Zhang K, Wang L, Ma ZZ, Tu PF (2009) Effect of the carthamins yellow from Carthamu stinctorius L. on hemorheolo-gical disorders of blood stasis in rats. Food and Chemical Toxicol 47:1797-1802 https://doi.org/10.1016/j.fct.2009.04.026
  12. Mandade R, Sreenivas SA, Wanare R (2012) Antiulcer screening of Carthamus tinctorius on volume and acidity of stimulated gastric secretion in rats. J Pharmacol Pharmacother 3:185-188
  13. Makarov SS (2000) NF-${\kappa}B$ as a therapeutic target in chronic inflammation: recent advances. Mol Med Today 6:441-448 https://doi.org/10.1016/S1357-4310(00)01814-1
  14. Palmer RMJ, Ashton DS, Moncada S (1988) Vascular endothelial cells synthesize nitric oxide from L-arginine. Nature 333:664-666 https://doi.org/10.1038/333664a0
  15. Roh JS, Han JY, Kim JH, Hwang JK (2004) Inhibitory effects of active compounds isolated from safflower (Carthamus tinctorius L.) seeds for melanogenesis. Biol Pharm Bull 27:1976-1978 https://doi.org/10.1248/bpb.27.1976
  16. Sakamura S, Terayama Y, Kawakatsu S, Ichihara A, Saito H (1978) Conjugated serotonins related to cathartic activity in safflower (Carthamus tinctorious L.) seeds. Agric Biol Chem 42:1805-1806 https://doi.org/10.1271/bbb1961.42.1805
  17. Sakamura S, Terayama Y, Kawakatsu S, Ichihara A, Saito H (1980) Conjugated serotonins and phenolic constituents in safflower seed (Carthamus tinctorius L.). Agric Biol Chem 44:2951-2954 https://doi.org/10.1271/bbb1961.44.2951
  18. Seo HJ, Kim JH, Kwak DY, Jeon SM, Ku SK, Lee JH, Moon KD, Choi MS (2000) The effects of safflower seed powder and its fraction on bone tissue in rib-fractured rats during the recovery. Kor J Nutr 33:411-420
  19. Schroder P, Abele C, Gohr P, Stuhlfauth-Roisch U, Grosse W (1999) Latest on enzymology of serotonin biosynthesis in walnut seeds. Adv Exp Med Biol 467:637-644 https://doi.org/10.1007/978-1-4615-4709-9_81
  20. Surh YJ, Na HK (2008) NF-${\kappa}B$ and Nrf2 as prime molecular targets for chemoprevention and cytoprotection with antiinflammatory and antioxidant phytochemicals. Genes Nutr 2:313-317 https://doi.org/10.1007/s12263-007-0063-0
  21. Tannenbaum H, Davis P, Russell AS, Atkinson MH, Maksymowych W, Huang SH, Bell M, Hawker GA, Juby A, Vanner S, Sibley J (1996) An evidence-based approach to prescribing NSAIDs in musculoskeletal disease: a Canadian consensus. Canadian NSAID Consensus Participants. Can Med Assoc J 155:77-88
  22. Watson WH, Zhao Y, Chawla RK (1999) S-adenosylmethionine attenuates the lipopolysaccharide-induced expression of the gene for tumor necrosis factor alpha. Biochem J 342:21-25 https://doi.org/10.1042/bj3420021
  23. Xie Q, Nathan C (1994) The high-output nitric oxide pathway: role and regulation. J Leukoc Biol 56:576-592 https://doi.org/10.1002/jlb.56.5.576