- P-ISSN 1010-0695
- E-ISSN 2288-3339
Objectives: The purpose of this study is to investigate changes of the marker compounds and anti-inflammatory effect of Gamisoyo-san decoction (GMSYS) depending on storage temperature and periods. Methods: GMSYS was stored at room temperature or refrigeration for 12 months. According to storage temperature and periods, pH and sugar content of GMSYS were measured. To determine the marker compounds of GMSYS, high-performance liquid chromatography analysis was performed. To estimate the anti-inflammatory effect of GMSYS, LPS-induced pro-inflammatory mediators and cytokines were measured in RAW 264.7 cells. Results: There was no change in pH and sugar content depending on storage temperature and periods of GMSYS. The contents of gallic acid and mangiferin in both of room temperature and refrigerated decoctions reduced with increasing storage periods. Chlorogenic acid was time-dependently decreased in case of stored at room temperature. GMSYS significantly inhibited the LPS-induced production of nitric oxide, prostaglandin E2 (PGE2) and IL-6 in RAW 264.7 cells. These effects equally maintained up to 3 months at both of room temperature and refrigeration. Since 4 months, the inhibitory effect of GMSYS on LPS-induced PGE2 production was time-dependently reduced, and the decrease in PGE2 inhibitory effect of decoction stored at refrigeration was lower than that of stored at room temperature. Conclusions: Our results indicate that the anti-inflammatory effect of GMSYS are maintained up to 12 months, but it shows optimal efficacy up to 3 months. It is recommended to store in a refrigeration for short periods since some components decrease as storage periods becomes longer.
The co-textbook publishing committee of Korean Medicine College. Formula Science. Seoul: Younglimsa. 2009.
Seo CS, Shin HK, Kim JH, Shin KS. Changes of Principal Components and Microbial Population in Pyungwi-san Decoction According to the Preservation Temperature and Period. J Korean Oriental Med. 2011;32(5):41-9.
Ha H, Shin IS, Lim HS, Jeon WY, Kim JH, Seo CS, Shin HK. Changes in Anti-inflammatory Effect of Pyungwi-san Decoction According to the Preservation Temperature and Period. Formula Science. 2012;20(2):29-35.
Seo CS, Kim JH, Lim SH, Shin HK. Establishment of Shelf-Life of Ssanghwa-tang by Long-term Storage Test. Kor J Pharmacogn. 2012;43(3):257-64.
Seo CS, Kim JH, Kim SS, Lim SH, Shin HK. Evaluation of Shelf-life of Bojungikgi-tang by Long-term Storage Test. Kor J Pharmacogn. 2013;44(2):200-8.
Jin SE, Kin OS, Shin HK, Jeong SJ. Comparative Study on Biological Activities of Gwakhyangjeonggi-san Decoction According to the Preservation Periods. J Korean Med. 2014;35(3):60-9.
Jin SE, Kim OS, Seo CS, Shin HK, Jeong SJ. Comparative study on stability and efficacy of Banhasasim-tang decoction depending on the preservation temperature and periods. J Korean Med. 2016;37(1):21-33.
Yoo SR, Ha H, Lee NR, Shin HK, Seo CS. A Study on Change of Marker Compounds and Biological Activity in Chungsimyeonja-eum Decoction Depending on A Storage Temperature and Periods. Kor J Herbol. 2017;32(4):25-32.
Park IH, Kim YH, Choi SH, Yu SN, Kim SH, Ahn SC, Cho SI, Lee I. Effect of Preservation Conditions on the Stability of Samul-tang Decoctions. J Life Sci. 2015;25(10):1124-31.
Do HJ, Shim YS, Lee JH, Ahn YJ, Ha IH, Lee YJ, et al. Stability of Danggwisu-san (Dangguixu-san) Water Extract, a Herbal Medicine, Under Various Storage Conditions. Journal of Oriental Rehabilitation Medicine. 2016;26(4):1-8.
Jin SM. Taepyunghyeminhwajekukbang. Inminweeseng Publications. 1985;308.
Sim TK, Jung IC, Lee SR. The Effect of Gami soyo-san(Jiaweixiaoyaosan) on Serotonin Metabolism. Journal of Oriental Neuropsychiatry. 2011;22(1):37-51.
Lee SL, Lee IS, Soh KS. Effects of Gamisoyosan(Jiaweixiaoyaosan 加味逍遙散) on Type II Collagen-Induced Arthritis. J Oriental Rehab Med. 2001;12(4):167-76.
Jin SE, Kim OS, Yoo SR, Seo CS, Kim Y, Shin HK, et al. Anti-inflammatory effect and action mechanisms of traditional herbal formula Gamisoyo-san in RAW 264.7 macrophages. BMC Complement Altern Med. 2016;16:219. doi: 10.1186/s12906-016-1197-7.
Choi HM, Kim SJ, Kim IS, Lee JB, Kim JB, Moon SO, et al. Evaluation on Anti-oxidant Activity and Anti-inflammatory Effects for the New Formulation of Gamisoyosan. Kor J Herbol. 2016;31(6):1-9.
Willoughby DA. Human arthritis applied to animal models. Towards a better therapy. Ann Rheum Dis. 1975;34:471-8.
Lee ES, Ju HK, Moon TC, Lee E, Jahng Y, Lee SH, et al. Inhibition of nitric oxide and tumor necrosis factor <TEX>${\alpha}$</TEX> (TNF-<TEX>${\alpha}$</TEX>) production by propenone compound through blockade of nuclear factor (NF)-<TEX>${\kappa}B$</TEX> activation in cultured murine macrophages. Biol Pharm Bull. 2004;27:617-20.
Wink DA. Chemical biology of nitric oxide: Insights into regulatory, cytotoxic, and cytoprotective mechanisms of nitric oxide. Free Radic Biol Med. 1998;25(4-5):434-56.
Ryu JH, Ahn H, Kim JY, Kim YK. Inhibitory activity of plant extracts on nitric oxide synthesis in LPS-activated macrophages. Phytother Res. 2003;17(5):485-9.
Funk CD, Fitzgerald GA. Human platelet, erythroleukemia cell prostaglandin G, H synthase: cDNA cloning, expression, and gene chromosomal assignment. FASEB J. 1991;5:2304-12.
Bishop-Bailey D, Calatayud S, Warner TD, Hla T, Michell A. Prostaglandins and the regulation of tumor growth. J Environ Pathol Tox Oncol. 2002;21:93-101.
Feldmann M. Role of cytokines in rheumatoid arthritis. Annu Rev Immunol. 1996;14:397-440.
Mann JR, Backlund MG, DuBois RN. Mechanism of disease: Inflammatory mediators and cancer prevention. Nat Clin Pract Oncol. 2005;2:202-10.
Guzik TJ, Korbut R, Adamek-Guzik T. Nitric oxide and superoxide in inflammation and immune regulation. J Physiol Phamacol. 2003;43:469-87.
Chiu CS, Deng JS, Chang HY, Chen YC, Lee MM, Hou WC, et al. Antioxidant and anti-inflammatory properties of Taiwanese yam (Dioscorea japonica Thunb. var. pseudojaponica (Hayata) Yamam.) and its reference compounds. Food Chem. 2013;141:1087-96.
Hwang SJ, Kim YW, Park Y, Lee HJ, Kim KW. Anti-inflammatory effects of chlorogenic acid in lipopolysaccharide-stimulated RAW 264.7 cells. Inflamm Res. 2014;63:81-90.
Garrido G, Delgado R, Lemus Y, Rodriguez J, Garcia D, Nunez-Selles AJ. Protection against septic shock and suppression of tumor necrosis factor alpha and nitric oxide production on macrophages and microglia by a standard aqueous extract of Mangifera indica L. (VIMANG). Role of mangiferin isolated from the extract. Pharmacol Res. 2004;50:165-72.
Shi Q, Cao J, Fang L, Zhao H, Liu Z, Ran J, et al. Geniposide suppresses LPS-induced nitric oxide, <TEX>$PGE_2$</TEX> and inflammatory cytokine by downregulating NF-kB, MAPK and AP-1 signaling pathways in macrophages. Int Immunopharmacol. 2014;20:298-306.
Wang QS, Gao T, Cui YL, Gao LN, Jiang HL. Comparative studies of paeoniflorin and albiflorin from Paeonia lactiflora on anti-inflammatory activities. Pharm Biol. 2014;52(9):1189-95.
Jeong HW, Hsu KC, Lee JW, Ham M, Huh JY, Shin HJ, et al. Berberine suppresses proinflammatory responses through AMPK activation in macrophages. Am J Physiol Endocrinol Metab. 2009;296:E955-64.
Guan Y, Li FF, Hong L, Yan XF, Tan GL, He JS, et al. Protective effects of liquiritin apioside on cigarette smoke-induced lung epithelial cell injury. Fundam Clin Pharmacol. 2012;26(4):473-83.
Rim HK, Cho W, Sung SH, Lee KT. Nodakenin suppresses lipopolysaccharide-induced inflammatory responses in macrophage cells by inhibiting tumor necrosis factor receptor-associated factor 6 and nuclear factor-kB pathways and protects mice from lethal endotoxin shock. J Pharmacol Exp Ther. 2012;342:654-64.
Fu Y, Zhou E, Wei Z, Liang D, Wang W, Wang T, et al. Glycyrrhizin inhibits the inflammatory response in mouse mammary epithelial cells and a mouse mastitis model. FEBS J. 2014;281:2543-57.