Effects of Samki-eum ($s\bar{a}nq\grave{i}-y\check{i}n$ ) on Freund's Complete Adjuvant-induced Arthritic Rats

Adjuvant 유발 관절염 랫트에 대한 삼기음의 효과

  • Choi, Eun-Sill (Department of Oriental Rehabiliation Medicine, College of Oriental Medicine, Daegu Hanny University) ;
  • Jang, Hong-Gyu (Department of Oriental Rehabiliation Medicine, College of Oriental Medicine, Daegu Hanny University) ;
  • Kwon, O-Gon (Department of Oriental Rehabiliation Medicine, College of Oriental Medicine, Daegu Hanny University) ;
  • Woo, Chang-Hoon (Department of Oriental Rehabiliation Medicine, College of Oriental Medicine, Daegu Hanny University) ;
  • An, Hee-Duk (Department of Oriental Rehabiliation Medicine, College of Oriental Medicine, Daegu Hanny University)
  • 최은실 (대구한의대학교 한의과대학 한방재활의학과교실) ;
  • 장홍규 (대구한의대학교 한의과대학 한방재활의학과교실) ;
  • 권오곤 (대구한의대학교 한의과대학 한방재활의학과교실) ;
  • 우창훈 (대구한의대학교 한의과대학 한방재활의학과교실) ;
  • 안희덕 (대구한의대학교 한의과대학 한방재활의학과교실)
  • Published : 2013.07.31

Abstract

Objectives The object of this study was to observe the favorable anti-arthritic effects of Samki-eum ($s\bar{a}nq\grave{i}-y\check{i}n$) on Freund's complete adjuvant (FCA)-induced arthritic Wistar rats. Methods Rheumatoid arthritis was induced by intradermal injection of FCA, and 300, 150 or 750 mg/kg of Samki-eum ($s\bar{a}nq\grave{i}-y\check{i}n$) were orally administered once a day for 14 days from 14 days after FCA treatments, and 15 mg/kg of dexamethasone was intraperitoneally administered as reference drug in this experiment. All rats were sacrificed at 14 days after continuous oral treatment of Samki-eum ($s\bar{a}nq\grave{i}-y\check{i}n$) or intraperitoneal administration of dexamethasone, and changes on the body weight, knee circumferences, gross arthritis score, inflammatory tissue prostaglandin (PG) $E_2$ levels were monitored with cartilage collagen components and glucosaminoglycans compositions - chondroitin sulphate, heparan sulphate and hyaluronic acid in the present study. Results As results of FCA treatment, classic rheumatoid arthritis featuring dramatical decreases on the body weights, cartilage collagen contents and bone glucosaminoglycans-chondroitin sulphate, heparan sulphate and hyaluronic acid contents, with increases on the knee circumferences, gross arthritis scores and inflammatory tissue $PGE_2$ levels. However, these changes from FCA-induced rheumatoid arthritis were clearly reduced by treatment of dexamethasone and both two different dosages of Samki-eum ($s\bar{a}nq\grave{i}-y\check{i}n$) 300 and 150 mg/kg in the present study. Although FCA-induced arthritis were more favorably inhibited by treatment of dexamethasone 15 mg/kg as compared with Samki-eum ($s\bar{a}nq\grave{i}-y\check{i}n$) 300 mg/kg, marked decreases of body weights were detected in dexamethasone 15 mg/kg treated rats, and Samki-eum ($s\bar{a}nq\grave{i}-y\check{i}n$) 300 mg/kg showed similar preserve effects on the cartilage glucosaminoglycan compositions in this study. Conclusions The results obtained in this study suggest that over 300 and 150 mg/kg of Samki-eum ($s\bar{a}nq\grave{i}-y\check{i}n$) showed favorable anti-arthritic effects on the FCA-induced arthritis mediated by suppression of $PGE_2$, a inflammatory mediator. However, detail mechanism studies should be conduced in future with the screening of the biological active compounds in this herb. Although overall anti-inflammatory effects Samki-eum ($s\bar{a}nq\grave{i}-y\check{i}n$) 300 mg/kg were lowered than those of dexamethasone 15 mg/kg treated rats, Samki-eum ($s\bar{a}nq\grave{i}-y\check{i}n$) 300 mg/kg treated rats showed similar preserve effects on the cartilage glucosaminoglycan compositions in this experiment.

Keywords

References

  1. Lipsky PE, Braunwald E, Fauci A, Kasper D, Hauser S, longo D, Jameson J. Harrisons's principles of internal medicine. 18th ed. New York:Mc Graw Hill. 2005:1968-77.
  2. Visser H, le Cessie S, Vos K, Breedveld FC, Hazes JM. How to diagnose rheumatoid arthritis early: a prediction model for persistent(erosive) arthritis. Arthritis Rheum 2002;46:357-65. https://doi.org/10.1002/art.10117
  3. 한방재활의학과학회. 한방재활의학. 3판. 서울:군자출판사. 2011.
  4. 張介賓. 景岳全書. 서울:정담. 1999.
  5. 黃道淵. 方藥合編. 서울:영림사. 2003.
  6. 정창영, 성윤희, 김성은, 김창주, 한승. 쥐 BV2 미세아교세포에서 cyclooxygenase-2와 유도 산화질소 합성효소의 발현에 미치는 숙지황 추출물의 효과. 동의생리병리학회지. 2006;20(4):1051-6.
  7. 이희조, 황귀서, 김경준. 지단백산화에 따른 대식세포 활성에 미치는 三氣飮의 영향. 한방안이비인후피부과학회지. 2006;19(2):108-17.
  8. 이경무, 정수현, 김순중, 서일복. 三氣飮이 흰쥐의 monosodium iodoacetate 유발 골관절염에 미치는 영향. 한방재활의학과학회지. 2008;18(2):17-31.
  9. 신강우, 이철완. 三氣飮去附子가 adjuvant 유발 관절염에 미치는 실험적 비교연구. 한방재활의학과학회지. 1995;5(1):163-81.
  10. 김순중, 이철완. 三氣飮 및 三氣飮去附子가 adjuvant 관절염 유발시 활성산소에 미치는 영향. 한방재활의학과학회지. 1997;7(2):1-45.
  11. National research concill of the national academies. Washington, DC.:National academies press. 2011.
  12. Ramprasath VR, Shanthi P, Sachdanandam P. Therapeutic effects of Semecarpus anacardium Linn. nut milk extract on the changes associated with collagen and glycosaminoglycan metabolism in adjuvant arthritic Wistar rats. Chem Biol Interact. 2006;162:43-52. https://doi.org/10.1016/j.cbi.2006.05.003
  13. Kim HD, Cho HR, Moon SB, Shin HD, Yang KJ, Park BR, Jang HJ, Lim LS, Lee HS, Ku SK. Effect of Exopolymers from Aureobasidum pullulans on formalin-induced chronic paw inflammation in mice. J Microbiol Biotechnol. 2006;16:1954-60.
  14. Bamgbose SO, Noamesi BK. Studies on cryptolepine. II: inhibition of carrageenan induced oedema by cryptolepine. Planta Med. 1981;41:392-6. https://doi.org/10.1055/s-2007-971733
  15. Hatori M, Ohki K, Hirano S, Yang XP, Kuboki H, Abe C. Effects of a casein hydrolysate prepared from Aspergillus oryzae protease on adjuvant arthritis in rats. Biosci Biotechnol Biochem. 2008;72:1983-91. https://doi.org/10.1271/bbb.70792
  16. Chen Q. Method of Chinese medicine pharmacology. Beijing:Chinese People Health Press. 1996.
  17. Leach AA. Notes on a modification of the Neuman and Logan method for the determination of the hydroxyproline. Biochem J. 1960;74:70-1. https://doi.org/10.1042/bj0740070
  18. Neuman RE, Logan MA. The determination of collagen and elastin in tissues. J Biol Chem. 1950;186:549-56.
  19. Neuman RE, Logan MA. The determination of hydroxyproline. J Biol Chem. 1950;184:299-306.
  20. Homer KA, Denbow L, Beighton D. Spectrophotometric method for the assay of glycosaminoglycans and glycosaminoglycan-depolymerizing enzymes. Anal Biochem. 1993;214:435-41. https://doi.org/10.1006/abio.1993.1520
  21. Levene A. Pathological factors influencing excision of tumours in the head and neck. Part I. Clin Otalary. 1981;6:145-51. https://doi.org/10.1111/j.1365-2273.1981.tb01800.x
  22. Ludbrook J. Update: microcomputer statistics packages. A personal view. Clin Exp Pharmacol Physiol. 1997;24:294-6. https://doi.org/10.1111/j.1440-1681.1997.tb01823.x
  23. 박용욱, 박재홍, 배윤상, 김태환, 전재범, 정성수, 배상철, 김성윤, 유대현. HBsAg 양성인 류마티스 관절염 환자와 HBsAg 음성인 류마티스 관절염 환자의 methotrexate에 대한 간독성의 비교. 대한류마티스학회지. 2001;8(4):227-35.
  24. Zhou H, Wu D, Ma L. Clinical analyses of severe harmful effects with low dose methrotrexate in short time. Chinese J Rhematol. 2002;4:135-7.
  25. 서영일. 류마티스 관절염의 새로 개발된 치료제. 대한내과학회지. 2009;76(1):12-7.
  26. Robinson WH, Genoverse MC, Moreland LW. Demyelinating and neurologic events reported in association with tumor necrosis factor alpha antagonists improve rheumatoid arthritis but exacerbate multiple sclerosis? Arthritis Rheum. 2001;44:1977-83. https://doi.org/10.1002/1529-0131(200109)44:9<1977::AID-ART345>3.0.CO;2-6
  27. Reddy GK, Dhar SC. Metabolism of glycosaminoglycans in tissues of adjuvant arthritic rat. Mol Cell Biochem. 1991;106:117-24.
  28. Seed MP, Gardner CR. The modulation of intra-articular inflammation, cartilage matrix and bone loss in mono-articular arthritis induced by heat-killed Mycobacterium tuberculosis. Inflammopharmacology. 2005;12:551-67. https://doi.org/10.1163/156856005774382607
  29. Okumura T, Murata Y, Taniguchi K, Murase A, Nii A. Effects of the selective EP4 antagonist, CJ-023,423 on chronic inflammation and bone destruction in rat adjuvant-induced arthritis. J Pharm Pharmacol. 2008;60:723-30. https://doi.org/10.1211/jpp.60.6.0007
  30. Yoshikawa T, Tanaka H, Kondo M. Lipid peroxidation in rat adjuvant arthritis and its inhibition by indomethacin. J Appl Biochem. 1983;5:382-7.
  31. Yoshikawa T, Tanaka H, Kondo M. Effect of vitamin E on adjuvant arthritis in rats. Biochem Med. 1983;29:227-34. https://doi.org/10.1016/0006-2944(83)90043-1
  32. Kang SY, Yoon SY, Roh DH, Jeon MJ, Seo HS, Uh DK, Kwon YB, Kim HW, Han HJ, Lee HJ, Lee JH. The anti-arthritic effect of ursolic acid on zymosan-induced acute inflammation and adjuvant-induced chronic arthritis models. J Pharm Pharmacol. 2008;60:1347-54. https://doi.org/10.1211/jpp.60.10.0011
  33. Gupta AK, Chow M. Prednicarbate (Dermatop): profile of a corticosteroid. J Cutan Med Surg. 2004;8:244-7. https://doi.org/10.1007/s10227-004-0120-x
  34. Chi YM, Nakamura M, Zhao AY, Yoshizawa T, Yan WM, Hashimoto F, Kinjo J, Nohara T, Sakurada S. Anti-inflammatory activity of 4, 4'-dihydroxy-alpha-truxillic acid. Biol Pharm Bull. 2006;29:489-93. https://doi.org/10.1248/bpb.29.489
  35. Ganguly S, Mula S, Chattopadhyay S, Chatterjee M. An ethanol extract of Piper betle Linn. mediates its anti-inflammatory activity via down-regulation of nitric oxide. J Pharm Pharmacol. 2007;59:711-8. https://doi.org/10.1211/jpp.59.5.0012
  36. Zaringhalam J, Manaheji H, Mghsoodi N, Farokhi B, Mirzaiee V. Spinal mu-opioid receptor expression and hyperalgesia with dexamethasone in chronic adjuvant-induced arthritis in rats. Clin Exp Pharmacol Physiol. 2008;35:1309-15. https://doi.org/10.1111/j.1440-1681.2008.05009.x
  37. Yu F, Yu F, Li R, Wang R. Inhibitory effects of the Gentiana macrophylla (Gentianaceae) extract on rheumatoid arthritis of rats. J Ethnopharmacol. 2004;95:77-81. https://doi.org/10.1016/j.jep.2004.06.025
  38. Dubois RN, Abramson SB, Crofford L, Gupta RA, Simon LS, Van De Putte LB, Lipsky PE. Cyclooxygenase in biology and disease. FASEB J. 1998;12:1063-73.
  39. Fogel-Petrovic M, Long JA, Knight DA, Thompson PJ, Upham JW. Activated human dendritic cells express inducible cyclo-oxygenase and synthesize prostaglandin E2 but not prostaglandin D2. Immunol Cell Biol. 2004;82: 47-54. https://doi.org/10.1111/j.1440-1711.2004.01213.x
  40. Poole AR, Witter J, Roberts N, Piccolo F, Brandt R, Paquin J, Baron M. Inflammation and cartilage metabolism in rheumatoid arthritis. Studies of the blood markers hyaluronic acid, orosomucoid, and keratan sulfate. Arthritis Rheum. 1990;33:790-9. https://doi.org/10.1002/art.1780330605
  41. Haraoui B, Thonar EJ, Martel-Pelletier J, Goulet JR, Raynauld JP, Ouellet M, Pelletier JP. Serum keratan sulfate levels in rheumatoid arthritis: inverse correlation with radiographic staging. J Rheumatol. 1994;21:813-7.
  42. Emlen W, Niebur J, Flanders G, Rutledge J. Measurement of serum hyaluronic acid in patients with rheumatoid arthritis: correlation with disease activity. J Rheumatol. 1996;23:974-8.