Anti-Arthritic Activity of Combination of <i>Caesalpinia sappan</i> and <i>Zingiber officinale</p> Extracts in Complete Freund’s Adjuvant- Induced Arthritic in Rats

http://www.doi.org/10.26538/tjnpr/v7i11.19

Authors

  • Tukiran Tukiran Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Negeri Surabaya, Surabaya, Indonesia
  • Nadiah A. Salma Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Negeri Surabaya, Surabaya, Indonesia
  • Suyatno Sutoyo Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Negeri Surabaya, Surabaya, Indonesia
  • Fauzia I. Sabila Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Negeri Surabaya, Surabaya, Indonesia

Abstract

Several plant species, including sappan and red ginger, have been studied to treat inflammation. Each species has been tested for anti-arthritis, but a combination of the two species has never been done. This study was conducted to test the anti-arthritis potential of a combination of ethanol extract of sappan wood and red ginger using a rat model of Complete Freund's Adjuvant-induced rheumatism. The study involved several percentages of inhibition of rat paw edema volume (%), arthritis index, histopathological profile, and haematological evaluation. The test formula prepared included sappan wood single extract (ES), red ginger single extract (ERG), comparison of the combination of two extracts at doses F1 (1 ES: 1 ERG), F2 (2 ES: 1 ERG), and F3 (1 ES: 2 ERG). The results showed that the F2 formula had the best anti-arthritis effect with an inhibition percentage of rat paw edema volume of 86.72% by showing relatively mild inflammatory cell infiltration, the formation of connective tissue through histopathological observations of rat foot tissue. Haematological observations of platelet increase were highest in group F2 which functions to defend the body from toxic substances. There was no significant difference in the rat haematological parameter in each treatment group (p>0.05).

References

Calabresi E, Petrelli F, Bonifacio AF, Puxeddu I, Alunno A. One year in review 2018: pathogenesis of rheumatoid arthritis. Clin Exp Rheumatol. 2018; 36(2):175–84.

Mendoza-Vázquez G, Rocha-Muñoz AD. Arthritis reumatoide y dislipidemias. El Residente. 2013; 8(1):12–22.

Zhu L, Chen T, Chang X. Salidroside ameliorates arthritisinduced brain cognition deficits by regulating Rho/ROCK/NFkappaB pathway. J Neuropharm. 2016; 103:134–42. Doi: 10.1016/j.neuropharm.2015.12.007.

Campbell IK, Piccoli DS, Hamilton JA. Stimulation of human chondrocyte prostaglandin E2 production by recombinant human interleukin-1 and tumour necrosis factor. Biochim Biophys Acta. 1990; 1051(3):310–18. Doi: 10.1016/0167-4889(90)90140-9.

Jeong JH, Moon SJ, Jhun JY, Yang EJ, Cho ML, Min JK. Eupatilin exerts antinociceptive and chondroprotective properties in a rat model of osteoarthritis by downregulating oxidative damage and catabolic activity in chondrocytes. PLoS One. 2015; 10(6):e0130882. Doi: 10.1371/journal.pone.0130882.

Chimenti MS, Triggianese P, Conigliaro P, Candi E, Melino G, Perricone R. The interplay between inflammation and metabolism in rheumatoid arthritis. Cell Death Dis. 2015; 6(9):e1887. Doi: 10.1038/cddis.2015.246.

Das C, Bose A, Das D. Ayurvedic Balarista ameliorate antiarthritic activity in adjuvant induced arthritic rats by inhibiting proinflammatory cytokines and oxidative stress. J Tradit Complement Med. 2021; 11(3):228–37. Doi: 10.1016/j.jtcme.2020.04.006.

McInnes IB, Schett G. Pathogenetic insights from the treatment of rheumatoid arthritis. Lancet. 2017; 389(10086):2328–37. Doi: 10.1016/S0140-6736(17)31472-1.

Laine L. The gastrointestinal effects of nonselective NSAIDs and COX-2-selective inhibitors. Semin Arthritis Rheum. 2002; 32(3 Suppl 1):25–32. Doi: 10.1053/sarh.2002.37217.

Ravindran V, Rachapalli S, Choy EH. Safety of medium- to long-term glucocorticoid therapy in rheumatoid arthritis: a meta-analysis. Rheumatology (Oxford). 2009; 48(7):807–11. Doi: 10.1093/rheumatology/kep096.

Jain S, Vaidya A, Gupta PK, Rosenholm JM, Bansal KK. Antiarthritic activities of herbal isolates: a comprehensive review. Coatings. 2021; 11(11):1329. Doi: 10.3390/coatings11111329.

Jung EG, Han KI, Hwang SG, Kwon HJ, Patnaik BB, Kim YH, Han MD. Brazilin isolated from Caesalpinia sappan L. inhibits rheumatoid arthritis activity in a type-II collagen induced arthritis mouse model. BMC Complement Altern. Med. 2016; 15(124):1–11. Doi: 10.1186/s12906-015-0648-x.

Ezzat SM, Ezzat MI, Okba MM, Menze ET, Abdel-Naim AB. The hidden mechanism beyond ginger (Zingiber officinale Rosc.) potent in vivo and in vitro anti-inflammatory activity. J. Ethnopharmacol. 2018; 214:113–23. Doi: 10.1016/j.jep.2017.12.019.

Laksmiani NPL, Leliqia NPE, Armita PMN, Nyoman Arijana IGK, Yoga Saputra AAB, Prananingtyas KI. In-silico and in-vitro studies of antioxidant and sun protection activities of sappan wood (Caesalpinia sappan L.). Trop J Nat Prod Res. 2020; 4(12):1072-1080. doi.org/10.26538/tjnpr/v4i12.8.

Chu MJ, Wang YZ, Itagaki K, Ma HX, Xin P, Zhou XG, Chen GY, Li S, Sun SQ. Identification of active compounds from Caesalpinia sappan L. extracts suppressing IL-6 production in RAW 264.7 cells by PLS. J. Ethnopharmacol. 2013; 148(1):37–44. Doi: 10.1016/j.jep.2013.03.050.

Min BS, Cuong TD, Hung TM, Min BK, Shin BS, Woo MH. Compounds from the heartwood of Caesalpinia sappan and their anti-inflammatory activity. Bioorganic Med. Chem Lett. 2012; 22(24):7436–9. Doi: 10.1016/j.bmcl.2012.10.055.

Jung EG, Han KI, Kwon HJ, Patnaik BB, Kim WJ, Hur GM, Nam KW, Han MD. Anti-inflammatory activity of sappanchalcone isolated from Caesalpinia sappan L. in a collagen-induced arthritis mouse model. Arch. Pharm. Res. 2015; 38(6):973–83. Doi: 10.1007/s12272-015-0557-z.

Yan Y, Chen YC, Lin YH, Guo J, Niu ZR, Wang SB, Fang LH, Du GH. Brazilin isolated from the heartwood of Caesalpinia sappan L induces endothelium-dependent and independent relaxation of rat aortic rings. Acta Pharmacol. Sin. 2015; 56(1):1318–26. Doi: 10.1038/aps.2015.113.

Tao LY, Li YJ, Zhang JY. Brazilein, a compound isolated from Caesalpinia sappan Linn., induced growth inhibition in breast cancer cells via involvement of GSK-3β/β-Catenin/cyclin D1 pathway. Chem. Biol. Interact. 2013; 206(1):1–5. Doi: 10.1016/j.cbi.2013.07.015.

Kim KJ, Yoon KY, Yoon HS, Oh SR, Lee BY. Brazilein suppresses inflammation through inactivation of IRAK4-NF-κB pathway in LPS-induced raw264.7 macrophage cells. Int. J. Mol. Sci. 2015; 16(11):27589–98. Doi: 10.3390/ijms161126048.

Mbaveng A, Kuete V. Zingiber officinale. In: medicinal spices and vegetables from Africa. Amsterdam: Elsevier; 2017. 627–39. Doi: 10.1002/ptr.2142.

Wahid RAH, Purwaningsih O, Pamungkas PB. Phytochemical profiling and antioxidant activities of red ginger (Zingiber officinale var. rubrum) cultivated eco-farming. Trop J Nat Prod Res. 2023; 7(9):3968-73 Doi: 10.26538/tjnpr/v7i9.18.

Ahmad B, Rehman MU, Amin I, Arif A, Rasool S, Bhat SA, Afzal I, Hussain I, Bilal S, Mir MUR. A review on pharmacological properties of zingerone (4-(4-Hydroxy-3-methoxyphenyl)-2-butanone). Sci. World J. 2015; 2015(6):1–6.

Barik CS, Kanungo SK, Tripathy NK, Panda JR, Padhi M. A review on therapeutic potential of polyherbal formulations. Int J Pharm Sci Drug Res. 2015; 7(3):211-28. Doi: http://www.ijpsdr.com/index.php/ijpsdr/article/view/414.

Patel SS, Shah PV. Evaluation of anti-inflammatory potential of the multidrug herbomineral formulation in male Wistar rats against rheumatoid arthritis. J Ayurveda Integr Med. 2013; 4(2):86–93.

Klopfleisch R. Multiparametric and semiquantitative scoring systems for the evaluation of mouse model histopathology - a systematic review. BMC Vet Res. 2013; 9(1):123. Doi: 10.4103/0975-9476.113869.

Sharma H, Chauhan P, Singh S. Evaluation of the antiarthritic activity of Cinnamomum cassia bark extract in experimental models. Integr Med Res. 2018; 7(4):366–73. Doi: 10.1016/j.biopha.2016.12.027.

Baisa S, Abrolb N, Prashara Y, Kumarib R. Modulatory effect of standardized amentoflavone isolated from Juniperus communis L. agianst Freund's adjuvant induced arthritis in rats (histopathological and X Ray anaysis). Biomed. Pharmacother. 2017; 86:368–73. Doi: 10.1186/1746-6148-9-123.

Nagakura Y, Okada M, Kohara A, Kiso T, Toya T, Iwai A, Wanibuchi F, Yamaguchi T. Allodynia and hyperalgesia in adjuvant-induced arthritic rats: time course of progression and efficacy of analgesics. J Pharmacol Exp Ther. 2003; 306(2):490–7. Doi: 10.1124/jpet.103.050781.

Sharma H, Chauhan P, Singh S. Evaluation of the anti-arthritic activity of Cinnamomum cassia bark extract in experimental models, Integr Med Res. 2018; 7:366–73. Doi: 10.1016/j.imr.2018.08.002.

Woolley DE. The mast cell in inflammatory arthritis. N Engl J Med. 2003; 348(17):1709–11. Doi: 10.1056/NEJMcibr023206.

Smit F. Pichrorhiza scrophulariiflora from traditional use to immunomodulary. Utrecht: Rijksuniversiteit Urtecht; 2000.

Hirohata S, Sakakibara J. Synovial histopathology in early rheumatoid arthritis. Arthritis Res. 2000; 1(Suppl 1):S38. Doi: 10.1186/ar52.

Parham P. The immune system. II. New York: Garland Science, Tylor & Francis Group; 2005.

Raghavendra V, Tanga FY, DeLeo JA. Complete Freunds adjuvant-induced peripheral inflammation evokes glial activation and proinflammatory cytokine expression in the CNS. Eur J Neurosci. 2004; 20(2):467–73. Doi: 10.1111/j.1460-9568.2004.03514.x.

Barik CS, Kanungo SK, Tripathy NK, Panda J, Pandhi M. Antibacterial study of polyherbal therapeutic agents used in respiratory diseases. World J Pharm. Res. 2015; 5(1):1144–52.

Price SA, Wilson LM. Patofisiologi, konsep klinis proses-proses penyakit, Jilid 1, EdisiVI, diterjemahkan oleh Brahm U. Pendit, Huriawati Hartanto, Pita Wulansari, Dewi Asih Mahanani. Jakarta: Buku Kedokteran ECG, 2006; 72–3.

Fitria L, Sarto M. Profil hematologi tikus (Rattus norvegicus Berkenhout, 1769) galur wistar jantan dan betina umur 4, 6, dan 8 minggu. Biogenesis. 2014; 2(2):94–100. Doi: 10.24252/bio.v2i2.473.

Thomas C, Lumb AB. Physiology of haemoglobin. Continuing education in anaesth critic care pain. 2012; 12(5):251–6. Doi: 10.1093/bjaceaccp/mks025.

Holinstat M. Normal platelet function. Cancer Metastasis Rev. 2017; 36(2):195–8. Doi: 10.1007/s10555-017-9677-x.

Silitonga M, Restuati M, Silitonga PM. The Benefits of ethanolic extract of Plectranthus amboinicus Lour Spreng on rats hematology profile that provided with Rhodamine-B. Environ. Earth Sci. 2018; 187:012028. Doi: 10.1088/1755-1315/187/1/012028.

Idang EO, Yemitan O, Ogbuagu EO, Yemitan OK, C Mbagwu HO, Udom GJ, Udobang JA. Toxicological assessment of Zingiber officinale Roscoe (ginger) root oil extracts in albino rats. Toxicol Digest. 2019; 4(1):108–19.

Martina SJ, Ramar LAP, Silaban MRI, Luthfi M, Govindan PAP. Antiplatelet effectivity between aspirin with honey on cardiovascular disease based on the bleeding time taken on mice. Open Access Maced. J. Med. Sci. 2019; 7(20):3416–20. Doi: 10.3889/oamjms.2019.431.

Published

2023-12-01

How to Cite

Tukiran, T., Salma, N. A., Sutoyo, S., & Sabila, F. I. (2023). Anti-Arthritic Activity of Combination of <i>Caesalpinia sappan</i> and <i>Zingiber officinale</p> Extracts in Complete Freund’s Adjuvant- Induced Arthritic in Rats: http://www.doi.org/10.26538/tjnpr/v7i11.19. Tropical Journal of Natural Product Research (TJNPR), 7(11), 5164–5171. Retrieved from https://tjnpr.org/index.php/home/article/view/3015