ERDOSTEINE: AN EFFECTIVE ANTIOXIDANT FOR PROTECTING COMPLETE FREUND’S ADJUVANT INDUCED ARTHRITIS IN RATS
DOI:
https://doi.org/10.22159/ajpcr.2021.v14i10.42365Keywords:
Erdosteine, Artharitis, CFA, MethotrexateAbstract
Objective: The objective of this study was to evaluate the protective effect of Erdosteine on complete freund’s adjuvant (CFA) induced arthritic rats.
Methods: Wistar Albino rats of 100–250 g were divided into five groups (n=6) and administered with 0.1 ml of CFA subcutaneously into the left hind paw except the negative control group. The standard group received methotrexate (MTX) 0.075 mg/kg body weight orally. Besides, the test groups received Erdosteine orally at a dose 10 mg/kg and 20 mg/kg bodyweight for 12 days. The changes in body weight, paw volume, hematological parameters, radiographical, and histological findings were the indicators to evaluate the efficacy of the test product.
Discussion: Significant change in the body weight, paw volume, radiographical, hematological, and histological parameters were observed which supports the remarkable reduction of the arthritic development in the standard and test groups compared to the untreated group. However, the test group (Erdosteine) with the dose 20 mg/kg shows to be more potent than the test group (Erdosteine) with a dose 10 mg/kg and the standard group (MTX) to reduce the arthritic effect.
Results: The test group with 20 mg/kg Erdosteine showed much better outcome than the standard group at significant (p<0.05). Therefore, Erdosteine acting as an anti-inflammatory and anti-oxidant is effective at a dose 20 mg/kg in treating the progression of rheumatoid arthritis in rats.
Downloads
References
Ren K, Dusad A, Dong R, Quan L. Albumin as a delivery carrier for rheumatoid arthritis. J Nanomed Nanotechol 2013;4:176.
Roger W, Clive E. Clinical Pharmacy and Therapeutics London. 3rd ed. London, United Kingdom: Churchill Livingstone; 2003. p. 791-3.
Snekhalatha U, Anburajan M, Venkatraman B, Menaka M. Evaluation of complete Freund’s adjuvant-induced arthritis in a Wistar rat model. Z Rheumatol 2013;72:375-82.
Greene RJ, Harris ND. Pathology and Therapeutics for Pharmacists: A Basis for Clinical Pharmacy Practice. 3rd ed. London: Pharmaceutical Press; 2008.
Mahajan A, Tandon VR. Antioxidants and rheumatoid arthritis. J Indian Rheumatol Assoc 2004;12:4:139-42.
Roy S, Sannigrahi S, Ghosh B, Pusp P, Roy T. Combination therapy of dexamethasone with epigallocatechin enhances tibiotarsal bone articulation and modulates oxidative status correlates with cartilage cytokines expression in the early phase of experimental arthritis. Eur J Pharmacol 2013;698:444-54.
Dipiro JT, Talbert RL, Yee GC, Matzke GR, Wells BG, Posey LM. Pharmacotherapy: A Pathophysiologic Approach. 7th ed. New York: McGraw-Hill Medical; 2014.
Hansen SM. Rheumatoid arthritis and work. Faculty of Health and Medical Science, University of Copenhagen, Graduate School at the Faculty of Health and Medical Sciences. Copenhagen: University of Copenhagen; 2016.
Hendawy OM, Ahmed WM, Abosaif AA, Mahmoud FA. Effect of atorvastatin and Vitamin D on Freund’s adjuvant-induced rheumatoid arthritis in rat. J Bioequiv Availab 2015;7:090-4.
Bendele A. Animal models of rheumatoid arthritis. J Musculoskelet Neuronal Interact 2001;1:377-85.
Wilsher M. Erdosteine: A viewpoint. Drugs 1996;52:882.
Dal Negro RW. Erdosteine: Antitussive and anti-inflammatory effects. Lung 2008;186:70-3.
Şener G, Aksoy H, Şehirli O, Yüksel M, Aral C, Gedik N, et al. Erdosteine prevents colonic inflammation through its antioxidant and free radical scavenging activities. Dig Dis Sci 2007;52:2122-32.
Hoza J, Salzman R, Starek I, Schalek P, Kellnerova R. Efficacy and safety of erdosteine in the treatment of chronic rhinosinusitis with nasal polyposis-a pilot study. Rhinology 2013;51:323-7.
Yagmurca M, Fadillioglu E, Erdogan H, Ucar M, Sogut S, Irmak MK. Erdosteine prevents doxorubicin-induced cardiotoxicity in rats. Pharmacol Res 2003;48:377-82.
Moretti M, Marchioni CF. An overview of erdosteine antioxidant activity in experimental research. Pharmacol Res 2007;55:249-54.
Kala C, Ali SS, Abid M, Sharma US, Khan NA. Evaluation of in-vivo antiarthritic potential of methanolic extract of Cheilocostus speciosus rhizome. J Appl Pharm Sci 2015;5:46-53.
Dasgupta S, Ghosh SK, Ray S, Mazumder B. Solid lipid nanoparticles (SLNs) gels for topical delivery of aceclofenac in vitro and in vivo evaluation. Curr Drug Deliv 2013;10:656-66.
Dasgupta S, Ghosh SK, Ray S, Kaurav SS, Mazumder B. In vitro in vivo studies on lornoxicam loaded nanoemulsion gels for topical application. Curr Drug Deliv 2014;11:132-8.
Hasan UH, Uttra AM, Rasool S. Evaluation of in vitro and in vivo anti-arthritic potential of Berberis calliobotrys. Bangladesh J Pharmacol 2015;10:807-19.
Rohmah RN, Widjajanto E, Fatchiyah F. Protective effect of CSN1S2 protein of goat milk on ileum microstructure and inflammation in rat- CFA-induced rheumatoid arthritis. Asian Pac J Trop Dis 2015;5:564-8.
Vandever LA. How are Rheumatoid Arthritis and Anaemia Connected, Healthline Newsletter; 2018. Available from: https://www.healthline. com/health/rheumatoid-arthritis-and-anemia. [Last accessed on 2021 Sep 26].
Patil KS, Suryavanshi J. Effect of Celastrus paniculatus Willd. Seed on adjuvant induced arthritis in rats. Pharmacogn Mag 2007;3:177.
Published
How to Cite
Issue
Section
Copyright (c) 2021 BANYLLA SYNMON, SANHATIDUTTA ROY, SUTAPA BISWAS MAJEE, MEGHNA PAUL, SANDIPAN DASGUPTA
This work is licensed under a Creative Commons Attribution 4.0 International License.
The publication is licensed under CC By and is open access. Copyright is with author and allowed to retain publishing rights without restrictions.