Pharmacological evaluation of the ethanolic extract of alpinia calcarata rhizomes for anti-asthmatic activity
DOI:
https://doi.org/10.37022/jpmhs.v8i4.152Keywords:
Alpinia calcarata, Anti-asthmatic activity, Histamine-induced bronchoconstriction, Milk-induced eosinophilia, Flavonoids, Phytochemical screening, AntioxidantAbstract
The present study investigates the anti-asthmatic activity of the ethanolic extract of Alpinia calcarata rhizomes (EEAC) using histamine aerosol-induced bronchoconstriction in guinea pigs and milk-induced leukocytosis and eosinophilia in mice. The rhizomes were collected, authenticated, shade-dried, powdered, and extracted using ethanol through Soxhlet extraction, yielding 17% w/w extract. Preliminary phytochemical screening revealed the presence of flavonoids, tannins, phenols, steroids, proteins, carbohydrates, and cardiac glycosides. Acute toxicity studies, conducted as per OECD guidelines 423, showed no mortality up to 2000 mg/kg, indicating the extract’s safety. In vivo studies demonstrated significant protection against histamine-induced bronchospasm, with maximum protection (62.62%) observed at 200 mg/kg, comparable to the standard drug chlorpheniramine maleate. The extract also significantly reduced milk-induced leukocytosis and eosinophilia, indicating anti-inflammatory potential. The anti-asthmatic effects may be attributed to the presence of flavonoids and steroids, known for their bronchodilatory and antioxidant properties. The results validate the traditional use of Alpinia calcarata in asthma management and suggest further studies to isolate and characterize the bioactive compounds responsible for these effects.
Downloads
References
Abramson MJ, Perret JL, Dharmage SC. Distinguishing adult-onset asthma from COPD: a review and a new approach. Int J Chron Obstruct Pulmon Dis. 2014;9:945-962.
Rutkowski K, Sowa P, Rutkowska-Talipska J. Allergic diseases: the price of civilisational progress. Postepy Dermatol Alergol. 2014;31(2):77-83.
Tripathi KD. Essentials of Pharmacology. 6th ed. New Delhi: Jaypee Brothers Medical Publishers; 2008.
Mohan H. Textbook of Pathology. 6th ed. New Delhi: Jaypee Brothers Medical Publishers; 2010.
Craig CR, Stitzel RE. Modern Pharmacology with Clinical Applications. 5th ed. Philadelphia: Lippincott Williams & Wilkins; 2003.
Cookson WO, Moffatt MF. Genetics of asthma and allergic disease. Hum Mol Genet. 2000;9:2359-2364.
Barnes KC. Evidence for common genetic elements in allergic disease. J Allergy Clin Immunol. 2000;106:192-200.
Dunnill MS. The pathology of asthma, with special reference to the changes in the bronchial mucosa. J Clin Pathol. 1960;13:27-33.
Akers IA, Parsons M, Hill MR. Mast cell tryptase stimulates human lung fibroblast proliferation via protease-activated receptor-2. Am J Physiol Lung Cell Mol Physiol. 2000;278:L193-L201.
Williams CM, Galli SJ. The diverse potential effector and immunoregulatory roles of mast cells in allergic disease. J Allergy Clin Immunol. 2000;105:847-859.
Fahy JV. Reducing IgE levels as a strategy for the treatment of asthma. Clin Exp Allergy. 2000;30(Suppl 1):16-21.
Barnes PJ. Anti-IgE therapy in asthma: rationale and therapeutic potential. Int Arch Allergy Immunol. 2000;123:106-204.
Milgrom H, Fick RB Jr, Su JQ, et al. Treatment of allergic asthma with monoclonal anti-IgE antibody. N Engl J Med. 1999;341:1966-1973.
Zieg G, Lack G, Harbeck RJ, Gelfand EW, Leung DY. In vivo effects of glucocorticoids on IgE production. J Allergy Clin Immunol. 1994;94:222-230.
Edmonds ML, Camargo CA Jr, Brenner BE, Rowe BH. Replacement of oral corticosteroids with inhaled corticosteroids in the treatment of acute asthma following emergency department discharge: a meta-analysis. Chest. 2002;121:1798-1805.
Rainsford KD. History and development of the salicylates. In: Rainsford KD, editor. Aspirin and Related Drugs. London: Taylor & Francis; 2004. p. 1-23.
Phillips T, Leeuwenburgh C. Lifelong aspirin supplementation as a means to extending lifespan. Rejuvenation Res. 2004;7(4):243-251.
Pellegatta F, Bertelli AA, Staels B, Duhem C, Fulgenzi A, Ferrero ME. Different short- and long-term effects of resveratrol on nuclear factor-kappaB phosphorylation and nuclear appearance in human endothelial cells. Am J Clin Nutr. 2003;77:1220-1228.
Paulus HE. Clinical trial design for evaluating combination therapies. Br J Rheumatol. 1995;34(Suppl 2):92-95.
Parkinson JF. Lipoxin and synthetic lipoxin analogs: an overview of anti-inflammatory functions and new concepts in immunomodulation. Inflamm Allergy Drug Targets. 2006;5:91-106.
Sapa S, Bubici C, Zazzeroni F, Pham CG, Kuntzen C, Knabb JR, et al. New approaches to the treatment of inflammatory disorders: small molecule inhibitors of p38 MAP kinase. Curr Top Med Chem. 2006;6:113-149.
Paik JH, Ju JH, Lee JY, Boudreau MD, Hwang DH. Two opposing effects of non-steroidal anti-inflammatory drugs on the expression of the inducible cyclooxygenase. J Biol Chem. 2000;275:28173-28179.
Otterness IG. The discovery of drugs to treat arthritis: a historical view. In: Merluzzi VI, Birkhiuser J, Adams J, editors. The Search for Anti-inflammatory Drugs. Basel: Birkhäuser; 1995. p. 1-26.
Nathoo N, Barnett GH, Golubic M. The eicosanoid cascade: possible role in gliomas and meningiomas. J Clin Pathol. 2004;57:6-13
Published
How to Cite
Issue
Section
Citations

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
Copyright © Author(s) retain the copyright of this article.


.