ANTI-INFLAMMATORY ACTIVITY OF MANILKARA ZAPOTA LEAF EXTRACT

Authors

  • Kamalakararao Konuku Department of Biochemistry, Aditya Degree and PG College, Kakinada, Andhra Pradesh, India
  • Krishna Chaithanya Karri Department of Chemistry, College of Natural and Computational Sciences Aksum University, Axum, Ethiopia
  • Velliyur Kanniappan Gopalakrishnan Department of Chemistry, College of Natural and Computational Sciences Aksum University, Axum, Ethiopia
  • Zenebe Hagos Department of Chemistry, College of Natural and Computational Sciences Aksum University, Axum, Ethiopia
  • Haftom Kebede Department of Biology, College of Natural and Computational Sciences Aksum University, Axum, Ethiopia
  • Tentu Kasi Naidu Department of Medical Laboratory Sciences, School of Health Sciences, Dilla University, Dilla, Ethiopia
  • Patricia Ponce Noyola Department of Life Sciences, University of Guanajuato, Mexico
  • John Dogulas Palleti Department of Life Sciences, University of Guanajuato, Mexico
  • Govinda Rao Duddukuri Rao Duddukuri Dept of Biochemistry and Molecular Biology, School of Biological Science, Central University of Kerala, India

DOI:

https://doi.org/10.22159/ijcpr.2017v9i4.20977

Keywords:

Manilkara zapota, COX-2, Phospholipase A2, Nil, Nil, IL-6, Nil

Abstract

Objective: Manilkara zapota is a medicinal plant which is native to Mexico and Central America, and widely distributed in India. Various parts of this plant are traditionally used for treatment of several diseases, including inflammation-associated ailments. The main aim of the present study is to evaluate the anti-inflammatory potential of ethyl acetate and methanolic extracts of M. zapota leaf.

Methods: In vitro secretary phospholipase A2 (PLA2) and 5-Lipoxygenase (5-LOX) assays and In vivo studies using carrageenan induced rat paw edema model were performed to assess the anti-inflammatory activity of M. zapota leaf extracts.

Results: In vitro studies suggest that M. zapota leaf extracts exhibited significant SPLA2 and 5-LOX inhibitory activities. In in vivo studies M. zapota leaf extracts showed dose dependent inhibition of carrageenan induced paw edema in rats. The anti-inflammatory activity of ethyl acetate leaf extract was superior to methanolic extract.

Conclusion: This study concluded that ethyl acetate leaf extract of M. zapotaexhibited significant anti-inflammatory activity and warranted further investigation to isolate and identify the components.

 

Downloads

Download data is not yet available.

References

Arai K, Lee F, Miyajima A, Miyatake S, Arai N, Yokota T. Cytokines: coordinators of immune and inflammatory responses. Annu Rev Biochem 1991;59:783-836.

Fadok VA, Voelker DR, Campbell PA, Cohen JJ, Bratton DL, Henson PM. Exposure of phosphatidylserine on the surface of apoptotic lymphocytes triggers specific recognition and removal by macrophages. J Immunol 1992;148:2207–16.

Hussain SP, Harris CC. Inflammation and cancer: an ancient link with novel potentials. Int J Cancer 2007;121:2373–80.

Bursinos LA, Karachalios T, Poultsides L, Malizos KN. Do steroids, conventional non-steroidal anti-inflammatory drugs and selective COX-2 inhibitors adversely affected fracture healing. J Musculoskeletal Neuronal Interact 2009;1:44-52.

Bjarnason I, Hayllar J, Macpherson AJ, Russell AS. Side effects of non-steroidal anti-inflammatory drugs on the small and large intestine in humans. Gastroenterology 1993;104:1832-47.

Mital Kaneria, Sumitra Chanda. Evaluation of antioxidant and antimicrobial properties of Manilkara zapota L. (chiku) leaves by sequential soxhlet extraction method. Asian Pacific J Trop Biomed 2012;3:S1526-S1533.

Madan Singh, Prashant Soni, Neeraj Upmanyu, Yogesh Shivhare. In vitro anti-arthritic activity of Manilkara zapota Linn. Asian J Pharm Technol 2011;1:123-4.

Reddanna P, Rao MK, Reddy C. Inhibition of 5-lipoxygenase by vitamin E. FEBS Lett 1985;193:39–43.

Sircar JC, Schwender CF, Johnson EA. Soybean lipoxygenase inhibition by non-steroidal anti-inflammatory drugs. Prosfaglandins 98325;1:393-6.

Winter CA, Risley EA, Nuss GW. Carrageenan-induced oedema in the hind paw of rat as an assay for anti-inflammatory activity. Proc Soc Exp Biol Ther 1962;111:544-7.

Warrier PK, Nambier VPK, Raman KC. Indian Medicinal Plants: A Compendium of 500 Species; 1994. p. 2, 180.

Hoareau L, Da Silva EJ. Medicinal plants, a re-emerging health aid. Electronic J Biotechnol 1999;2:56-70.

Jones WP, Chin YW, Kinghorn AD. The role of pharmacognosy in modernmedicine and pharmacy. Curr Drug Targets 2006;7:247-64.

Sosa S, Balicet MJ, Arvigo R, Esposito RG, Pizza C, Altinier GA. Screening of the topical anti-inflammatory activity of some central American plants. J Ethanopharmacol 2002;8:211–5.

Pascucci RA. Use of nonsteroidal anti-inflammatory drugs and cyclooxygenase-2 (COX-2) inhibitors: indications and complications. J Am Osteopath Assoc 2002;102:487–9.

Wolfe MM, David RL. Lichtenstein: gastrointestinal toxicity of non-steroidal anti-inflammatory drugs. N Engl J Med 1999;340:1888-99.

Hersberger M. Potential role of the lipoxygenase derived lipid mediators in atherosclerosis: leukotrienes, lipoxins and resolvins. Clin Chem Laboratory Med 2010;48:1063–73.

Cucurou C, BattioniJ P, Daniel R, Mansuy D. Peroxidase-like activity of lipoxygenase: different substrate specificity of potato 5-lipoxygenase and soybean 15-lipoxygenase and particular affinity of vitamin E derivatives for the 5-lipoxygenase. Biochim Biophys Acta 1991;1081:99–105.

Mansuy D, Cucurou C, Biatry B, Battioni JP. Soybean lipoxygenase-catalyzed oxidations by linoleic acid hydroperoxide: different reducing substrates and dehydrogenation of phenidone and BW755C. Biochem Biophysical Res Commun 1988;151:339–46.

Brooks RR, Carpenter JF, Jones SM, Ziegler TC, Pong SF. Carrageenan-induced acute paw inflammation model and its response to non-steroidal anti-inflammatory drugs. J Pharmacol Methods 1991;25:275–83.

Vinegar R, Schreiber W, Hugo R. Biphasic development of carrageenan edema on rats. J Pharmacol Exp Ther 1969; 66:96-10.

Ravi V, Saleem TSM, Patel SS, Raamamurthy J, Gauthaman K. Antiinflammatory effect of methanolic extract of Solanum nigrum Linn Berries. Int J Appl Res Nat Prod 2009;2:33-6.

Ahmadiani A, Hosseiny J, Semnanian S, Javan M, Saeedi F, Kamalinejad M, et al. Antinociceptive and anti-inflammatory effects of Eleagnus angustifolia fruit extract. J Ethnophamacol 2000;72:287–92.

Zainul AZ, Loo YW. Antinociceptive, anti-inflammatory and antipyretic properties of the aqueous extract of Bauhinia purpurea leaves in experimental animals. Med Princ Pract 2007;16:443-9.

Channa S, Dar A, Anjum S, Yaqoob M, Atta-Ur-Rahman. Anti-inflammatory activity of Bacopa monniera in rodents. J Ethnopharmacol 2006;104:286-9.

Crunkhorn P, Meacock SCR. Mediators of the inflammation induced in the rat paw by carrageenan. Br J Pharmacol 1971;42:392.

Boughton-Smith NK, Deckin AM, Follenfant RL, Whittle BJ, Garland LG. Role of oxygen radicals and arachidonic acid metabolites in the reverse passive arthus reaction and carrageenan paw oedema in the rat. Br J Pharmacol 1993;110:896-902.

Swingle KF, Shideman FE. Phases of the inflammatory response to subcutaneous implantation of a cotton pellet and their modification by certain anti-inflammatory agents. J Pharmacol Exp Ther 1972;185:226-34.

Mahat MA, Patil BM. Evaluation of anti-inflammatory activity of methanolic extracts of Phyllanthus amarus in experimental animal models. Indian J Pharma Sci 2007;4:33-5.

Desouky SK, Gamal-Eldeen AM. Cytotoxic and anti-inflammatory activities of some constituents from the floral buds of Syringa patula. Pharm Biol 2009;47:872-7.

Gupta M, Mazumder UK, Gomathi P. Thamil Selvan V. Anti-inflammatory evaluation of leaves of Plumeria acuminate. BMC Alternative Complementary Med 2006;6:36.

Kyei S, Koffuor GA, Boampong JN. The efficacy of aqueous and ethanolic leaf extracts of Pistia stratiotes Linn. in the management of arthritis and fever. J Med Biomed Sci 2012;1:29-37.

Muralidhar A, Sudhakar Babu K, Ravi Shankar T, Reddanna P, Reddy GV, Latha J. In vitro and in vivo anti inflammatory activity of Butea monosperma stem bark extract. Int J Pharm Thera 2010;1:44-51.

Oliver W. Inhibition of 5-Lipoxygenase product synthesis by natural compounds of plant origin. Planta Med 2007;73:1331-57.

Ding, XZ, Hennig R, Adrian TE. Lipoxygenase and cyclooxygenase metabolism: New insights in treatment and chemoprevention of pancreatic cancer. Mol Cancer 2003;2:10.

Balsinde J, Balboa MA, Insel PA, Dennis EA. Regulation and inhibition of phospholipase A2. Annu Rev Pharmacol Toxicol 1999;39:175-18.

Six DA, Dennis EA. The expanding superfamily of phospholipase A enzymes: classification and characterization. Biochim Biophys Acta 2000;1488:1-2:1-19

Da Silva SL, Calgarotto AK, Maso V, Damico DCS, Baldasso P, Veber CL, et al. Molecular modeling and inhibition of phospholipase A2 by polyhydroxy phenolic compounds. Eur J Med Chem 2009;44:312-21.

Lindahl M, Tagesson C. Selective inhibition of group II phospholipase A2 by quercetin. Inflammation 1993;17:573-82.

Chandra V, Jasti J, Kaur P, Betzel CH, Srinivasan A, Singh TP. First structural evidence of specific inhibition of phospholipases A2 by α-tocopherol (Vitamin E) and its implications in inflammation: crystal structure of the complex formed between phopholipase A2 and α-tocopherol at 1.8 Å resolution. J Mol Biol 2002;320:215-22.

Published

14-07-2017

How to Cite

Konuku, K., K. C. Karri, V. K. Gopalakrishnan, Z. Hagos, H. Kebede, T. K. Naidu, P. P. Noyola, J. D. Palleti, and G. R. D. Rao Duddukuri. “ANTI-INFLAMMATORY ACTIVITY OF MANILKARA ZAPOTA LEAF EXTRACT”. International Journal of Current Pharmaceutical Research, vol. 9, no. 4, July 2017, pp. 130-4, doi:10.22159/ijcpr.2017v9i4.20977.

Issue

Section

Original Article(s)