ANTI-ULCER ACTIVITY OF HYDROALCOHOLIC EXTRACT OF PIPER BETLE LEAF ON EXPERIMENTAL ANIMALS

Authors

  • URMISTHA SARKAR Department of Pharmacology, Netaji Subhas Chandra Bose Institute of Pharmacy, Chakdaha, Nadia, India.
  • ANKIT SAHA Department of Pharmacology, Netaji Subhas Chandra Bose Institute of Pharmacy, Chakdaha, Nadia, India.
  • MRITYUNJOY MAJUMDAR Department of Pharmacology, Netaji Subhas Chandra Bose Institute of Pharmacy, Chakdaha, Nadia, India.

DOI:

https://doi.org/10.22159/ajpcr.2019.v12i7.33232

Keywords:

Antiulcer,, Piper betle,, Pyloric ligation,, Stress-induced model

Abstract

Objective: The main objective of this study is to establish the anti-ulcer activity of hydroalcoholic extract of Piper betle leaf on experimental animals based on previously existing aspects such as antioxidant, antihistaminic, and antimicrobial properties of P. betle leaf.

Methods: The leaves were collected, shed dried, and extracted by the Soxhlet apparatus using 70% ethanol. The anti-ulcer activity of the extract was evaluated in albino Wistar rats employing pyloric ligation and stress-induced antiulcer models. Ranitidine was served as a standard drug in both the models. The significance of activity was assessed using a one-way analysis of variance followed by Dunnett’s post-parametric test.

Results: In the pyloric ligation model, the untreated control has shown 4.3 mEq/l of acidity, whereas the ranitidine-treated standard group shown 2 mEq/l and P. betle has shown 2.5 mEq/l acidity, respectively. In the stress-induced antiulcer model, the activity was more prominent, in the untreated control, there was 26 number of sores present, whereas the standard group showed only one number of ulcer sore, and in the P. betle treated group, there was four number of ulcer sores present.

Conclusion: In the present study, P. betle exhibited potent antiulcer potential while compared with the untreated control and the activity is comparable with standard ranitidine. From the above findings, it can correlate the use of betel leaf as a digesting or gastroprotective agent.

Downloads

Download data is not yet available.

References

Chauhan I, Sharma A, Gangwar M, Gautam MK, Singh A, Goel RK. Gastric antiulcer and ulcer healing effects of Punica granatum L. Peel extract in rats: Role of offensive and defensive mucosal factors and oxidative stress. Int J Pharm Pharm Sci 2017;9:6-11.

Venkateswarlu K, Vijayabhaskar K, Krishna OS, Devanna N, Sekhar KC. Evaluation of anti-ulcer activity of hydro alcoholic extracts of Abutilon indicum, Helianthus annuus and combination of both against ethanol and pyloric ligation induced gastric ulcer in albino Wistar rats. Br J Pharm Res 2015;5:42.

Lanas A, Chan FK. Peptic ulcer disease. Lancet 2017;390:613-24.

Martin DF, Montgomery E, Dobek AS, Patrissi GA, Peura DA. Campylobacter pylori, NSAIDS, and smoking: Risk factors for peptic ulcer disease. Am J Gastroenterol 1989;84:1268-72.

Weil J, Colin-Jones D, Langman M, Lawson D, Logan R, Murphy M, et al. Prophylactic aspirin and risk of peptic ulcer bleeding. BMJ 1995;310:827-30.

Wakefield AJ, Sawyerr AM, Dhillon AP, Pittilo RM, Rowles PM, Lewis AA, et al. Pathogenesis of crohn’s disease: Multifocal gastrointestinal infarction. Lancet 1989;2:1057-62.

Sharifi-Rad M, Fokou PVT, Sharopov F, Martorell M, Ademiluyi AO, Rajkovic J, et al. Antiulcer agents: From plant extracts to phytochemicals in healing promotion. Molecules 2018;23:E1751.

Tripathi KD. Essentials of Medical Pharmacology. 8th ed. London: Jaypee Brothers Medical Publishers; 2019.

Usser M. Causes of peptic ulcer. A selective epidemiologic review. J Chronic Dis 1967;20:435-56.

Harini SS, Sougandhi PR, Tenkayala DS, Gopinath KR. Antioxidant activity (phenol and flavonoid content) of three different cultivars of Piper betle leaf. (Piperaceae). J Drug Deliv Ther 2018;8 Suppl 5:143-8.

Rekha VP, Kollipara M, Gupta BR, Bharath Y, Pulicherla KK. A review on Piper betle L.: Nature’s promising medicinal reservoir. A J Ethol 2014;1:276-89.

Hajare R, Darvhekar VM, Shewale A, Patil V. Evaluation of antihistaminic activity of Piper betle leaf in guinea pig. Afr J Pharm Pharmacol 2011;5:113-7.

Datta A, Ghoshdastidar S, Singh M. Antimicrobial property of Piper betle leaf against clinical isolates of bacteria. Int J Pharm Sci Res 2011;2:104-9.

Hung CR, Wang PS. Gastric oxidative stress and hemorrhagic ulcer in Salmonella typhimurium infected rats. Eur J Pharmacol 2004;491:61-8.

Walum E. Acute oral toxicity. Environ Health Perspect 1998;106 Suppl 2:497-503.

Kokate CK, Purohit AP, Gokhale SB. Pharmacognosy. 30th ed. Pune, India: Nirali Prakashan; 2005.

Kulkarni SK. Hand Book of Experimental Pharmacology. 4th ed. New Delhi: Vallabh Prakashan; 2012.

Jadhav SA, Prasanna SM. Evaluation of antiulcer activity of Ziziphus oenoplia (L) Mill. Root in rats. Asian J Pharm Clin Res 2011;1:92-5.

Deshpande SS, Shah GB, Parmar NS. Antiulcer activity of Tephrosia purpurea in rats. Indian J Pharmacol 2003;35:168-72.

Sayed DA, Fahmy SR, Soliman AM, Hussein NS. Antiulcerogenic efficacy of ethanolic extract of Vitis vinifera leaves in rats. Int J Pharm Pharm Sci 2016;8:163-72.

Kitagawa H, Fujiwara M, Osumi Y. Effects of water-immersion stress on gastric secretion and mucosal blood flow in rats. Gastroenterology 1979;77:298-302.

Malairajan P, Gopalakrishnan G, Narasimhan S, Veni KJ. Evalution of anti-ulcer activity of Polyalthia longifolia (Sonn.) thwaites in experimental animals. Indian J Pharmacol 2008;40:126-8.

Gill NS, Garg M, Bansal R, Sood S, Muthuraman A, Bali M, et al. Evaluation of antioxidant and antiulcer potential of Cucumis sativum L. seed extract in rats. Asian J Clin Nutr 2009;1:131-8.

Majumdar M, Samanta A, Roy A. Study of wound healing activity of different formulations of Nigella sativa seed extract. Res J Pharm Technol 2016;9:2097-105.

Published

07-07-2019

How to Cite

URMISTHA SARKAR, ANKIT SAHA, and MRITYUNJOY MAJUMDAR. “ANTI-ULCER ACTIVITY OF HYDROALCOHOLIC EXTRACT OF PIPER BETLE LEAF ON EXPERIMENTAL ANIMALS”. Asian Journal of Pharmaceutical and Clinical Research, vol. 12, no. 7, July 2019, pp. 226-9, doi:10.22159/ajpcr.2019.v12i7.33232.

Issue

Section

Original Article(s)