PHYTOCHEMICAL SCREENING AND IN-VIVO SCREENING OF ANTIULCER ACTIVITY ON FOENICULUM VULGARE SEEDS

Authors

  • Abhishek Singh
  • Deepak Basedia
  • B. K. Dubey

Abstract

Peptic ulcer disease and its complications remain the cause of significant morbidity worldwide, representing a major burden for health care resources. Although potent anti-ulcer drugs are available, most of them produce several toxicities, thus emphasizing the need to search for new alternatives. It is universally known as Fennel and is known by more than 100 names. It is a traditional and popular herb with a long history of use as a medicine. A series of studies showed that F. vulgare effectively controls numerous infectious disorders of bacterial, fungal, viral, mycobacterium, and protozoal origin. It has antioxidant, antitumor, chemopreventive, cytoprotective, hepatoprotective, hypoglycemic, and oestrogenic activities. Some of the publications stated that F. vulgare has a special kind of memoryenhancing effect and can reduce stress. The aim of present study was to evaluate antiulcer effect of F. vulgare. In the present study, different doses of the extract (100, 200, and 400 mg/kg) were evaluated for their effect on volume of gastric secretion, pH, total acidity, ulcer score, and ulcer index along with the standard drug ranitidine (50 mg/kg). In the single-dose study of the pylori ligation model, HEFV 100 mg/kg did not show any better activity when compared to the negative control. This indicates that the low dose of the extract is not an adequate dose to produce ulcer healing. This model showed that the highest dose of the plant extract (HEFV 400 mg/kg) has got better antisecretory activity as evidenced by reduction in the mean volume of gastric secretion, rise in pH, and reduction in total acidity (P<0.01) compared to the negative control. Significant reduction in ulcer index (measure of ulcerated area) was noted for HEFV 200 mg/kg (P<0.05) and HEFV 400 mg/kg (P<0.001) as compared to the negative control. Key words: Peptic ulcer, F. vulgare, antiulcer effect, Pylori ligation model

References

Susser M, Stein Z. Civilisation and peptic ulcer. Lancet 1962; 279: 116–19.

Sonnenberg A. Causes underlying the birth-cohort phenomenon of peptic ulcer: analysis of mortality data 1911–2000, England and Wales. Int J Epidemiol 2006; 35: 1090–97.

Warren JR, Marshall B. Unidentified curved bacilli on gastric epithelium in active chronic gastritis. Lancet 1983; 321: 1273–75.

Marshall BJ, Warren JR. Unidentified curved bacilli in the stomach of patients with gastritis and peptic ulceration. Lancet 1984; 323: 1311–15.

NIH Consensus Conference. Helicobacter pylori in peptic ulcer disease. NIH Consensus Development Panel on Helicobacter pylori in peptic ulcer disease. JAMA 1994; 272: 65–69.

Malfertheiner P, Megraud F, O’Morain C, et al. Current concepts in the management of Helicobacter pylori infection: the Maastricht III Consensus Report. Gut 2007; 56: 772–81.

Lancaster-Smith MJ, Jaderberg ME, Jackson DA. Ranitidine in the treatment of non-steroidal anti-inflammatory drug associated gastric and duodenal ulcers. Gut 1991; 32: 252–55.

Yeomans ND, Svedberg LE, Naesdal J. Is ranitidine therapy sufficient for healing peptic ulcers associated with non-steroidal anti-inflammatory drug use? Int J Clin Pract 2006; 60: 1401–07.

Mukherjee PK. Quality Control of Herbal Drugs, 2nd Edition, Business Horizons, 2007; 2-14.

Kokate CK. Ed. Practical Pharmacognosy, 4th Edn., Vallabh Prakashan: 1994; 112:120.

Arpana Gaur Mishra, Richa Singh, Neha Patil, Geeta Parkhe. Determination of total phenolic, flavonoid content, antioxidant and antimicrobial activity of gloriosa superba seed extract. Asian Journal of Pharmaceutical Education and Research. 2017; 6(2):12-17.

Organization for Economic Cooperation and Development. OECD Guidelines for the Testing of Chemicals. Acute Oral Toxicity -Up-And Down-Procedure. UDP; 425. France: OECD Publishing; 2000.

Dashputre NL, Naikwade NS. Evaluation of anti-ulcer activity of methanolic extract of Abutilon indicum Linn leaves in experimental rats. Int J Pharm Sci Drug Res. 2011; 3(2):97–100.

Melese E, Asres K, Asad M, Engidawork E. Evaluation of the antipeptic ulcer activity of the leaf extract of Plantago lanceolata L. in rodents. Phytother Res. 2011; 25(8):1174–1180.

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Published

2022-12-19

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Original Research Article