Antiulcerogenic activity of leaf extract of Saccharum officinarum (Poaceae) in rodents

Main Article Content

Utibe A. Edem
John A. Udobang
Augustine L. Bassey
Uchechukwu L. Iyanyi
Jude E. Okokon

Abstract

Background:Saccharum officinarum (Family-Poaceae) is used in Ibibio ethnomedicine for the treatment of various diseases such as malaria and gastrointestinal disorders. The study aimed to evaluate the antiulcerogenic activity of the leaf extract against experimentally-induced ulcer in rats.


 


 Methods:The leaf extract  of S. officinarum (170-510 mg/kg) was investigated for antiulcer activity in rodents using indomethacin, ethanol and histamine-induced ulcer  models in overnight fasted Wistar rats weighing 125-150 g. The rats were randomized into different groups and treated with extract and ulcerogens. The stomachs of the animals were removed, examined for ulcerations and scored accordingly.


   


Results: The leaf extract (170-510 mg/kg) was found to exert significant (p<0.05-0.001) and dose-dependent activity against indomethacin, ethanol and histamine-induced ulcers.


 


Conclusion: These results suggest that the leaf extract of Saccharum officinarum possesses antiulcerogenic potential which is due to the activities of the phytochemical constituents which can be explored for the treatment of ulcers.

Downloads

Download data is not yet available.

Article Details

How to Cite
A. Edem, U., A. Udobang, J., L. Bassey, A., L. Iyanyi , U., & E. Okokon, J. (2023). Antiulcerogenic activity of leaf extract of Saccharum officinarum (Poaceae) in rodents. Nigerian Journal of Pharmaceutical and Applied Science Research, 12(2), 22–27. https://doi.org/10.60787/nijophasr-v12-i2-509
Section
Articles

References

. Hartwell, J.L. Plants used against cancer. A survey. Lloydia 1967-1971; 30–34.

. Palaksha MN, Ravishankar K and Girijasastry V. Phytochemical screening and evaluation of in-vitro antibacterial and anthelmintic activities of Saccharum officinarum leaf extracts. World J Pharmacy and Pharmaceutical Sci, 2013; 2(6):5761-5768.

.Ojewunmi O, Oshodi T, Ogundele O, Micah C and Adenekan S. Evaluation of the anti-diabetic and antioxidant activities of aqueous extracts of Morinda lucida and Saccharum officinarum leaves in alloxan-induced diabetic rats. Intl J. Biochemistry Res Review, 2013; 3(3): 266-277.

.Sun J, He X, Zhao M, Li L, Li C, Dong Y. Antioxidant and Nitrite-Scavenging capacities of phenolic compounds from sugarcane (Saccharum officinarum L.) Tops Molecules 2014; 19: 13147-13160.

. Palaksha, M. N., Ravishankar, K., GirijaSastry, V. Biological evaluation of in vivo diuretic, and antiurolithiatic activities of ethanolic leaf extract of Saccharum officinarum. Indo Amer J Pharm Res. 2015; 5(06): 2232-2238.

.Okokon JE, Udoh AE, Nyong EE, Eno L, Udo NM. Psychopharmacological studies on leaf extract of Saccharum officinarum. Trop J Nat Prod Res. 2019; 3(2):26-30.

. Okokon JE, Davies K, Edem UA, Bassey AL, Udobang JA. Analgesic activity of ethanol leaf extract of Saccharum officinarum. Trop J Nat Prod Res. 2021; 5(6):1142-1145.

. Okokon JE, Mobley R, Edem UA, Bassey AL, Fadayomi I, Horrocks P, Drijfhout F, Li WW. In vitro and in vivo antimalarial activities and chemical profiling of sugarcane leaves. Science Reports 2022; 41598 Article No:14391 doi. org/ 10. 1038/ s41598 -022-14391-8.

.Edem UA, Okokon JE, Bassey AL, Okokon PJ. Antioxidative stress and hepatoprotective activities of leaf extract and fractions of Sacharum officinarum in Plasmodium berghei infected mice. J Current Biomed Res. 2022;2(4):317-337.

.Edem UA, Udobang JA, Okokon JA. Antiinflammatory and antipyretic activities of ethanol leaf extract of Saccharum officinarum in mice. Eur. J Pharm Med Res 2023;10(8):29-36.

.Obidike IC, Amodu B, Emeje MO. Antimalarial properties of SAABMAL®: an ethnomedicinal polyherbal formulation for the treatment of uncomplicated malaria infection in the tropics. Indian J Med Res. 2015; 141(2): 221–227.

.Akwetey GA, Achel DG. Ethnopharmacological use of herbal remedies for the treatment of malaria in the Dangme West District of Ghana. J Ethnopharmacol 2010; 129 (3): 367-376.

.Singh A, Lal UR,Mukhtar HM, Singh PS, Shah G, Dhawan RK. Phytochemical profile of sugarcane and its potential health aspects. Pharmacogn Rev. 2015; 9(17): 45–54.

.Coutinho ID,Baker JM, Ward JL, Beale MH, Creste S,Cavalheiro AJ. Metabolite profiling of sugarcane genotypes and identification of flavonoid glycosides and phenolic acids. J. Agric. Food Chem.2016,:64(21): 4198–4206.

. Alphin RS, Ward JW. Action of hexopyrronium bromide on gastric secretion in dogs and on gastric secretion and ulceration in rats. Archives Internationales de Pharmacodynamie et de Therapie 1967;270: 128 -140.

. Nwafor PA, Effraim KD, Jacks TW. Gastroprotective effects of aqueous extracts of Khaya senegalensis bark on indomethacin – induced ulceration in rats. West Afr. J. Pharmacol and Drug Res 1996;12:46 – 50.

.Zaidi, S. H., Mukerji, B. Experimental peptic ulceration. Part 1. The significance of mucus barrier. Ind J Med Res. 1958; 46:27 – 37.

. Nwafor PA, Okwuasaba FK, Binda lG. Antidiarrhoeal and antiulcerogenic effects of methanolic extracts of Asparagus pubescens root in rats. J Ethnopharmacol 2000;72:421 – 427.

. Maity, S.,Vedasiromoni, J. R.,Ganguly, D. K. Antiulcer effect of the hot water extract of black tea (Camellia sinensis). J. Ethnopharmacol. 1995;46: 167 – 174.

. Rainsford KD. The effects of 5- lipoxygenase inhibitors and leukotriene antagonists on the development of gastric lesions induced by nonsteroidal anti-inflammatory drugs in mice. Agents and Action 1987; 21:316 – 319.

. Bhargava KP, Gupta MB, Tangri KK. Mechanism of ulcerogenic activity of indomethacin and oxyphenbutazone. Eur. J.Pharmacol. 1973; 22:191 – 195.

.Hayllar J, Bjarnason I. NSAIDS, COX-2 inhibitor and the gut. Lancet 1995;346 - 522.

. Hiruma-Lima CA, Calvo TR, Rodriguez CM, Andrade F D P, Vilegas W, Brito ARM. Antiulcerogenic activity of Alchornea castaneaefolia effects on somatostatin, gastrin and prostaglandin. J. Ethnopharmacol. 2006;104: 215 – 224.

. Salim, A. S. Removing oxygen derived free radicals stimulates healing of ethanol- induced erosive gastritis in the rats. Digestion 1990;47: 24 – 28.

. Pihan G, Regillo C, Szabo S. Free radicals and lipid peroxidation in ethanol or aspirin – induced gastric mucosa injury. Digestive Diseases and Sciences 1987; 32: 1395 – 1401.

. Whittle BJR, Oren-Wolman, N, Guth PH. Gastric vasoconstrictor actions of leukotriene C4 and PGF2? and thromboxane mimetic (U-4669) on rats submucosal microcirculation in vivo. Am J Physiol 1985; 248: G580 – G586.

. Cho CH, Pfeiffer CJ. Gastrointestinal ulceration in the guinea pigs in response to dimaprit, histamine and H1 and H2 blocking agents. Digestive Disease Sci. 1981; 26:306 – 311.

. Di Carlo G, Mascolo N, Izzo AA, Capasso, F. Flavonoids: old and new aspects of a class of a natural therapeutic drug. Life sci 1999; 64: 337 – 353.

. Zayachkivska OS, Konturek SJ, Drozdowicz D, Konturek PC, Brzozowski, T, Ghegotsky MR. Gastroprotective effects of flavonoids in plants extracts. J. Physiol. Pharmacol. 2005; 56: 216 - 231.

. Borrelli F, Izzo AA. The plant kingdom as source of anti ulcer remedies. Phytother Res. 2000;14: 581 – 591.

. Agwu CN, Okunji CO. Gastrointestinal studies of Pyrenacantha staudtii leaf extracts. J. Ethnopharmacol. 1986;15: 45 – 55.

. Lewis, D.A., Hanson, D. Anti-ulcer drugs of plants origin. Progr. Med. Chem. 1991; 28:208 – 210.

. Kohno Y, Egawa Y, Itoh S, Nagaoka S, Takahashi M, Mukai K. Kinetic study of quenching reaction of singlet oxygen and scavenging reaction of free radical by squalene in n-butanol. Biochim Biophys Acta. 1995;1256:52–56.

.Ponnamma SU, Manjunath K. (2012). GC-MS analysis of phytocomponents in the methanolic extract of Justicia wyaadensis (NEES) T. Anders. Int J Pharma Bio Sci 2012;3:570-576.

. Khan SL, Siddiqui FA. Beta-Sitosterol: As Immunostimulant, Antioxidant and Inhibitor of SARS-CoV-2 Spike Glycoprotein. Arch Pharmacol Ther. 2020; 2(1):12-16.