Analgesic Activity of Ethanol Leaf Extract of Saccharum officinarum

doi.org/10.26538/tjnpr/v5i6.27

Authors

  • Jude E. Okokon Department of Pharmacology and Toxicology, Faculty of Pharmacy, University of Uyo, Uyo, Nigeria
  • John A. Udobang Department of Clinical Pharmacology and Therapeutics, Faculty of Basic Clinical Sciences, University of Uyo, Uyo, Nigeria
  • Koofreh Davies Department of Physiology, Faculty of Basic Medical Sciences, University of Uyo, Uyo, Nigeria
  • Utibe A. Edem Department of Pharmacology and Toxicology, Faculty of Pharmacy, University of Uyo, Uyo, Nigeria
  • Augustine I. Bassey Department of Clinical Pharmacology and Therapeutics, Faculty of Basic Clinical Sciences, University of Uyo, Uyo, Nigeria

Keywords:

Saccharum officinarum, Analgesic, Pain, Ethanol extract, Ethnomedicine

Abstract

Pain is one of the commonest symptoms reported to physicians and health workers and causes more frequent visits to health facilities than most other symptoms. Diverse methods and substances including plant parts are being used to  treat pain. Saccharum officinarum (sugar cane) which is used in traditional medicine to treat arthritis was therefore  investigated to authenticate its ability to ameliorate pain. The ethanol leaf extract of S. officinarum (170, 340, 510 mg/kg) was evaluated for analgesic activity against experimentally-induced pain in mice using three standard models of acetic acid-induced writhing, formalin-induced hind paw licking and thermally-induced pain. The median lethal dose (LD50) of the extract using Lorke’s method, was estimated to be 173 g/kg. The leaf extract significantly (p<0.005-0.001) inhibited pain in all the models tested in a dose-dependent fashion. Acetic acid-induced model is used to test for pain of visceral origin. Formalin causes biphasic pain, first phase being neurogenic, while the second phase is peripheral and central. Hot plate model is used to test for pain of central origin. Acetylsalicylic acid (ASA) induces analgesia through activation of opiod receptors and can be used to test for pain of peripheral and central origin. Therefore, the apparent similarity between the results of the extract and ASA indicates that they might work in the same manner to reduce pain sensation. The findings of this study show that the leaf extract possesses analgesic activity which confirms its use in traditional medicine in the treatment of pain. 

References

Hartwell JL. Plants used against cancer. A survey. Lloydia. 1971; 34(1):30-34.

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

Ojewunmi O, Oshodi T, Ogundele O, Micah C, 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. Int J Biochem Res Rev. 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. Mol. 2014;19:13147-13160.

Palaksha MN, Ravishankar K, GirijaSastry V. Biological evaluation of in vivo diuretic, and antiurolithiatic activities of ethanolic leaf extract of Saccharum officinarum. IndoAm 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.

Lorke D. A new approach to practical acute toxicity testing. Arch Toxicol.1983; 54:275-286.

Santos AR, Cechinel Filho V, Niero R, Viana AM, Moreno FN, Campos MM, Yunes RA, Calixto JB. Analgesic effects of callus culture from selected species of Phyllanthus. J Pharm Pharmacol. 1994; 46:755-759.

Nwafor PA, Nwajiobi N, Uko IE, Obot JS. Analgesic and anti-inflammatory activities of an ethanol extract of Smilax krausiana leaf in mice. Afr J Biomed Res. 2010; 13:141-148.

Hunskaar S, Hole K. The formalin test in mice. Dissociation between inflammatory pain. Pain. 1987; 30:103-114.

Okokon JE, Nwafor PA. Antiinflammatory, analgesic and antipyretic activities of ethanolic root extract of Croton zambesicus. Pak J Pharm Sci. 2010; 23:383-390.

Vaz ZR, Cechinel V, Yunes RA, Calixto JB.Antinociceptive action of 2-(4-bromobenzoyl)-3-methyl-4- 6-dimethoxy bezofuran, a novel xanthoxyline derivative of; chemical and thermal models of nociception in mice. J Pharm Exp Ther. 1996; 278:304-312.

Tukey JW. Comparing Individual Means in the Analysis of Variance. Int Biomet Soc. 1949; 5(2):99-114.Amico-Roxas M, Caruso A, Trombadore S, Scifo R, Scapagnime U. Gangliosides antinociceptive effects in rodents. Arch Int Pharmacodyn Ther. 1984; 272:103-117.

Nwafor PA, Jacks TW, Ekanem AU. Analgesic and antiinflammatory effects of methanolic extract of Pausinystalia mecroceras stem bark in rodents. J Pharmacol. 2007; 3:86-90.

Deraedt R, Jougney S, Falhout M. Release of Prostaglandin E and F in an algogenic reaction and its inhibition. Eur J Pharm. 1980; 51:17-24.

Bentley GA, Newton SH, Starr J. Studies on the antinociceptive action of agonist drugs and their interaction with opioid mechanisms. Br J Pharm. 1983; 79:125-134.

Franzotti EM, Santos CVF, Rodrigues HMSL, Mourao RHV, Andrade MR, Antoniolli AR. Anti-inflammatory, analgesic activity and acute toxicity of Sida cordifolia L. JEthnopharmacol. 2002; 72:273-278.

Vaz ZR, Risley EA, Calixto JB. Analgesic effect of the herbal medicine catuama in thermal and chemical models of nociception in mice. Phytother Res. 1997; 11:101-106.

Wibool R, Sae WC, Reanmongkol W, Wongnawaa M. Antinociceptive activity of the methanolic extract of Kaempferia galangal Linn. in experimental animals. JEthnopharmacol. 2008. 118: 225-230.

Lu YY, AO ZH, LU ZM, XU XT, Zhang XM, Dou WF, Xu ZH. Analgesic and anti-inflammatory effects of the dry matter of culture broth of Termitomyces albuminosus and its extracts. J Ethnopharmacol. 2008; 120(30:432-436: 10.1016/j.jep.2008.09.021.Epub2008sep27.PMID:18948177

Berken T, Ostunes L, Lermioglu F, Ozer A. Antiinflammatory analgesic and antipyretic effect of an aqueous extract of Erythraea ceulaurum. Planta Med. 1981;57:34-37.

Turner RA. Screening methods in Pharmacology. Vol 1. Academic Press. New York; 1995. 85-106 p.

Liang YC, Huang YT, Tsau SH, Lin-Shiau SY, Chen CF, Lin JK. Suppression of inducible cyclo-oxygenase and inducible nitric acid synthase by apigenia and relatedflavonoid in mouse macrophages. Carcinogen. 1999;20:1945-1952.

Carlo Di G, Mascolo N, Izzo AA, Capasso F. Flavonoids, old and new aspects of a class of natural therapeutic drugs. Life Sci. 1999; 65:337-353.

Middleton E Jr; Kandaswami C, Theoharides TC. The effects of plant flavonoids on mammalian cells: Implications for inflammation, heart disease, and cancer. Pharmacol Rev. 2000. 52:673-751.

Suh HW, Song DK, Son KH, Wie MB, Lee KH, Jung KY, Do JC, Kim YH. Antinociceptive mechanisms of Dipsacus saponin C administered intracerebroventricu-larly in the mouse. Gen Pharmacol. 1996. 27:1167-1172.

Rajendran NN, Thirugnanasambandam P, Viswanathan S, Parvathavarthini S, Ramaswamy S. Antinociceptive pattern of flavone and its mechanism as tested by formalin assay. Indian J Exp Biol. 2000; 38:182-185.

Otuki MF, Ferreira J, Lima FV, Meyre-Silva C, Malheiros Â, Muller LA, Cani GS, Santos ARS, Yunes RA, Calixto JB. Antinociceptive properties of mixture of α-amyrin and β-amyrin triterpenes: Evidence for participation of protein kinase C and protein kinase A pathways. J Pharmacol ExpTher. 2005. 313:310-318.

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Published

2021-06-01

How to Cite

Okokon, J. E., Udobang, J. A., Davies, K., Edem, U. A., & Bassey, A. I. (2021). Analgesic Activity of Ethanol Leaf Extract of Saccharum officinarum: doi.org/10.26538/tjnpr/v5i6.27. Tropical Journal of Natural Product Research (TJNPR), 5(6), 1142–1145. Retrieved from https://tjnpr.org/index.php/home/article/view/639