Antinociceptive and anti-arthritic properties of hydroethanolic leaf extract of Clausena anisata (Willd.) Hook. f. ex Benth (Rutaceae) in Rodents: possible mechanism of actions
Nyckelord:
Complete Freund's adjuvant, L-arginine-nitric oxide, nociception, antioxidant, rheumatoid arthritis, serotonergicAbstract
Summary: The leaves of Clausena anisata (Willd.) Hook. f. ex Benth (Rutaceae) is used in Traditional African medicine for the treatment of various ailments including arthritis. The present study sought to investigate the antinociceptive and anti-arthritic properties of hydroethanolic leaf extract of Clausena anisata (HeCA). HeCA (100, 200 or 400 mg/kg, p.o.) was administered 1 h before intraplantar injection of formalin 1%v/v in saline to evaluate antinociceptive effect. Moreover, its possible mechanism of antinociceptive action was investigated through pretreatment of mice with antagonists of receptors implicated in nociception. Anti¬inflammatory effect of the extract was investigated using the carrageenan-induced paw oedema and complete Freund's adjuvant (CFA)-induced arthritis models in rats. HeCA (400 mg/kg) treatment significantly reduced the duration of paw licking/biting during both in the early (42.12%) and late (75.79%) phases of formalin-induced nociception. However, the antinociceptive effect elicited by HeCA was reverse by pretreatment of mice with naloxone, prazosin, yohimbine, ketanserin, L-arginine, and parachlorophenylalanine (PCPA). HeCA produced dose-dependent and time course decrease in carrageenan-induced paw oedema. Pre- and post-treatment of rats with HeCA ameliorated CFA-induced arthritis evidenced in the significant decrease in arthritic index comparatively similar to the effect of celecoxib. CFA- induced oxidative and nitrosative stress were attenuated by subchronic treatment with HeCA. Findings from this study shows that C. anisata possesses antinociceptive activity through possible interaction with opioidergic, noradrenergic, L-arginine-nitric oxide and serotonergic pathways as well as anti-arthritic property which could be attributed to its ability to prevent the release of inflammatory mediators and oxidative stress.
Referenser
Ahmad, S.F., Khan, B., Suri, K.A., Satti, N.K., Qazi, G.N. (2006). Amelioration of adjuvant- induced arthritis by ursolic acid through altered Th1/Th2 cytokine production. Pharmacol Resources 53: 233-240.
Ajibesin, K. K., Ekpo, B.A., Bala, D.N., Essien, E.E., Adesanya, S.A. (2008). Ethnobotanical survey of Akwa Ibom State of Nigeria. J Ethnopharmacol 115: 387-408.
Alchaider, A.A. 1991. Antinociceptive effect of ketanserin in mice: involvement of supraspinal 5-HT2 receptors in nociceptive transmission. Brain Res, 543,335-40.
Alves, P.D., Tatuso, Maria, A.F., Romulo-Leite-Duarte DG. (2004). Diclofenac-induced peripheral antinociception is associated with ATP-sensitive K+ channels activation. Life Sci 74, 2577-91.
Amoo SO, Aremu AO, Moyo M, Van Staden J. 2013. Assessment of long-term storage on antimicrobial and cyclooxygenase-inhibitory properties of South African medicinal plants. PhytotherRes. 27(7):1029-35.
Anburajan, M., Snekhalatha, U., Venkatraman, B., Menaka, M. (2012). Evaluation of complete Freund’s adjuvant-induced arthritis in a Wistar rat model. Rheumatol 8: 21-46.
Arbab, I.A., Abdul, A.B., Aspollah M., Abdullah, R., Abdelwahab SI, Ibrahim, M.Y., Ali, L.Z. 2012. A review of traditional uses, phytochemical and pharmacological aspects of selected members of Clausena genus (Rutaceae). J Med Plants Res, 6(38), 5107-5118.
Awodele O, Ishola IO, Ikumawoyi VO, Akindele AJ, Akintonwa A. 2013. Toxicological evaluation of the lyophilized fruit juice extract of Annona muricata Linn. (Annonaceae) in rodents. J Basic Clin Physiol Pharmacol, 18:1-11.
Bamgbose, S.O., Noamesi, B.K. (1981). Studies on crytolepine II: inhibition of carrageenan- induced oedema by Crytolepine. PlantaMedica. 42:392-396.
Cury Y, Picolo G, Gutierrez VP, Ferreira SH. 2011. Pain and analgesia: The dual effect of nitric oxide in the nociceptive system. Nitric Oxide, 25(3):243-54.
Edwards G, Weston AH. 1993. The pharmacology of ATP-sensitive potassium channels. Ann Rev Pharmacol Toxicol, 33: 597-637.
El-Olemy MM, Al-Muhtadi FJ, Afifi AA. A Laboratory Manual. Riyadh, Saudi Arabia: King Saud University Press; 1994. Exper Phytochem; pp. 3-137.
Gundidza, M., Chiyangaya, F., Chagonda, L., Depooter, H.L., Mavi, S. (1994). Phytoconstituents and antimicrobial activity of the leaf essential oil of Clausena anisata (Wild) Hook. F. ex Benth. Flavour Fragrance J 9: 299-303.
Harbone JB. London: Chapman and Hall Ltd; (1973). Phytochemical methods; pp. 148-89.
Ishola, I.O., Agbaje, E.O, Adeyemi, O.O., Shukla, R. (2014a). Analgesic and anti-inflammatory effects of the methanol root extracts of some selected Nigerian medicinal plants. Pharm Biol, 52(9):1208-16.
Ishola I.O., Agbaje, E.O., Akinleye, M.O., Ibeh C.O., Adeyemi, O.O. (2014b). Antidepressant-like effect of the hydroethanolic leaf extract of Alchornea cordifolia (Schumach. &Thonn.) Mull. Arg. (Euphorbiaceae) in mice: Involvement of monoaminergic system. J Ethnopharmacol, http://dx.doi.org/10.1016/i.iep.2014.10.008.
Ishola IO, Akindele AJ, Adeyemi OO. (2011). Analgesic and anti-inflammatory activities of Cnestis ferruginea Vahl ex DC (Connaraceae) methanolic root extract. J Ethnopharmacol, 26, 135(1):55-62.
Ito C, Itoigawa M, Aizawa K, Yoshida K, Ruangrungsi N, Furukawa H (2009). Gamma-lactone carbazoles from Clausena anisata. J Natural Prod 72:1202-1204.
Kaur, R., Singh, D., Chopra, K. (2005). Participation of alpha-2 receptor in the antinociceptive activity of quercetin. J Med Food, 8, 529-32.
Knight AR, Misra A, Quirk K, Benwell K, Revell D, Kennett G, Bickerdike M (2004) Pharmacological characterisation of the agonist radioligand binding site of 5-HT2A, 5-HT2B and 5-HT2C receptors. Naunyn Schmiedebergs Arch Pharmacol, 370:114-123.
Kokkola R, Li J, Sundberg E, Aveberger A.C., Palmblad K., Yang H., Tracey K.J., Andersson U, Harris H.E. (2003). Successful treatment of collagen-induced arthritis in mice and rats by targeting extracellular high mobility group box chromosomal protein 1 activity. Arthritis Rheumatol, 48(7):2052-8.
Liang, Y.C., Huang, Y.T., Tsau, S.H., Lin-Shiau, S.Y., Chen, C.F., Lin, J.K. (1999). Suppression of inducible cyclo-oxygenase and inducible nitric acid synthase by apigenia and related flavonoid in mouse macrophages. Carcinogenesis 20: 1945-1952.
Makanju, O.O.A. (1983). Behavioral anticonvulsant effect of an aqueous extract from the roots of Clausena anisata Rutaceae. Int J Crude Drug Res 21: 29-32.
Malmberg, A.B., Yarksh, T.l. (1992). Antinociceptive actions of spinal non-steroidal anti-inflammatory agents on the formalin test in the rat. J Pharmacol Exper Therapeut. 263(1):136- 146.
Meller S.T, Gebhart G.F. (1993). Nitric oxide (NO) and nociceptive processing in the spinal cord. Pain, 52(2):127-36
Millan, M.J. (2002) Descending control of pain. ProgNeurobiol, 66:355-474.
Moore PK, Oluyomi AO, Babbedge RC, Wallace P, Hart SL. 1991. L-NG-nitro arginine methyl ester exhibits antinociceptive activity in the mouse. Br J Pharmacol, 102(1):198-202.
Morgan CV, Babbedge RC, Gaffen Z, Wallace P, Hart SL, Moore PK. (1992). Synergistic anti-nociceptive effect of L-NG-nitro arginine methyl ester (L-NAME) and flurbiprofen in the mouse. Br J Pharmacol, 106(2):493-7.
Nakahara, K., Trakoontivakorn, G., Alzoreky, N. S., Ono, H., Onishi- Kameyama, M., Yoshida, M. (2002). Anti-mutagenicity of some edible Thai plants and a bioactive carbazole alkaloid, Mahanine, isolated from Micremelum minutum. Journal of Agricultural and Food Chemistry. 50: 4796- 4802
Ojewole, J.A. (2002). Hypoglycemic effect of Clausena anisata (Wild). Hook. F. ex Benth. methanol root extract in rats. JEthnopharmacol 81: 231-237.
Pertovaara, A. (2013). The noradrenergic pain regulation system: a potential target for pain therapy. Eur J Pharmacol, 716(1-3): 2-7.
Rajendran, N.N., Thirugnanasambantham, P., Viswanathan, S., Parvathavarthini, S., Ramaswamy, S. (2000). Antinociceptive pattern of flavone and its mechanism as tested by formalin assay. Indian J Exp Biol, 38, 82-5.
Senguttuvan J, Paulsamy S, Karthika K. (2014). Phytochemical analysis and evaluation of leaf and root parts of the medicinal herb, Hypochaeris radicata L. for in vitro antioxidant activities. Asian Pacific J Trop Biomed, 4(Suppl 1):S359-67.
Senthikumar, A., Venkatesalu, V. (2009). Phytochemical analysis and antibacterial activity of essential oil of Clausena anisata (Wild). Hook. F. ex Benth. Internal J Integrative Biol 5: 116 - 120.
Suzuki R, Rygh LJ, Dickenson AH (2004). Bad news from the brain: descending 5-HT pathways that control spinal pain processing. Trends Pharmacol Sci, 25:613-617.
Usman, L.A., Hamid, A.A., Olawore, N.O., Fakunle, C.O., Oladosu, L.A., Zunbair, M.F. (2010). Chemical composition of leaf essential oil of Clausena anisata growing in North-Central Nigeria. J Applied Sci Res 6: 891-894.
Vane, T., Booting, R., (1987). Inflammation and mechanism of action of anti-inflammatory drugs. Fed Am Soc Exp Biol J 1: 89-96.
Verma, P.R., Joharrapurkar, A.A., Chaptplliwar, V.A., Asnani, A.J. (2005). Antinociceptive activity of alcoholic extract of Hermidesmus indicus in mice. J Ethnopharmacol. 102(2): 298¬301.
Zakaria, Z.A., Hazalin, N.A.M., Zaid, S.N. (2007). Antinociceptive, anti-inflammatory and anti pyretic effects of Muntigia calabura aqueous extract in animal models. J Natural Med. 61(4): 443-448., lack of central analgesia and antipyretic propertiesof Acanthus montanus (Ness) T. Anderson. J. Ethnopharmacol. 95:63-68.
Carney, J. A. and Rosomoff, R. N. (2009) In the Shadow of Slavery. Africa’s Botanical legacy in the Atlantic World. Berkeley: University of California Press
Chakraborty A, Devi, R.K., Rita, S., Sharatchandra, K. and Singh T.I. (2004). Preliminary studies on antiinflammatory and analgesic activities of Spilanthes acmella in experimental animal models. Indian J. Pharmacol. 36:148-50.Domer, F. (1990). Characterization of the analgesic activity of Ketorolac in mice. Europ. J. Pharmacol. 177: 127-135.
Drozdova, I.L. and Bubenchikov, R.A. (2005). Composition and anti-inflammatory activity of polysaccharide complexes extracted from sweet violet and low mallow. Pharm. Chem. J. 39: 197-200.
Duke, J.A. 1981. The gene revolution. Paper 1. p. 89–150. In: Office of Technology Assessment, Background papers for innovative biological technologies for lesser developed countries. USGPO. Washington
Ezike, A.C., Akah, P.A., Okoli, C.C. and Okpala, C.B. (2010). Experimental evidence for the antidiabetic activity of Cajanus cajan leaves in rats. J. Basic Clin. Pharm.1:25–30.
Fields, H.L. (1987). Analgesic Drugs. In: Day W, ed. Pain. MacGraw- Hill, USA. pp 272.
Fuller, D.Q. and Harvey, E. (2006). The archaeobotany of Indian Pulses: identification, processing and evidence for cultivation. Environ. Arch. 11(2), 219-246.
García, M.D., Fernández, M.A., Alvarez A. and Saenz, M.T. (2004). Antinociceptive and anti-inflammatory effect of the aqueous extract from leaves of Pimenta racemosa var. ozua (Mirtaceae). J. Ethnopharmacol. 91: 69–73.
Kong, Y., Fu, Y.J., Zu, Y.G., Chang, F.R., Chen, Y.H., Liu, X.L., Stelten, J. and Schiebel, H.M. (2010). Cajanuslactone a new coumarin with anti bacterial activity from pigeon pea leaves. Food Chem. 121:1150–5.
Lorke, D. (1983). A New Approach For Acute Toxicity Testing. Arch. Toxicol. 54: 275-287
Luo, M., Liu, X., Zu, Y., Fu, Y., Zhang, S., Yao, L. and Efferth, T. (2010). Cajanol, a novel anticancer agent from Pigeon pea [Cajanus cajan (L.) Millsp.] roots, induces apoptosis in human breast cancer cells through a ROS mediated mitochondrial pathway. Chem Biol Interac. 188:151–60.
Luo, Q.F., Sun, L., Si, J.Y. and Chen, D.H. (2008). Hypocholesterolemic effect of stilbenes containing extract fraction from Cajanus cajan on diet induced hypercholesterolemia in mice. Phytomedicine. 15:932–9.
Morton, J.F. (1976). The pigeon pea (Cajanus cajan Millsp.), a high protein tropical bush legume. Hort Sci.11:11–9.
Nicholson, R.A., David, L.S., Pan, R.L. and Liu, X.M. (2010). Pinostrobin from Cajanus cajan (L.) Millsp. Inhibits sodium channel-activated depolarization of mouse brain synaptoneurosomes. Fitoterapia. 81:826–9.
OECD. 1987. Test No. 402. Acute Dermal Toxicity [adopted 24 February 1987]. In: OECD Guidelines for the Testing of Chemicals, Section 4: Health Effects. Paris:OECD Publishing. Available: http://dx.doi.org/10.1787/9789264070585-en
Okoli, C.O., Njoku, O.U., Ononogbu, I.C. and Ezike, A.C. (2007). Medicinal plants and antioxidant activity. In: Principles and Practice of Ethnomedicine (African Approach). Edited by Akah P.A, India. Research Signpost. In- press.
Olajide, O.A., Makinde, J.M., Okpako, D.T. and Awe, S.O. (2000). Studies on the anti-inflammatory and related pharmacological properties of the aqueous extract of Bridelia ferruginea stem bark. J. Ethnopharmacol. 71: 153-160.
Oloyede, A.M., Okpuzor, J., Omidiji, O. and Mbagwu, H.O.C. (2008) A pharmacological
evaluation of a herbal cocktail. Intern. J. Pharmacol. 4(3): 196-201.
Oridupa, O.A. and Saba A.B. (2012). Relative anti-inflammatory and analgesic activities of the whole fruit, fruit bark, pulp and seed of Lagenaria breviflora Roberty. J. Pharmacol. Toxicol. 7(6): 288 -297.
Pal, D., Mishra, P., Sachan, N. and Ghosh, A.K. (2011). Biological activities and medicinal properties of Cajanus cajan (L) Millisp. J. Adv. Pharma. Technol. Res. 2(4): 207-214
Peter, P.I. (2008). Leaf and non-leaf vegetables: Food for wellness. In: Total Wellness Series 3, Peter K.V. (ed) World Wellness Open University, Chennai, India. Pp 116 – 118.
Peters, R.R., Saleh, T.F., Lora, M., Patry, C., de Brum-Fernandes, A.J. and Ribeiro-do-Valle, R.M. (1999). Anti-inflammatory effects of the products from Wilbrandia ebracteata on carrageenan-induced pleurisy in mice. Life Sci. 64 (26): 2429 -2437.
Ramabadran, K., Bansinath, M., Turndorf H. and Puig, M.M. (1989). Tail immersion test for the evaluation of a nociceptive reaction in mice: Methodological consideration. J. Pharmacol. Methods. 21: 21-31.
Singh, S., Mehta, A., John, J. and Mehta, P. (2010). Anthelmintic potential of Andrographis paniculata, Cajanus cajan and Silybum marianum. Pharmacog. J. 2:71–3.
Tjolsen, A., Gerge, O.G., Hunskaar, S., Rosland, J.H. and Hole, K. (1992). The formalin test: an evaluation of method. Pain 51: 3-17.
Zeashana, H., Amresha, G. Raoa C.V. and Singhb, S. (2009). Antinociceptive activity of Amaranthus spinosus in experimental animals. J. Ethnopharmacol. 122: 492–496.
Zhang, D.Y., Zhang, S., Zu, Y.G., Fu, Y.J., Kong, Y., Gao, Y., Zhao, J.T. and Efferth, T. (2010). Negative pressure cavitation extraction and antioxidant activity of genistein and genistin from the roots of pigeon pea. Sep. Purif. Tech. 74: 261–70.
Nedladdningar
Publicerad
Nummer
Sektion
Licens

Detta verk är licensierat under en Creative Commons Erkännande-Ickekommersiell-IngaBearbetningar 4.0 Internationell-licens.