BMC Complementary and Alternative Medicine | |
Pharmacological evidence for the folk use of Nefang: antipyretic, anti-inflammatory and antinociceptive activities of its constituent plants | |
Anastasia N. Guantai2  Gabriel A. Agbor1  Jackson Mugweru3  Amos M. Mwaura2  William N. Ngugi2  Juma D. Siminyu2  Faith A. Okalebo2  Protus Arrey Tarkang2  | |
[1] Centre for Research on Medicinal Plants and Traditional Medicine, Institute of Medical Research and Medicinal Plants Studies (IMPM), Yaoundé, Cameroon;Department of Pharmacology and Pharmacognosy, School of Pharmacy, University of Nairobi, Nairobi, Kenya;Department of Veterinary Anatomy and Physiology, Faculty of Veterinary Medicine, University of Nairobi, Nairobi, Kenya | |
关键词: Antinociceptive activities; Anti-inflammatory; Antipyretic; Pharmacological effects; Nefang; Medicinal plants; | |
Others : 1212017 DOI : 10.1186/s12906-015-0703-7 |
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received in 2014-11-14, accepted in 2015-05-29, 发布年份 2015 | |
【 摘 要 】
Background
Nefang is a polyherbal anti-malarial composed of Mangifera indica (MiB and MiL ; bark and leaf), Psidium guajava (Pg), Carica papaya (Cp), Cymbopogon citratus (Cc), Citrus sinensis (Cs) and Ocimum gratissimum (Og) (leaves). Previous studies have demonstrated its in vitro and in vivo antiplasmodial activities, antioxidant properties and safety profile. This study aimed at evaluating the antipyretic, anti-inflammatory and antinociceptive activities of the constituent plants of Nefang which are relevant to the symptomatic treatment of malaria fever.
Methods
Antipyretic activities were determined by the D-Amphetamine induced pyrexia and Brewer’s Yeast induced hyperpyrexia methods. Anti-inflammatory activities were investigated using the carrageenan-induced rat paw edema method. Antinociceptive activities were determined by mechanical nociception in the tail pressure and thermal nociception in the radiant heat tail flick and hot plate methods. Data was analysed using the one way ANOVA followed by Neuman-Keuls multiple comparison test.
Results
Best percentage inhibition of induced pyrexia (amphetamine/brewer’s yeast; p < 0.05) was exhibited by Cc (95/97) followed by Og (85/94), MiL (90/89), MiB (88/84) and Cs (82/89). Cc and Og exhibited comparable activities to paracetamol (100/95).
Anti-inflammatory studies revealed paw edema inhibition (%) as follows (p < 0.05): Indomethacin (47), MiL (40), Cp (30), MiB (28) and Og (22), suggesting best activity by MiL.
Antinociceptive studies revealed significant (p < 0.01) pain inhibition (%) as follows: Paracetamol (97), Og (113), MiL (108), Pg (84) and MiB (88). Og and MiL exhibited the best activities.
Conclusion
The results obtained suggest that the constituent plants possess biologically active compounds with antipyretic, anti-inflammatory and antinociceptive activities. These activities are essential in the symptomatic treatment of malaria fever, thereby justifying the folk use of Nefang. This would be useful in its subsequent development for clinical application.
【 授权许可】
2015 Tarkang et al.
【 预 览 】
Files | Size | Format | View |
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Fig. 1. | 27KB | Image | download |
【 图 表 】
Fig. 1.
【 参考文献 】
- [1]Snow RW, Marsh K. Malaria in Africa: progress and prospects in the decade since the Abuja Declaration. Lancet. 2010; 376:137-9.
- [2]WHO. World Malaria Report 2013. World Health Organization, Geneva. http://www.who.int/malaria/publications/world_malaria_report_2013/en/.
- [3]Emergency response to artemisinin in the greater Mekong sub-region: regional framework for action 2013-2015. WHO 2013. http://www.who.int/malaria Resistance in GMS Summary Report.
- [4]World Health Organization. Traditional medicine. Fact sheet No. 134. 2003. http://www.who.int/mediacentre/factsheets/2003/fs134/en/.
- [5]Oliveira AB, Dolabela MF, Braga FC, Jacome RL, Varotti FP, Povoa MM. Plant-derived antimalarial agents: new leads and efficient phythomedicines. Part I. Alkaloids. An Acad Bras Cienc. 2009; 81:715-40.
- [6]Castellanos JRG, Prieto JM, Heinrich M. Red Lapacho (Tabebuia impetiginosa)– a global ethnopharmacological commodity? J Ethnopharmacol. 2009; 121:1-13.
- [7]Ginsburg H, Deharo E. A call for using natural compounds in the development of new antimalarial treatments - an introduction. Malar J. 2011; 10 Suppl 1:S1. BioMed Central Full Text
- [8]Tarkang PA, Okalebo FA, Agbor GA, Tsabang N, Guantai AN, Rukunga GM. Indigenous knowledge and folk use of a polyherbal antimalarial by the Bayang community, South West Region of Cameroon. J Nat Prod Plant Res. 2012; 2(3):372-80.
- [9]Tarkang PA, Atchan APN, Kuiate J, Okalebo FA, Guantai AN, Agbor GA. Antioxidant potential of a polyherbal antimalarial as an indicator of its therapeutic value. Adv Pharmacol Sci. 2013; 2013:678458.
- [10]Tarkang PA, Franzoi KD, Lee S, Lee E, Vivarelli D, Freitas-Junior L, Liuzzi M, Tsabang N, Ayong LS, Agbor GA, Okalebo FA, Guantai AN. In vitro antiplasmodial activities and synergistic combinations of differential solvent extracts of the polyherbal product. Nefang BioMed Res Int. 2014; 2014:835013.
- [11]Tarkang PA, Okalebo FA, Ayong LS, Agbor GA, Guantai AN. Anti-malarial activity of a polyherbal product (Nefang) during early and established Plasmodium infection in rodent models. Malar J. 2014; 13:456. BioMed Central Full Text
- [12]Mbagwu HO, Anene RA, Adeyemi OO. Analgesic, antipyretic and anti-inflammatory properties of Mezoneuron benthamianum Baill Caesalpiniaceae. Niger Quart J Hosp Med. 2007; 17(1):35-41.
- [13]Turner RA. Screening method in Pharmacology. Academic, New York & London; 1965.
- [14]Mohamed-Saleem TK, Azeem AK, Dilip C, Sankarl C, Prasanth NV, Duraisami R. Anti-inflammatory activity of the leaf extracts of Gendarussa vulgaris Nees. Asian Pac J. Trop Biomed 2011, 1(2):147-149.
- [15]Randall LO, Selitto JJ. A method for measurement of analgesic activity on inflamed tissue. Arch Int Pharmacodyn. 1957; 111:409-19.
- [16]Kitchen I. Modification of an analgesy meter for paw pressure antinociceptive testing in neonatal rats. J Pharmacol Meth. 1984; 12:255-8.
- [17]Ramesh R. Analgesic Effects of the aqueous extracts of plant Ipomea pes-tigridis studied in albino mice. Global J Pharmacol. 2010; 4(1):31-5.
- [18]Janssen PAJ, Jagenea AH. A new series of potent analgesics: Dextro 2,2-diphenyl-3 methyl- hmorholino- butryprolidine and related amides. Part 1. Chemical structure and pharmacological activity. J Pharm. 1957; 9:38.
- [19]Gupta M, Mazumder UK, Kumar RS, Gomathi P, Rajeshwar Y, Kakoti BB, Selven VT. Anti-inflammatory, analgesic and antipyretic effects of methanol extract from Bauhinia racemosa stem bark in animal models. J Ethnopharmacol. 2005; 98(3):267-73.
- [20]Okokon JE, Nwafor PA, Abia GO, Bankhede HK. Antipyretic and antimalarial activities of crude leaf extract and fractions of Enicostema littorale. Asian Pac J Trop Dis. 2012; 2(6):442-7.
- [21]Al-Ghamdi MS. The anti-inflammatory, analgesic and antipyretic activity of Nigella sativa. J Ethnopharmacol. 2001; 76:45-8.
- [22]Westfall TC, Westfall DP. Goodman and Gilman’s the pharmacological basis of therapeutics. 2nd ed. Brunton LL, Chabner BA, Knollman BC, editors. McGraw-Hill Companies, New York, USA; 2011: p.277-334.
- [23]Chandrasekharan NV. COX-3, a cyclooxygenase-1 variant inhibited by acetaminophen and other analgesic/antipyretic drugs: cloning, structure and expression. Proceedings National Acad Sci. 2002; 99:13926-31.
- [24]Rang HP, Dale MM, Ritter JM, Moore PK. Pharmacology. 6th ed. Churchill Livingstone, Edinburgh; 2007.
- [25]Crunkhon P, Meacock SER. Mediators of the inflammation induced in the rat paw by carrageenan. Brit J Pharmacol. 1971; 42:392-402.
- [26]Georgewill OA, Georgewill UO. Evaluation of the anti-inflammatory activity of extract of Vernonia Amygdalina. Asian Pac J Trop Med. 2010; 3(2):150-1.
- [27]Chindo BA, Amos S, Odutola AA, Vongtau HO, Abah J, Wambebe C, Gamaniel KS. Central nervous system activity of the methanolic extract of Ficus platyphylla stem bark. J Ethnopharmacol. 2003; 85:131-7.
- [28]Vongtau HO, Abbah J, Mosugu O, Chindo BA, Ngazal IE, Salawu AO, Kwanashie HO, Gamaniel KS. Antinociceptive profile of the methanolic extract of Neorautanenia mitis root in rats and mice. J Ethnopharmacol. 2004; 92(2 & 3):317-24.
- [29]Tjølsen A, Berge O, Hunskaar S, Rosland JH, Hole K. The formalin test; an evaluation of the method. Pain. 1992; 51:5-17.
- [30]Eaton DC, Pooler JP. Vander’s Physiology. 7th ed. McGraw-Hill Lange, USA; 2009.
- [31]Gege-Adebayo GI, Bassi AS, Igbokwe VU, Shafe MO. Antipyretic effect of Ocimum gratissium on brewer’s yeast induced fever in wistar rats. J Medicine Medical Sc. 2013; 4(6):247-51.
- [32]Ojewole JA. Anti-inflammatory, analgesic and hypoglycemic effects of Mangifera indica Linn. (Anacardiaceae) stem-bark aqueous extract. Methods Find Exp Clin Pharmacol. 2005; 27(8):547-54.
- [33]Olorunfemi OJ, Nworah DC, Egwurugwu JN, Hart VO. Evaluation of anti-inflammatory, analgesic and antipyretic effect of Mangifera indica leaf extract on fever-induced albino rats (wistar). British J Pharmacol Toxicol. 2012; 3(2):54-7.
- [34]Sagnia B, Fedeli D, Casetti R, Montesano C, Falcioni G, Colizzi V. Antioxidant and anti-Inflammatory activities of extracts from Cassia alata, Eleusine indica, Eremomastax speciosa, Carica papaya and Polyscias fulva medicinal plants collected in Cameroon. PLoS One. 2014; 9(8):e103999.
- [35]Ojewole JAO. Anti-inflammatory and analgesic effects of Psidium guajava Linn. (Myrtaceae) leaf aqueous extracts in rats and mice. Methods Find Exp Clin Pharmacol. 2006; 28(7):441-6.