Antiplasmodial Activity of Methanolic Leaf Extract of Daniella oliveri in Albino Mice Infected with Plasmodium berghei Nk 65

https://dx.doi.org/10.4314/njpar.v42i2.28

Authors

  • Dikwa K. B Department of Biological Sciences, Nigerian Defense Academy Kaduna
  • Dibal D. M Pharmacology Laboratory, College of Health Sciences, Kogi State University, Anyigba
  • Muazu M Pharmacology Laboratory, College of Health Sciences, Kogi State University, Anyigba
  • Obaje G Department of Medical Biochemistry, College of Health Sciences, Kogi State University, Anyigba

Keywords:

curative, antiplasmodial, methanolic, Daniella oliveri

Abstract

Human malaria is a life-threatening disease caused by 5 species of plasmodia. Qualitative, quantitative and Gas Chromatography-Mass Spectrometry (GC-MS) analysis was used to determine some bioactive components used in accessing the antiplasmodial potentials of methanolic leaf extract of Daniella oliveri in mice. Twenty-five (25) albino mice of body weight between 18-25 g were randomized into 5 groups of five mice per group for acute toxicity test, while for antiplasmodial studies. Thirty (30) mice were randomized to 6 groups of 5 mice per group (groups 1, 2, 3, 4, 5 and 6). The mice were Infected intravenously with 0.2 ml of 1x107 standard inoculum of chloroquine sensitive Plasmodium berghei infected erythrocytes on the first day (day 0).72 hours later (day 3), 0.2 ml of 200, 400 and 800 mg/kg body weight of leaf extract were administered orally to mice in groups 4, 5 and 6 respectively as treatment dose once daily for 5 consecutive days. Group 1 (positive control) were treated with 0.2 ml of 5 mg/kg body weight of chloroquine, group 2 (negative control) were given 0.2 ml of normal saline and group 3 (normal control) received 0.2 ml of normal saline but were not infected with P. berghei. Blood samples were collected from all mice in all groups for the determination of percentage Parasitemia and chemo-suppression through vene-section of the tail. The qualitative Phytochemical analysis revealed the presence of Alkaloids, Flavonoids, Tannins, Cardiac glycosides, Reducing sugar, Saponins, Terpernoids, Phenols. The GC-MS analysis revealed 57 chemicals. The highest dose 800mg/kg body weight showed a very good antiplasmodial activities with a significant decrease (P<0.05). Daniella oliveri have displayed to be a potentially “very good’’human antimalarial medicinal plant.

Purchase

 

Author Biographies

Dibal D. M, Pharmacology Laboratory, College of Health Sciences, Kogi State University, Anyigba

Department of Biological Sciences, Nigerian Defense Academy Kaduna

 

Muazu M, Pharmacology Laboratory, College of Health Sciences, Kogi State University, Anyigba

Department of Biological Sciences, Nigerian Defense Academy Kaduna

 

References

Dada, E. O. and Muhammed, D. (2018). Effect of Ethanolic Leaf Extract of Eucalyptuscitriodora Hookon Haematological Parameters of Swiss Albino Mice Infected with Plasmodium berghei NK 65. South Asian Journal of Parasitology. 1(2): 1-8.

World Health Organisation (2018). ‘Malaria: Fact Sheet.

World Health Organization (2015). Fact sheet. World Malaria report. Retrieved from http://www.who.int/ malaria/media/world-malaria-report 2015.

Ogundolie, O.O., Dada, E. O., Osho, I. B. and Oloruntola, D. A. (2017). Effect of Raw Ethanolic Seed Extract of Tetracarpidium conophorum on Heamatological Parameters in Swiss Albino Mice Infected with P. berghei. Journal of Applied Life Sciences International, 12 (2): 1103-234.

Joint WHO/UNICEF news release report: Malaria MDG target achieved amid sharp drop in cases and mortality, but 3 billion people remain at risk, 2015. Available at www.who/ int./ media centre/ news/releases/ 2015/ malaria-mdg-target/ en/.

World Health Organization (2019). World Malaria Report; 2019. pp. xii–xiii, 4–10. ISBN 97892-4-156572-1.

Awoke, N and Arota, A. (2019). Profile of hematological parameters in Plasmodium falciparum and Plasmodium vivax malaria patients attending Tercha General Hospital, Dawuro Zone, South Ethiopia. Infection and Drug Resistance 12:521-527.

Garba, D.D., Ameh, B.J., Whong, Z.M.C., Aminu-Mukhtar, M.(2016). Prevalence of malaria parasites among blood donors in Kaduna, Nigeria. International Journal of Research in Medical Sciences. 4(6):2320- 6071.

Maimuna, B.U., Emmanuel O.O., Josephine, Y.I., Oluwakanyinsola, A.S., Adeniyi, Y.T., Ibrahim, M.H. (2013). Antiplasmodial Efficacy of Methanolic Root and Leaf Extracts of Morinda lucida, Journal of Natural Sciences Research. 3(2): 2225-0921.

Federal Ministry of Health (FMOH) (2005). National Antimalarial Treatment Guidelines. Federal Ministry of Health. National Malaria and Vector Control Division.Abuja-Nigeria.

World Health Organization (2011). World malaria reports WHO/UNICEF, Geneva. Retrieved February 2021, from http://www.who.intimalaria/world malaria report_2011.

Centre for disease control and prevention (CDC)/United States agency for international Development (USAID), (2012). President’s Malaria Initiative. Economic Section, United State Embassy in Nigeria. Federal Capital Territory (FCT). Abuja, Nigeria. http: //nigeria.usembassy.gov

World Health Organization (2017). Global Vector Control Response. World Heal. Organ.Accessed on Jan 2021.

Hosseinzadeh, S., Jafarikukhdan, A., Hosseini, A. and Armand, R. (2015). The Application of Medicinal Plants in Traditional and Modern Medicine: A Review of Thymus vulgaris. International Journal of Clinical Medicine,6: 635-642.

Hutchinson, J., & Dalziel, J. M. (1963). Flora of West Tropical African; Vol. 2, Crown Agents, London. 16. Muhammad, M. I. , (2017). A pharmacognostical efficacy of five plants traditionally used for the treatment of cancer in Northern Nigeria. Retrieved March 15, 2020, from http://docs.edu.tr/library/ 6502099512.

Al-Harrasi, A. Al-Rawahi, A., Hussain, J., Rehman, N., Ali, L. and Hussain H. (2012). Proximate analysis of the resins and leaves of Boswellia sacra. J Med Plants Res. 6 (16):3098-3104.

Temitope O.O., Fasusi, O.A., Ogunmodede, A.F., Thonda, A.O., Oladejo, B.O., Yusuf-Babatunde, A.M. and Ige, O.O. (2016). Phytochemical Composition and Antimicrobial Activity of Daniella oliveri Extracts on Selected Clinical Microorganisms. International Journal of Biochemistry Research and Review 14(1): 1- 13.

Igoli, J.O., Ogaji, O.G., Tor-Anyiin, T.A. and Igoli, N.P., (2005). Traditional Medicine Practice Amongst the Igede People of Nigeria. Part II. Afri. J. Trad. Cam. 2(2):134- 152.

Dada, E.O. and Oloruntola, D.A. (2016). In vivo Antiplasmodial Activity of Ethanolic Leaf Extract of Tithonia diversifolia (Hemsl.) A. Gray Against P. berghei NK65 in Infected Swiss Albino Mice. Journal of Applied Life Science International, 8 (3): 1- 8.

Dickson, A.M., Fred, O.C.N. and Eleojo, O. (2011). Phytochemical, antibacterial and toxicity studies of the aqueous extract of Euclayptus camaldulensis Dehnh. Asian Journal of Plant Science and Research. 1(3):1-10.

Sofowora, A. (1993). Screening plants for bioactive agents. Medicinal plants and traditional medicinal in Africa. Ibadan: Spectrum Books.

Trease GE, Evans WC (1989). Textbook of pharmacognosy. 14. London: W.B. Sanders.

Harborne J.B. (1973). Phytochemical methods: a guide to modern techniques of plant analysis. 2. London: Chapman and Hall Publishers.

Muhammed, M., Dada, E.O. and Alo, A.A. (2018). Antibacterial Property of Ethanolic Leaf Extract of Eucalyptus citriodora Hook on Clinical and Typed Isolates of Escherichia coli. South Asian Journal of Research in Microbiology, 2(1): 1-8.

Basir, R., Rahiman, S. F. and Hasballah, K. (2012). P. berghei ANKA Infection in ICR Mice as a Model of Cerebral Malaria. Iran Journal of Parasitology, 7 (4): 62-74.

Alo, A.A., Dada, E.O. and Muhammed, D. (2018). Phytochemical Screening and Antiplasmodial Activity of Ethanolic Bark Extract of Khaya grandifoliola in Swiss Albino Mice Infected with Plasmodium berghei NK65. South Asian Journal of Parasitology, 1(4): 1-8.

Ryley, J.F and Peters, W (1970). The antimalaria activity of some quinolone esters. Am. Trop. Med. Parasitol. 84:209-222.

Kahn, M.E, Amupitan, J.O, Oyewale, A.O and Ndukwe, I.G., (2015). Evaluation of the In vivo Antimalarial activity of the methanolic leaf extract of Nepata cateria, Research in Pharmaceutical Biotechnology, 6(12): 8-15.

Omeiza, Favour. O., Ademowo, George. O and Funmilola A. Ayeni (2020). RESEARCH Evaluation of in vivo antimalarial potential of omidun obtained from fermented maize in Ibadan, Nigeria, Malaria Journal, 19: 414 https://doi.org/10.1186/ s12936-020- 03486-0.

Olafadehan O.A, Oluwafemi R.A, Alagbe J.O. (2020).Performance, haematobiochemical parameters of broiler chicks administered Rolfe (Daniellia oliveri) leaf extract as an antibiotic alternative. Drug Discovery, 14(33), 135- 145.

Bankole, A. E, Adekunle, A.A, Sowemimo, A.A, Umebese, C. E, Abiodun, O. and Gbotosho, G.O (2016). Phytochemical screening and in vivo antimalarial activity of extracts from three medicinal plants used in malaria treatment in Nigeria, Parasitol Res. 2016; 115: 299–305.

Iwu C, Klayman DL. Evaluation of the in vitro antimalarial activity of Picralima nitida extracts. J Ethnopharmacol. 1992;36:133–135. doi: 10.1016/0378- 8741(92)90012 G.

Amoa Onguéné, P., Ntie-Kang, F., Lifongo, L.L. et al. (2013).The potential of antimalarial compounds derived from African medicinal plants. Part I: A pharmacological evaluation of alkaloids and terpenoids. MalarJ 12, 449. https://doi.org/10.1186/1475-2875-12-449.

Okunade, S. A., Olafadehan, O. A., & Isah, O. A. (2014). Fodder potential and acceptability of selected tree leaves by goats. Animal Nutrition and Feed Technology, 14(3), 489-498.

Craig Steven and Kuhn David D. (2019). Understanding Fish Nutrition, Feeds, and Feeding. Virginia corporative extension https://fisheries.tamu. edu/files/2019/01/FST-269.pdf.420-256.

Toma Alameyahu, Serawit Deyno, Abrham Fikru,Amelework Eyado andAndrew Beale (2015). In vivo antiplasmodial and toxicological effect of crude ethanolextract of Echinop Kebericho traditionally used in treatment of malaria in Ethiopia, Biomed Central, 14(1):196.

Hendek Ertop M, Bektaş M. (2018). Enhancement of bioavailable micronutrients and reduction of antinutrients in foods with some processes. Food Heal; 4(3): 159 - 5 . [http://dx.doi.org/10.3153/FH18016].

Sowunmi A, Gbotosho GO, Adedeji AA, Fateye BA, Sabitu MF and Happi CT. Res. (2007). Effects of acute Plasmodium falciparum malaria on body weight in children in an endemic area. Parasitol. 101:343–49. PMID: 17323138.

Naria Mohandas and Xiuli An (2012). Malaria and Human Red Blood Cells. Medical Microbiol and Immunol (4):593- 598.

White, N.J.(2018). Anaemia and malaria. Malaria Journal. 17, 371. https: //doi.org/10.1186/s12936-018-2509-9.

Misganaw, D., Engidawork, E. & Nedi, T. (2019). Evaluation of the anti-malarial activity of crude extract and solvent fractions of the leaves of Olea europaea (Oleaceae) in mice. BMC Complement Altern Med 19, 171. https://doi.org/10.1186/s12906-019-2567-8.

Rasoanaivo P, Deharo E, RatsimamangaUrverg S, Frappier F (2004). Guidelines for the non clinical evaluation of the efcacy of traditional antimalarials. In: Willcox M, Bodeker G, Raoanaivo P, editors. Traditional Medicinal Plants and Malaria. Boca-Raton: CRC; p. 225–70.

Muluye, A.B., Desta, A.G., Abate, S.K. (2019). Anti-malarial activity of the root extract of Euphorbia abyssinica (Euphorbiaceae) against Plasmodium berghei infection in mice. Malaria Journal; 18, 261. https://doi.org/10.1186/s12936- 019-2887-7.

Oketch-Rabah HA, Lemmich E, Dossaji SF, Theander TG, Olsen CE, Cornett C, Kharazmi A, Christensen SB. (1997) : Two new antiprotozoal 5-methylcoumarins from Vernonia brachycalyx. J Nat Prod, 60:458–461.

Published

2023-07-01

How to Cite

K. B, D., D. M, D., M, M., & G, O. (2023). Antiplasmodial Activity of Methanolic Leaf Extract of Daniella oliveri in Albino Mice Infected with Plasmodium berghei Nk 65: https://dx.doi.org/10.4314/njpar.v42i2.28. Nigerian Journal of Parasitology, 42(2), 411–421. Retrieved from https://njpar.com.ng/index.php/home/article/view/199

Similar Articles

You may also start an advanced similarity search for this article.