Methanol Extract of Ficus trigonata Stem Bark Demonstrated Antiplasmodial Activity in Mice
DOI:
https://doi.org/10.47419/bjbabs.v5i01.269Keywords:
Chemo-suppression, Ficus trigonata, Malaria,, Parasitemia and Plasmodium berghei, Packed Cell VolumeAbstract
Malaria, caused by Plasmodium parasites, remains a global health concern, with drug resistance complicating control efforts. Plant-derived compounds have emerged as potential antimalarial agents. This study explores the effectiveness of methanol extract of Ficus trigonata stem bark against Plasmodium berghei in a murine model. Thirty (30) adult mice used in this study were divided into 5 groups of 6 mice per group. Group A was inoculated with P. berghei and not treated which served as negative control. Group B was inoculated and treated with 10mg/Kg body weight of chloroquine (standard control). Groups C, D and E were inoculated with Plasmodium berghei and treated with the extract in doses of 100, 200 and 300 mg/kg body weight respectively. Parameters such as Packed cell volume (PCV) was measured by hematocrit technique, Parasitemia levels were monitored by microscopy, and Chemo-suppression activity was calculated to assess antiplasmodial potential. The in vivo murine model that was used enables efficient preliminary screening with good predictive validity. Ficus trigonata stem bark extract showed dose-dependent antiplasmodial activity in Plasmodium berghei-infected mice. All doses (100-300mg/kg) significantly (p<0.05) increased the level of packed cell volume on days 1-3 post-treatment. Parasitemia levels reduced significantly (p<0.05), with 300 mg/kg approaching chloroquine efficacy. Impressive dose-dependent chemo-suppression reached 85.68% with the highest F. trigonata stem bark extract dose by day 4, nearing the 94.16% standard drug activity. These findings highlight the extract's potential as an antimalarial agent and contribute to the search for alternative treatments.Metrics
Downloads
References
World Health Organization. WHO World. 2020;2020. doi.org/10.1163/9789004636774048.
Maiga FO, Wele M, Toure SM, Keita M, Tangara CO, Refeld RR. Artemisinin- based combination therapy for uncomplicated plasmodium falciparum malaria in mali: A systematic review and meta-analysis. Malaria Journal. 2021;20(1):356–356. doi.org/10.1186/s12936-021-03890-0.
Okon OE, Gboeloh LB, Ud SE. Antimalarial effect of combined extracts of the leaf of ficus exasperata and stem bark of anthocleista vogelii on mice experimentally infected with plasmodium berghei berghei (nk 65). Research Journal of Medicinal Plant. 2014;8:99–111. 10.3923/rjmp.2014.99.111.
Bekono BD, Ntie-Kang F, Onguéné PA, Lifongo LL, Sippl W, Fester K. The poten- tial of anti-malarial compounds derived from african medicinal plants: A review of pharmacological evaluations from 2013 to 2019. Malaria Journal. 2020;19(1):183–
doi.org/10.1186/s12936-020-03231-7.
Afifi WM, Ragab EA, Im AES, Atef A. Bioactivities and phytoconstituents of ficus trigonata. Journal of Pharmacognosy and Phytochemistry. 2014;3(4):178–84.
Falade MO, Akinboye DO, Gbotosho GO, Ajaiyeoba EO, Happi TC, Abiodun OO. In vitro and in vivo antimalarial activity of ficus thonningii blume (moraceae) and lophira alata banks (ochnaceae), identified from the ethnomedicine of the nigerian middle belt. Journal of Parasitology Research. 2014;p. 972853–972853. doi.org/10.1155/2014/972853.
Kotepui M, Phunphuech B, Phiwklam N, Chupeerach C, Duangmano S. Effect of malarial infection on haematological parameters in population near thailand- myanmar border. Malar J. 2014;13:218–218. doi.org/10.1186/1475-2875-13-218.
El-Hamed A, Yousef WF, Mazrou NS, Elkholy Y, El-Refaiy W, Elfeky AI, et al. Anticryptosporidium efficacy of olea europaea and ficus carica leaves extract in immunocompromised mice associated with biochemical characters and antioxida- tive system. Cells. 2021;10(9). 10.3390/cells10092419.
Girmaw F, Engidawork E. In vivo anti-malarial activity of the aqueous root extract of euclea divinorum hiern (ebenaceae) against plasmodium berghei anka. Evidence-Based Complementary and Alternative Medicine. 2022;2022:2640648– 2640648. doi.org/10.1155/2022/2640648.
Kumar S, Kapkoti DS, Mina PR, Gupta M, Kumar R, Kumar P. Effect of liquiritigenin on chloroquine accumulation in digestive vacuole leading to apoptosis-like death of chloroquine-resistant p. Falciparum. Phytomedicine. 2023;114:154738–154738. doi.org/10.1016/j.phymed.2023.154738.
Hemmer CJ, Holst F, Kern P, Chiwakata CB, Dietrich M, Reisinger EC. Stronger host response per parasitized erythrocyte in plasmodium vivax or ovale than in plasmodium falciparum malaria. Tropical Medicine &. International Health. 2006;11(6):817–840. doi.org/10.1111/j.1365-3156.2006.01635.x.
Dikasso D, Makonnen E, Debella A, Abebe D, Urga K, Makonnen W. In vivo anti- malarial activity of hydroalcoholic extracts from asparagus africanus lam. In mice infected with plasmodium berghei
Das K, Tiwari R, Shrivastava D. Techniques for evaluation of medicinal plant prod- ucts as antimicrobial agent: Current methods and future trends. Journal of medicinal plants research. 2010;4(2):104–115. 10.5897/JMPR09.030.
Ii S, Emmanuel A, Nok AJ. Antimalaria effect of the ethanolic stem bark extracts of ficus platyphylla. Journal of Parasitology Research. 2011;24. doi.org/10.1155/2011/618209.
Anigboro AA, Avwioroko OJ, Cholu CO. Phytochemical constituents, antimalar- ial efficacy, and protective effect of eucalyptus camaldulensis aqueous leaf extract in plasmodium berghei-infected mice. Prev Nutr Food Sci. 2020;25(1):58–64. 10.3746/pnf.2020.25.1.58.
Dibessa TT, Engidawork E, Nedi T, Teklehaymanot T. Antimalarial activity of the aqueous extract of the latex of aloe pirottae berger. (aloaceae) against plasmod- ium berghei in mice. Journal of Ethnopharmacology. 2020;255:112763–112763. doi.org/10.1016/j.jep.2020.112763.
Saltarelli R, Palma F, Gioacchini AM, Calcabrini C, Mancini U, Bellis D, et al. Phy- tochemical composition, antioxidant and antiproliferative activities and effects on nuclear DNA of ethanolic extract from an italian mycelial isolate of ganoderma lucidum. J Ethnopharmacol. 2019;231:464–73. doi.org/10.1016/j.jep.2018.11.041.
PC C, editor. Pathophysiology of plasmodium falciparum-infected erythrocytes and thiol- mediated antioxidant detoxification systems; 2015. 10.4172/2470- 6965.1000S1-003.
Mangal P, Mittal S, Kachhawa K, Agrawal D, Rath B, Kumar S. Analysis of the clin- ical profile in patients with plasmodium falciparum malaria and its association with parasite density. J Glob Infect Dis. 2017;9(2):60–65. 10.4103/0974-777X.201626.
Bwalya AG, Phiri P, Kaiser M, Tasdemir D. Evaluation of the in vitro antimalarial and malaria prophylactic activity of eight ficus species. Planta Med. 2011;77(12):16–16. 10.1055/s-0031-1282139.
Araka A, Ayibadinipre J. Potency of ficus exasparata leaf extract on albino mice infected with plasmodium berghei berghei. Greener Journal of Medical Sciences. 2023;13(1):69–73.
Yang X, Guo JL, Ye JY, Zhang YX, Wang W. The effects of ficus carica polysac- charide on immune response and expression of some immune-related genes in grass carp, ctenopharyngodon idella. Fish Shellfish Immunol. 2015;42(1):132–139. doi.org/10.1016/j.fsi.2014.10.037.
Chandana M, Anand A, Ghosh S, Das R, Beura S, Jena S. Malaria parasite heme biosynthesis promotes and griseofulvin protects against cerebral malaria in mice. Nature Communications. 2022;13(1):4028–4028. doi.org/10.1038/s41467- 022-31431-z.
Tajbakhsh E, Kwenti TE, Kheyri P, Nezaratizade S, Lindsay DS, Khamesipour
F. Antiplasmodial, antimalarial activities and toxicity of african medicinal plants: A systematic review of literature. Malaria journal. 2021;20(1):1–50. doi.org/10.1186/s12936-021-03866-0.
Kratchanova M, Denev P, Ciz M, Lojek A, Mihailov A. Evaluation of antioxidant activity of medicinal plants containing polyphenol compounds. Comparison of two extraction systems. Acta Biochim Pol. 2010;57(2):229–263. 20532255.
Downloads
Published
Issue
Section
Categories
License
Copyright (c) 2024 SULEIMAN MAHMOUD JADA, Yusuf Umar, Abdullahi Usman Wurochekke

This work is licensed under a Creative Commons Attribution 4.0 International License.
The authors retain all proprietary rights, including copyright, such as patent and trademark rights and rights to any process or procedure described in the article.

