Evaluation of antimalarial compounds in Prosopis africana stem bark fractions against Plasmodium berghei
DOI:
https://doi.org/10.55779/nsb16311795Keywords:
antimalarial potential, compound identification, fraction F5, Prosopis africana, superior activityAbstract
Prosopis africana, a traditional medicinal plant for malaria treatment, requires further scientific evidence. This study aimed to assess the antimalarial potential of Prosopis africana stem bark fractions in Plasmodium berghei-infected mice and identify the responsible compounds. The aqueous extract underwent partitioning with n-hexane, ethyl acetate, and methanol, followed by antimalarial evaluation. F5 was the most potent fraction based on its antimalarial potential. The study pooled 36 chromatographic separation sub-fractions into five using TLC analysis Rf values. In Plasmodium berghei-infected mice, fraction F5 at 6.25, 12.5, 25, and 50 mg/kg body weight (bw) was tested for antimalarial activity. Compound analysis of F5 utilized ultra-performance liquid chromatography-quadrupolar mass spectrometry. Statistical analysis employed Analysis of Variance and Duncan's multiple range tests (p < 0.05). The methanol, n-hexane, and ethylacetate extracts displayed suppression of P. berghei by 90%, 72.2%, and 73.6%, respectively. Methanol, n-hexane, and ethylacetate extracts suppressed P. berghei by 90%, 72.2%, and 73.6% respectively. F5 showed significantly higher chemo-suppression (67.21%) than F1 (63.94%), F2 (6.99%), F3 (2.81%), and F4 (37.3%). At 12.5 mg/kg bw, F5 suppressed P. berghei by 91.09%, surpassing chloroquine (87.79%), and restored altered hematological indices and CD4+ counts. Compounds identified in F5 included caffeate, linalool, terpinene-4-ol, quinovic acid, quercetin, prosopinine, catechin, and apigeninin. In conclusion, the fraction F5 of P. africana stem bark exhibited higher antimalarial activity than chloroquine and the identified compound might likely contribute to its activity.
Metrics
References
Adebayo JO, Krettl AU (2011). Potential antimalarials from Nigerian plants: a review. Journal of Ethnopharmacology 133(2):289-302. https://doi.org/10.1016/j.jep.2010.11.024
Afifi NA, Ibrahim MA, Galal MK (2018). Hepatoprotective influence of quercetin and ellagic acid on thioacetamide-induced hepatotoxicity in rats. Canadian Journal of Physiology and Pharmacology 96(6):624-629. https://doi.org/10.1139/cjpp-2017-0651
Akinosoglou KS, Solomou EE, Gogos CA (2012). Malaria: a hematological disease. Hematology 17(2):106-114. https://doi.org/10.1179/102453312X13221316477336
Amiri M, Nourian A, Khoshkam M, Ramazani A (2018). Apigenin inhibits the growth of the Plasmodium berghei and disrupts some metabolic pathways in mice. Phytotherapy Research 32(9):1795-1802. https://doi.org/10.1002/ptr.6113
Andrade-Cetto A, Heinrich M (2005). Mexican plants with hypoglycaemic effects are used in the treatment of diabetes. Journal of Ethnopharmacology 99(3):325-348. https://doi.org/10.1016/j.jep.2005.04.019
Asangha EE, Igile GO, Iwara IA, Ebong PE, Eseyin OA (2017). Hematological indices of Plasmodium berghei infected mice treated with ethanol extract and fractions of Nauclea latifolia roots. International Journal of Current Microbiology and Applied Sciences 6(12):2546-2556. https://doi.org/10.20546/ijcmas.2017.612.295
Aziz MA, Adnan M, Khan AH, Shahat AA, Al-Said MS, Ullah R (2018). Traditional uses of medicinal plants practiced by the indigenous communities at Mohmand Agency, FATA, Pakistan. Journal of Ethnobiology and Ethnomedicine 14:1-16. https://doi.org/10.1186/s13002-017-0204-5
Bagnarello-Madrigal V, Rodríguez-Chaves D, Alpizar-Cordero J, Calvo-Vargas A, Cordero-Villalobos M, Chinchilla-Carmona M, Valerio-Campos I, Sánchez-Porras R (2018). Antimalarial activity of an alkaloid mixture isolated from the tender leaves of the Nectandra membranacea (Laureaceae). Journal of Life Sciences 12:134-140. https://doi.org/10.17265/1934-7391/2018.03.003
Barbagallo I, Li Volti G, Raffaele M, Distefano A, Palmeri R, Parafati L, … Vanella L (2017). The effects of olive leaf extract from a Sicilian cultivar in an experimental model of hepatic steatosis. Rendiconti Lincei 28:643-650. https://doi.org/10.1007/s12210-017-0649-4
Bekono BD, Ntie-Kang F, Onguéné PA, Lifongo LL, Sippl W, Fester K, Owono LC (2020). The potential of anti-malarial compounds derived from African medicinal plants: a review of pharmacological evaluations from 2013 to 2019. Malaria Journal 19(1):1-35. https://doi.org/10.1186/s12936-020-03231-7
Bouyou Akotet MK, Koumba Lengongo JV, Ondounda M, Kendjo E, Mongo Delis A, Essomeyo Mebale M, … Okome Nkoumou M (2018). Burden of asymptomatic malaria, anemia and relationship with cotrimoxazole use and CD4 cell count among HIV1-infected adults living in Gabon, Central Africa. Pathogens and Global Health 112(2):63-71. https://doi.org/10.1080/20477724.2017.1401760
Espíndola KMM, Ferreira RG, Narvaez LEM, Silva Rosario ACR, Da Silva AHM, Silva AGB, … Monteiro MC (2019). Chemical and pharmacological aspects of caffeic acid and its activity in hepatocarcinoma. Frontiers in Oncology 541. https://doi.org/10.3389/fonc.2019.00541
Ettebong E, Ubulom P, Etuk A (2019). Antiplasmodial activity of methanol leaf extract of Citrus aurantifolia (Christm) Swingle. Journal of Herbmed Pharmacology 8(4):274-280. https://doi.org/10.15171/jhp.2019.40
Faleiro R, Karunarathne DS, Horne-Debets JM, Wykes M (2018). The contribution of co-signaling pathways to anti-malarial T cell immunity. Frontiers in Immunology 9:2926. https://doi.org/10.3389/fimmu.2018.02926
Francis U, Isaac Z, Yakubu A, Enosakhare A, Felix E (2014). Haematological parameters of malaria-infected patients in the University of Calabar Teaching Hospital, Calabar, Nigeria. Journal of Hematology & Thromboembolic Diseases. https://dx.doi.org/10.4172/2329-8790.1000171
Hu T, He XW, Jiang JG (2014). Functional analyses on antioxidant, anti-inflammatory, and antiproliferative effects of extracts and compounds from Ilex latifolia Thunb., a Chinese bitter tea. Journal of Agricultural and Food Chemistry 62(34):8608-8615. https://doi.org/10.1021/jf501670v
Igoli JO, Ogaji OG, Tor-Ayiin TA, Igoli NP (2005). Traditional medicine practice amongst the Igede people of Nigeria. Part II. African Journal of Traditional, Complementary and Alternative Medicines 2(2):134-152.
Jiang H, Wang J, Song L, Cao X, Yao X, Tang F, Yue Y (2016). GC× GC-TOFMS analysis of essential oils composition from leaves, twigs, and seeds of Cinnamomum camphora L. Presl and their insecticidal and repellent activities. Molecules 21(4):423. https://doi.org/10.3390/molecules21040423
Karama I, Compaoré M, Djandé A, Traoré O, Lagnika L, Kiendrebeogo M (2020). Antiplasmodial activities of flavonoids from leaves of Securidaca long pedunculate Fresen (Polygalaceae). American Journal of BioScience 8(1):1-5. https://doi.org/10.11648/j.ajbio.20200801.11
Kimbi HK, Sumbele IU, Nweboh M, Anchang-Kimbi JK, Lum E, Nana Y, Ndip LM, Njom H, Lehman LG (2013). Malaria and haematologic parameters of pupils at different altitudes along the slope of Mount Cameroon: a cross-sectional study. Malaria Journal 12(1):1-10. https://doi.org/10.1186/1475-2875-12-193
Kumar R, Loughland JR, Ng SS, Boyle MJ, Engwerda CR (2020). The regulation of CD4+ T cells during malaria. Immunological Reviews 293(1):70-87. https://doi.org/10.1111/imr.12804
Kumar V, Upadhyay N, Singh S, Singh J, Kaur P (2013). Thin-layer chromatography: comparative estimation of soil’s atrazine. Current World Environment 8(3):469. https://dx.doi.org/10.12944/CWE.8.3.17
Lubes G, Goodarzi M (2017). Analysis of volatile compounds by advanced analytical techniques and multivariate chemometrics. Chemical Reviews 117(9):6399-6422. https://doi.org/10.1021/acs.chemrev.6b00698
Mahajan BK (1997). Significance of difference in means. Methods in Biostatistics for Medical and Research Workers 6:130-155.
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 Complementary and Alternative Medicine 19(1):1-12. https://doi.org/10.1186/s12906-019-2567-8
Okaiyeto K, Okoh AI (2020). In vitro assessment of antiplasmodial and antitrypanosomal activities of chloroform, ethyl acetate and ethanol leaf extracts of Oedera genistifolia. Applied Sciences 10(19):6987. https://doi.org/10.3390/app10196987
Olakunle TP, Yusu GT, Busari T, Ogunkanmi LA, Lawal TR, Agboola JO (2019). In-vivo antimalaria activities of ethanolic extract of Morinda lucida in Plasmodium berghei infected mice. FUOYE Journal of Pure and Applied Sciences (FJPAS) 4(1):76-87.
Omarine Nlinwe N, Nange TB (2020). Assessment of hematological parameters in malaria, among adult patients attending the Bamenda Regional Hospital. Anemia 2020:1-8. https://doi.org/10.1155/2020/3814513
Peters DE, Ezendiokwere EO, Njoku UC, Wegwu MO (2017). Antimalarial activity of ethanolic leaf extract of Maesobotrya barteri and effects on some hematological and biochemical parameters of mice. Journal of Applied Life Sciences International 12(4):1-15. https://doi.org/10.9734/JABB/2017/32994
Ryley JF, Peters W (1970). The antimalarial activity of some quinolone esters. Annals of Tropical Medicine & Parasitology 64(2):209-222. https://doi.org/10.1080/00034983.1970.11686683
Shapira S, Pleban S, Kazanov D, Tirosh P, Arber N (2016). Terpinen-4-ol: A novel and promising therapeutic agent for human gastrointestinal cancers. PloS One 11(6):e0156540. https://doi.org/10.1371/journal.pone.0156540
van der Pluijm RW, Imwong M, Chau NH, Hoa NT, Thuy-Nhien NT, Thanh NV … Runjarern R (2019). Determinants of dihydroartemisinin-piperaquine treatment failure in Plasmodium falciparum malaria in Cambodia, Thailand, and Vietnam: a prospective clinical, pharmacological, and genetic study. The Lancet Infectious Diseases 19(9):952-961. https://dx.doi.org/10.1016/S1473-3099(19)30391-3
World Health Organization (2020). Report on antimalarial drug efficacy, resistance and response: 10 years of surveillance (2010-2019). World Health Organization.
Yan X, Qi M, Li P, Zhan Y, Shao H (2017). Apigenin in cancer therapy: Anti-cancer effects and mechanisms of action. Cell & Bioscience 7(1):1-16. https://doi.org/10.1186/s13578-017-0179-x
Yazici SO, Ozmen I, Yildirim B, Genc H, Ozeloglu B, Gulsun M, Elmas H, Ozcaka S (2020). Biochemical composition of Lathyrus l. seeds: antioxidant activities, phenolic profiles, β-odap and protein contents. Legume Research-An International Journal 43(5):723-727. https://doi.org/10.18805/LR-516
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2024 Fatimah A. ABUBAKAR, Hussain O.B. OLOYEDE, Musa O. SALAWU

This work is licensed under a Creative Commons Attribution 4.0 International License.
Papers published in Notulae Scientia Biologicae are Open-Access, distributed under the terms and conditions of the Creative Commons Attribution License.
© Articles by the authors; licensee SMTCT, Cluj-Napoca, Romania. The journal allows the author(s) to hold the copyright/to retain publishing rights without restriction.
License:
Open Access Journal - the journal offers free, immediate, and unrestricted access to peer-reviewed research and scholarly work, due SMTCT supports to increase the visibility, accessibility and reputation of the researchers, regardless of geography and their budgets. Users are allowed to read, download, copy, distribute, print, search, or link to the full texts of the articles, or use them for any other lawful purpose, without asking prior permission from the publisher or the author.