Prophylactic antimalarial effects of Cymbopogon citratus (DC.) Stapf (Poaceae) in a mouse model of Plasmodium berghei ANKA infection: normalisation of haematological and serum biochemical status

Authors

  • Raymond Bess Bila Department of Zoology and Animal Physiology, Faculty of Science, University of Buea, Cameroon
  • Germain Sotoing Taiwe Department of Zoology and Animal Physiology, Faculty of Science, University of Buea, Cameroon
  • David Denis Feugaing Sofeu Department of Biochemistry and Molecular Biology, Faculty of Science, University of Buea, Cameroon
  • Orelien Sylvain Mtopi Bopda Department of Zoology and Animal Physiology, Faculty of Science, University of Buea, Cameroon
  • Hart Mann Alain Youbi Mambou Department of Zoology and Animal Physiology, Faculty of Science, University of Buea, Cameroon
  • Seraphin Nji Ombel Musa Department of Zoology and Animal Physiology, Faculty of Science, University of Buea, Cameroon
  • Liliane Laure Toukam Department of Microbiology and Parasitology, Faculty of Science, University of Buea, Buea, Cameroon
  • Helen Kuokuo Kimbi Department of Biomedical Sciences, University of Bamenda, Cameroon

DOI:

https://doi.org/10.30574/gscbps.2021.15.1.0084

Keywords:

Cymbopogon citratus, malaria prophylaxis, haematological and biochemical, mouse model

Abstract

Ethnopharmacological relevance: Cymbopogon citratus (DC.) Stapf (Poaceae) is a medicinal plant known for its antimalarial, antipyretic and antifatigue activities in Cameroonian folk medicine.

Aim of the study: The aim of this work was to evaluate the prophylactic antimalarial effects of the decoction prepared from the leaves of Cymbopogon citratus on Plasmodium berghei ANKA infection in mice and investigate its action on haematological and serum biochemical status.

Materials and methods: Swiss mice were treated with Cymbopogon citratus leaf decoction (25, 50, 100 and 200 mg/kg) and later inoculated with Plasmodium berghei ANKA. The prophylactic antimalarial activity of the decoction was evaluated by determining the parasitaemia, percentage chemosuppression, body weight, body temperature, food and water intake in pretreated parasitised mice. The possible ameliorative effects of the decoction on malaria associated haematological and serum biochemical changes were also assessed.

Results: The decoction exhibited a prophylactic activity of 85.32% and its chemotherapeutic effects ranged from 56.88 – 85.32% with maximum effect observed at the highest experimental dose. It significantly inhibited parasitaemia (P < 0.001) compared to the negative control group.   Interestingly, treatment of parasitised mice with the decoction significantly restored the malaria modified haematological and biochemical status compared with distilled water-treated parasitised mice.

Conclusion: The results of this prophylactic assay indicated that Cymbopogon citratus decoction has antimalarial effects and normalised haematological and serum biochemical aberrations generated by malaria. Hence, Cymbopogon citratus represents a promising source of new antimalarial agents.

Metrics

Metrics Loading ...

References

World Health Organization. World malaria report 2015: World Health Organization; 2016.

Alonso P, Noor AM. The global fight against malaria is at crossroads. The Lancet. 2017; 390(10112):2532-4.

Coelho CH, Rappuoli R, Hotez PJ, Duffy PE. Transmission-blocking vaccines for malaria: time to talk about vaccine introduction. Trends in parasitology. 2019; 35(7):483-6.

Organization WH. Global report on insecticide resistance in malaria vectors: 2010–2016. 2018.

Cheeseman IH, McDew-White M, Phyo AP, Sriprawat K, Nosten F, Anderson TJ. Pooled sequencing and rare variant association tests for identifying the determinants of emerging drug resistance in malaria parasites. Molecular biology and evolution. 2015; 32(4):1080-90.

Rodak BF, Keohane EM, Fritsma GA. Hematology-E-Book: Clinical Principles and Applications: Elsevier Health Sciences; 2013.

Kausar MW, Moeed K, Asif N, Rizwi F, Raza S. Correlation of bilirubin with liver enzymes in patients of falciparum malaria. International Journal of Pathology. 2010; 8(2):63-7.

Adebayo J, Krettli A. Potential antimalarials from Nigerian plants: a review. Journal of ethnopharmacology. 2011; 133(2):289-302.

Avoseh O, Oyedeji O, Rungqu P, Nkeh-Chungag B, Oyedeji A. Cymbopogon species; ethnopharmacology, phytochemistry and the pharmacological importance. Molecules. 2015; 20(5):7438-53.

Santoro G, Cardoso M, Guimarães L, Freire J, Soares M. Anti-proliferative effect of the essential oil of Cymbopogon citratus (DC) Stapf (lemongrass) on intracellular amastigotes, bloodstream trypomastigotes and culture epimastigotes of Trypanosoma cruzi (Protozoa: Kinetoplastida). Parasitology. 2007; 134(11):1649-56.

Ginsburg H, Deharo E. A call for using natural compounds in the development of new antimalarial treatments–an introduction. Malaria journal. 2011; 10(1):1-7.

Ntonga PA, Baldovini N, Mouray E, Mambu L, Belong P, Grellier P. Activity of Ocimum basilicum, Ocimum canum, and Cymbopogon citratus essential oils against Plasmodium falciparum and mature-stage larvae of Anopheles funestus ss. Parasite. 2014; 21.

Chukwuocha UM, Fernández-Rivera O, Legorreta-Herrera M. Exploring the antimalarial potential of whole Cymbopogon citratus plant therapy. Journal of ethnopharmacology. 2016; 193:517-23.

Taiwe GS, Kouamou ALN, Ambassa ARM, Menanga JR, Tchoya TB, Dzeufiet PDD. Evidence for the involvement of the GABA-ergic pathway in the anticonvulsant activity of the roots bark aqueous extract of Anthocleista djalonensis A. Chev. (Loganiaceae). Journal of basic and clinical physiology and pharmacology. 2017; 28(5):425-35.

Bantie L, Assefa S, Teklehaimanot T, Engidawork E. In vivo antimalarial activity of the crude leaf extract and solvent fractions of Croton macrostachyus Hocsht. (Euphorbiaceae) against Plasmodium berghei in mice. BMC complementary and alternative medicine. 2014; 14(1):1-10.

Peters W. Drug resistance in Plasmodium berghei. I. Chloroquine resistance. Experimental parasitology. 1965; 17(1):80-9.

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. Malaria journal. 2014; 13(1):1-11.

Balcombe JP, Barnard ND, Sandusky C. Laboratory routines cause animal stress. Journal of the American Association for Laboratory Animal Science. 2004; 43(6):42-51.

Nghonjuyi NW, Tiambo CK, Taïwe GS, Toukala JP, Lisita F, Juliano RS, et al. Acute and sub-chronic toxicity studies of three plants used in Cameroonian ethnoveterinary medicine: Aloe vera (L.) Burm. f. (Xanthorrhoeaceae) leaves, Carica papaya L. (Caricaceae) seeds or leaves, and Mimosa pudica L.(Fabaceae) leaves in Kabir chicks. Journal of ethnopharmacology. 2016; 178:40-9.

Dada E, Adebayo R. Antiplasmodial Activity of Ethanolic Leaf Extract of Cymbopogon citratus (DC) Stapf in Swiss Albino Mice Infected with Plasmodium berghei NK 65. South Asian Journal of Research in Microbiology. 2020: 27-38.

Golenser J, Waknine JH, Krugliak M, Hunt NH, Grau GE. Current perspectives on the mechanism of action of artemisinins. International journal for parasitology. 2006; 36(14):1427-41.

Hansen DS. Inflammatory responses associated with the induction of cerebral malaria: lessons from experimental murine models. PLoS Pathog. 2012; 8(12):e1003045.

Petersen I, Eastman R, Lanzer M. Drug-resistant malaria: molecular mechanisms and implications for public health. FEBS letters. 2011; 585(11):1551-62.

Hill DR, Baird JK, Parise ME, Lewis LS, Ryan ET, Magill AJ. Primaquine: report from CDC expert meeting on malaria chemoprophylaxis I. The American journal of tropical medicine and hygiene. 2006; 75(3):402-15.

Dow GS, Magill AJ, Ohrt C. Clinical development of new prophylactic antimalarial drugs after the 5th Amendment to the Declaration of Helsinki. Therapeutics and clinical risk management. 2008; 4(4):803.

Imaculada Muniz-Junqueira M. Immunomodulatory therapy associated to anti-parasite drugs as a way to prevent severe forms of malaria. Current Clinical Pharmacology. 2007; 2(1):59-73.

Masihi KN. Fighting infection using immunomodulatory agents. Expert opinion on biological therapy. 2001; 1(4):641-53.

Chinchilla M, Guerrero OM, Abarca G, Barrios M, Castro O. An in vivo model to study the anti-malaric capacity of plant extracts. Revista de Biología Tropical. 1998; 46(1):35-9.

Chaniad P, Techarang T, Phuwajaroanpong A, Punsawad C. Antimalarial activity and toxicological assessment of Betula alnoides extract against plasmodium berghei infections in mice. Evidence-Based Complementary and Alternative Medicine. 2019; 2019.

Hintsa G, Sibhat GG, Karim A. Evaluation of antimalarial activity of the leaf latex and TLC isolates from Aloe megalacantha Baker in Plasmodium berghei infected mice. Evidence-Based Complementary and Alternative Medicine. 2019; 2019.

Ugwuene M. Effect of dietary palm kernel meal for maize on the haematological and serum chemistry of broiler turkey. Nigerian Journal of Animal Science. 2011; 13:93-103.

Isaac L, Abah G, Akpan B, Ekaette I, editors. Haematological properties of different breeds and sexes of rabbits. Proceedings of the 18th Annual Conference of Animal Science Association of Nigeria; 2013.

Ugwu OP, Nwodo OF, Joshua PE, Odo CE, Bawa A, Ossai E, et al. Anti-malaria and hematological analyses of ethanol leaf extract of Moringa oleifera on malaria infected mice. International Journal of Pharmacy and Biological Science. 2013; 3(1):360-71.

Briggs C, Bain BJ. Basic haematological techniques. Dacie and Lewis practical haematology: Elsevier; 2012. p. 23-56.

Erhart LM, Yingyuen K, Chuanak N, Buathong N, Laoboonchai A, Miller RS, et al. Hematologic and clinical indices of malaria in a semi-immune population of western Thailand. The American journal of tropical medicine and hygiene. 2004; 70(1):8-14.

Ifeanyichukwu M, Esan A. Evaluation of blood cells and platelets in Plasmodium falciparum malaria infected individuals. International Journal of Haematological Disorders. 2014; 1(1):49-54.

Koffuor G, Dadzeasah P, Sam G. Haematopoietic effect of an ethanolic leaf extract of Ipomoea in-volucrata P. Beauv in phlebotomized New Zealand White Rabbits. Journal of medical and biomedical sciences. 2012; 1(2).

Oyedapo O, Famurewa AJ. Antiprotease and membrane stabilizing activities of extracts of Fagara zanthoxyloides, Olax subscorpioides and Tetrapleura tetraptera. International journal of Pharmacognosy. 1995; 33(1):65-9.

Trampuz A, Jereb M, Muzlovic I, Prabhu RM. Clinical review: Severe malaria. Critical care. 2003; 7(4):1-9.

Orhue N, Nwanze E, Akafor A. Serum total protein, albumin and globulin levels in Trypanosoma brucei-infected rabbits: Effect of orally administered Scoparia dulcis. African Journal of Biotechnology. 2005; 4(10).

George B, Osioma E, Okpoghono J, Aina O. Changes in liver and serum transaminases and alkaline phosphatase enzyme activities in Plasmodium berghei infected mice treated with aqueous extract of Aframomum sceptrum. African Journal of Biochemistry Research. 2011; 5(9):277-81.

Guthrow CE, Morris MA, Day JF, Thorpe SR, Baynes JW. Enhanced nonenzymatic glucosylation of human serum albumin in diabetes mellitus. Proceedings of the National Academy of Sciences. 1979; 76(9):4258-61.

Downloads

Published

2021-04-30

How to Cite

Raymond Bess Bila, Germain Sotoing Taiwe, David Denis Feugaing Sofeu, Orelien Sylvain Mtopi Bopda, Hart Mann Alain Youbi Mambou, Seraphin Nji Ombel Musa, Liliane Laure Toukam, & Helen Kuokuo Kimbi. (2021). Prophylactic antimalarial effects of Cymbopogon citratus (DC.) Stapf (Poaceae) in a mouse model of Plasmodium berghei ANKA infection: normalisation of haematological and serum biochemical status. GSC Biological and Pharmaceutical Sciences, 15(1), 05–017. https://doi.org/10.30574/gscbps.2021.15.1.0084

Issue

Section

Original Article