Antimalarial Effects of Areca catechu L.

  • Jiang, Jing-Hua (Department of Infection Biology, Zoonosis Research Center, Wonkwang University School of Medicine) ;
  • Jung, Suk-Yul (Department of Infection Biology, Zoonosis Research Center, Wonkwang University School of Medicine) ;
  • Kim, Youn-Chul (College of Pharmacy, Wonkwang University) ;
  • Shin, Sae-Ron (Department of Family Medicine, College of Medicine, Wonkwang University) ;
  • Yu, Seung-Taek (Department of Pediatrics, College of Medicine, Wonkwang University) ;
  • Park, Hyun (Department of Infection Biology, Zoonosis Research Center, Wonkwang University School of Medicine)
  • Published : 2009.04.25

Abstract

The emergence and spread of drug-resistant malaria parasites is a serious public health problem in the tropical world. Useful antimalarial drugs such as chloroquine have resistance in the world now. Moreover, other antimalarialdrugs such as mefloquine, halofantrine, atovaquone, proguanil, artemether and lumefantrine retain efficacy but have limitations, one of which is their high cost. New antimalarial drugs are clearly needed now. Cytotoxicity assay and susceptibility assay were performed for the selectivity of herb extracts in vitro. On the basis of high selectivity, 4-day suppressive test and survival test were progressed in Plasmodium berghei-infected mice. The selectivity of Areca catechu L. (ACL) and butanol extract of ACL (ACL-BuOH extract) were 3.4 and 3.0 in vitro, respectively. Moreover in vivo, 4-day suppressive test showed 39.1 % inhibition effect after treated with 150 mg/kg/day ACL-BuOH to P. berghei-infected mice. Survival test also showed 60% survival rate with ACL-BuOH-treated group while all other group mice died. In this study, ACL and ACL-BuOH were investigated for antimalarial activity in vitro and in vivo and they showed a potent antimalarial activity. In particular,ACL-BuOH could specifically lead higher survival rate of mice in vivo. Therefore ACL-BuOH would be a candidate of antimalarial drugs.

Keywords

References

  1. R. Tuteja. Malaria-the global disease. FEBS J. 274: 4669-4669, 2007 https://doi.org/10.1111/j.1742-4658.2007.05996.x
  2. A.F. Cowman and B.S. Crabb. Invasion of red blood cells by malaria parasites. Cell. 124: 755-766, 2006 https://doi.org/10.1016/j.cell.2006.02.006
  3. D.C. Deepak Gaur, M. Ghislaine and H.M. Louis. Parasite ligand-host interactions during invasion of erythrocytes by Plasmodium merozoites. Int. J. Parasitol. 34: 1413-1429, 2004 https://doi.org/10.1016/j.ijpara.2004.10.010
  4. R.G. Ridley. Medical need, scientific opportunity and the drive for antimalarial drugs. Nature. 415: 686-693, 2002 https://doi.org/10.1038/415686a
  5. J.R. Philip. Antimalarial chemotherapy: Mechanisms of action, resistance, and new directions in drug discovery, 2001
  6. J.A. Barltrop, T.C. Owen, A.H. Cory and J.G. Cory. 5-(3-carboxymethoxyphenyl)-2-(4,5-dimenthylthiazoly)-3-(4-sulfophenyl) tetrazolium, inner salt (MTS) and related analogs of 3-(4,5- dimethylthiazolyl)-2, 5-diphenyltetrazolium bromide (MTT) reducing to purple water soluble formazans as cell-viability indicators. Bioorg. Med. Chem. Lett. 1: 611-614, 1991 https://doi.org/10.1016/S0960-894X(01)81162-8
  7. A.A. Djimde, L. Kirkman, L. Kassambara, M. Diallo, C.V. Plowe, T.E. Wellems and O.K. Doumbo. In vitro cultivation of fields isolates of Plasmodium falciparum in Mali. Bull. Soc. Pathol. Exot. 100: 3-5, 2007 https://doi.org/10.3185/pathexo2883
  8. O. Bouchaud, S. Houze, Longuet, C., J.P. di Piazza, C. Ruggieri, Y. Secardin, J.P. Coulaud and J. Le Bras. Use of the parasight${\circledR}$-F Diagnostic test for imported malaria in a travel clinic. Am. J. Trop. Med. Hyg. 63: 76-79, 2000 https://doi.org/10.4269/ajtmh.2000.63.76
  9. M.T. Le, T.R. Bretschneider, C. Kuss and P.R. Preiser. A novel semi-automatic image processing approach to determine Plasmodium falciparumparasitemia in Giemsa-stained thin blood smears. BMC cell Biol. 28: 9-15, 2008
  10. W. Trager and J.B. Jensen. Human malaria parasites in continuous culture. Science. 193: 673-675, 1976 https://doi.org/10.1126/science.781840
  11. S. Hout and A. Chea. Screening of selected indigenous plants of Cambodia for antiplasmodial activity. J. Ethnopharmacol. 107: 12-18, 2006 https://doi.org/10.1016/j.jep.2006.01.028
  12. G.S. Dow, J. Oharaa, S.C. Newton, J.A. Reynoldson and R.C.A. Thompson. Plasmodium berghei: The Antimalarial Activity of Albendazole in Rats Is Mediated via Effects on the Hematopoietic System. Exp. Parasitol. 94: 259-263, 2000 https://doi.org/10.1006/expr.2000.4491
  13. W. Peters. The problem of drug resistance in malaria. Parasitology. 90: 705-715, 1985 https://doi.org/10.1017/S003118200005232X
  14. L.H. Carvalho and M.G.L. Brand$\tilde{a}$o. Antimalarial activity of crude extracts from brazilian plants in vivo in Plasmodium berghei infected mice and in vitro against Plasmodium falciparum in culture. Braz. J. Med. Biol. Res. 24: 1113-1123, 1991
  15. Y. Li and Y.L. Wu. How chinese scientists discovered qinghaosu (artemisinin) and developed its derivatives? What are the future perspectives? Med. Tro. (Mars) 58: 9-12, 1998
  16. J.F. Deng, J. Ger, W.J. Tsai, W.F. Kao and C.C. Yang. Acute toxicitiesof betel nut: rare but probably overlooked events. J. Toxicol. Clin. Toxicol. 39: 355-360, 2001 https://doi.org/10.1081/CLT-100105155
  17. B.J. Boucher and N. Mannan, Metabolic effects of the consumption of Areca catechu. Addiction Biol. 7: 103-110, 2002 https://doi.org/10.1080/13556210120091464
  18. A.K. Fajimi and A.A. Taiwo. Herbal remedies in animal parasitic diseases in Nigeria: a review. African J. Biotech. 4: 303-307, 2004
  19. K.K. Lee and J.D. Choi. The effects of Areca Catechu L extract on anti-aging. Int. J. cosmet. Sci. 21: 285-295, 1999 https://doi.org/10.1046/j.1467-2494.1999.196563.x
  20. S.M. Jeon, H.S. Kim, T.G. Lee, S.H. Ryu, P.G. Suh, S.J. Byun, Y.B. Park and M.S. Choi. Lower absorption of cholesteryl oleate in rats supplemented with Areca catechu L. extract. Ann. Nutr. Metab. 44: 170-176, 2000 https://doi.org/10.1159/000012841
  21. S.J. Byun, H.S. Kim, S.M. Jeon, Y.B. Park and M.S. Choi. Supplementation of Areca catechu L. extract alters triglyceride absorption and cholesterol metabolism in rats. Ann. Nutr. Metab. 45: 279-284, 2001 https://doi.org/10.1159/000046739
  22. S.I. Hay, D.J. Rogers, J.F. Toomer and R.W. Snow. Annual Plasmodium falciparum entomological inoculation rates (EIR) across Africa: literature survey, Internet access and review. Trans. R. Soc. Trop. Med. Hyg. 94: 113-127, 2000 https://doi.org/10.1016/S0035-9203(00)90246-3
  23. C. Lengeler, T.A. Smith and J. Armstrong Schellenberg. Focus on the effect of bednets on malaria morbidity and mortality. Parasitol. Today 13: 123-124, 1997. https://doi.org/10.1016/S0169-4758(97)84870-3
  24. G.T. Webster, L. Tilley, S. Deed, D. McNaughton, B.R. Wood. Resonance Raman spectroscopy can detect structural changes in haemozoin (malaria pigment) following incubation with chloroquine in infected erythrocytes. FEBS Lett. 582: 1087-1092, 2008 https://doi.org/10.1016/j.febslet.2008.02.062