Skip to main content

Advertisement

Log in

Haemin enhances the in vivo efficacy of artemether against juvenile and adult Schistosoma mansoni in mice

  • Original Paper
  • Published:
Parasitology Research Aims and scope Submit manuscript

An Erratum to this article was published on 18 April 2013

Abstract

Among the potential alternatives to praziquantel, interestingly, the antimalarial artemether (Art) also exhibits antischistosomal properties. Previous in vitro studies suggested that Art interacts with haemin and together produce a lethal agent against schistosomes. This study investigates the in vivo effect of Art plus haemin on juvenile and adult Schistosoma mansoni worms and on their antioxidant enzymes. Infected mice were allocated into two batches each in four groups (I-IV): (I) untreated control; (II) injected with haemin (ip, 100 mg/kg/day) on days 26, 27, and 28 post-infection (PI) for juvenile stage and on days 47, 48, and 49 PI for adult stage; (III) treated with a single oral dose of Art (300 mg/kg) either after 28 or 49 days PI, respectively; and (IV) received both haemin, as group (II) and Art as group (III). Half of mice for each batch were killed 72 h; meanwhile, the remaining half was killed 3 weeks after Art administration. Parasitological criteria of cure and worms’ antioxidant enzymes were assessed. Glutathione S-transferase (GST), glutathione peroxidase (GPx), glutathione reductase (GR), and superoxide dismutase (SOD) activities were lower in juvenile worms than adult ones and in females than males. Haemin plus Art at the juvenile and adult stages produced significant inhibition in worms’ GST, GPx, and SOD activities 72 h after Art treatment, compared with Art-treated group, with enhanced killing of females (96.98 and 91.47 % versus 87.04 and 72.97 %, respectively) and total worms (91 and 83.39 % versus 75 and 59.01 %, respectively) 3 weeks posttreatment. In conclusion, Art plus haemin has a higher harmful effect on juvenile and adult schistosomes and antioxidant capacity than Art alone. This gives new insights into the importance of haemin in the antischistosomal properties of artemether.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Abdul-Ghani R, Loutfy N, Sheta M, Hassan A (2011) Artemether shows promising female schistosomicidal and ovicidal effects on the Egyptian strain of Schistosoma mansoni after maturity of infection. Parasitol Res 108:1199–1205

    Article  PubMed  Google Scholar 

  • Bethony JM (2008) Can schistosomiasis really be consigned to history without a vaccine? Vaccine 26:3373–3376

    Article  PubMed  Google Scholar 

  • Brophy PM, Barrett J (1990) Glutathione transferase in helminths. Parasitology 100:345–349

    Article  PubMed  CAS  Google Scholar 

  • Butler AR, Gilbert BC, Hulme P, Irvine LR, Renton L, Whitwood AC (1998) EPR evidence for the involvement of free radicals in the iron-catalysed decomposition of qinghaosu (artemisinin) and some derivatives; antimalarial action of some polycyclic endoperoxides. Free Radic Res 28:471–476

    Article  PubMed  CAS  Google Scholar 

  • Doenhoff MJ, Cioli D, Utzinger J (2008) Praziquantel: mechanisms of action, resistance and new derivatives for schistosomiasis. Curr Opin Infect Dis 21:659–667

    Article  PubMed  CAS  Google Scholar 

  • Duvall RH, De Witt WB (1967) An improved perfusion technique for recovering adult schistosomes from laboratory animals. AmJTrop Med Hyg 16:483–486

    CAS  Google Scholar 

  • El-Lakkany NM, Seif el-Din SH, Badawy AA, Ebeid FA (2004) Effect of artemether alone and in combination with grapefruit juice on hepatic drug metabolizing enzymes and biochemical aspects in experimental Schistosoma mansoni. Int J Parasitol 34:1405–1412

    Article  PubMed  CAS  Google Scholar 

  • Fibach E, Kollia P, Schechter AN, Noguchi CT, Rodgers GP (1995) Hemin-induced acceleration of hemoglobin production in immature cultured erythroid cells: preferential enhancement of fetal hemoglobin. Blood 85:2967–2974

    PubMed  CAS  Google Scholar 

  • Golenser J, Waknine JH, Krugliak M, Hunt NH, Grau GE (2006) Current perspectives on the mechanism of action of artemisinins. Inter J Parasitol 36:1427–1441

    Article  CAS  Google Scholar 

  • Habig WH, Pabst MJ, Jakoby WB (1974) Glutathione S-transferase: the first enzymatic step in mercapturic acid formation. J Biol Chem 249:7130–7139

    PubMed  CAS  Google Scholar 

  • Haynes RK (2001) Artemisinin and derivatives: the future for malaria treatment? Curr Opin Infect Dis 14:719–726

    Article  PubMed  CAS  Google Scholar 

  • Holy JM, O’Leary KA, Oaks JA, Tracy JW (1989) Immunocytochemical localization of the major glutathione S-transferases in adult Schistosoma mansoni. J Parasitol 75:181–190

    Article  PubMed  CAS  Google Scholar 

  • Hong YL, Yang YZ, Meshnick SR (1994) The interaction of artemisinin with malarial hemozin. Mol Biochem Parasitol 63:121–128

    Article  PubMed  CAS  Google Scholar 

  • Hong Z, LoVerde PT, Hammarskjold ML, Rekosh D (1992) Schistosoma mansoni: cloning of a complementary DNA encoding a cytosolic Cu/Zn superoxide dismutase and high yield expression of the enzymatically active gene product in Escherichia coli. Exp Parasitol 75:308–322

    Article  PubMed  CAS  Google Scholar 

  • James ER (1994) Superoxide dismutase. Parasitol Today 10:481–484

    Article  PubMed  CAS  Google Scholar 

  • Kamel IA, Cheever AW, Elwi AM, Mosimann JE, Danner R (1977) Schistosoma mansoni and S. haematobium infections in Egypt. I. Evaluation of techniques for recovery of worms and eggs at necropsy. Am J Trop Med Hyg 26:696–701

    PubMed  CAS  Google Scholar 

  • Karbwang J, Na-Bangchang K, Thanavibul A, Molunto P (1998) Plasma concentrations of artemether and its major plasma metabolite, dihydroartemisinin, following a 5-day regimen of oral artemether, in patients with uncomplicated falciparum malaria. Ann Trop Med Parasitol 92:31–36

    Article  PubMed  CAS  Google Scholar 

  • Keiser J, Utzinger J (2007) Artemisinins and synthetic trioxolanes in the treatment of helminth infections. Curr Opin Infect Dis 20:605–612

    Article  PubMed  CAS  Google Scholar 

  • Kloetzel K, Lewert RM (1996) Pigment formation in Schistosoma mansoni infections in the white mouse. Am J Trop Med Hyg 15:28–31

    Google Scholar 

  • Lawrence JD (1973) The ingestion of red blood cells by Schistosoma mansoni. J Parasitol 59:60–63

    Article  PubMed  CAS  Google Scholar 

  • Liang YS, John BI, Boyd DA (1987) Laboratory cultivation of schistosome vector snails and maintenance of schistosome life cycles. Proceeding of the 1st Sino-American Symposium1 34–48

  • Liu R, Dong HF, Jiang MS (2012) Artemisinin: the gifts from traditional Chinese medicine not only for malaria control but also for schistosomiasis control. Parasitol Res 110:2071–2074

    Article  PubMed  Google Scholar 

  • LoVerde PT (1998) Do antioxidants play a role in schistosome host–parasite interactions? Parasitol Today 14:109–113

    Article  Google Scholar 

  • LoVerde PT, Carvalho-Queiroz C, Cook R (2004) Vaccination with antioxidant enzymes confers protective immunity against challenge infection with Schistosoma mansoni. Mem Inst Oswaldo Cruz Rio de Janeiro 99:37–43

    Article  CAS  Google Scholar 

  • Mei H, LoVerde PT (1997) Schistosoma mansoni: the developmental regulation and immunolocalization of antioxidant enzymes. Exp Parasitol 86:69–78

    Article  PubMed  CAS  Google Scholar 

  • Meshnick SR (2002) Artemisinin: mechanisms of action, resistance and toxicity. Int J Parasitol 32:1655–1660

    Article  PubMed  CAS  Google Scholar 

  • Mkoji GM, Smith JM, Prichard RK (1988) Antioxidant systems in Schistosoma mansoni: correlation between susceptibility to oxidant killing and the levels of scavengers of hydrogen peroxide and oxygen free radicals. Int J Parasitol 18:661–666

    Article  PubMed  CAS  Google Scholar 

  • Nare B, Smith JM, Prichard RK (1990) Schistosoma mansoni: levels of antioxidants and resistance to oxidants increase during development. Exp Parasitol 70:389–397

    Article  PubMed  CAS  Google Scholar 

  • Ndisang JF, Lane N, Jadhav A (2008) Crosstalk between the heme oxygenase system, aldosterone, and phospholipase C in hypertension. J Hypertens 26:1188–1199

    Article  PubMed  CAS  Google Scholar 

  • O’Leary KA, Tracy JW (1991) Schistosoma mansoni: glutathione S transferase-catalyzed detoxication of dichlorvos. Exp Parasitol 72:355–361

    Article  PubMed  Google Scholar 

  • Paglia DE, Valentine WN (1967) Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase. J Lab Clin Med 70:158–169

    PubMed  CAS  Google Scholar 

  • Pellegrino J, Oliveira CA, Faria J, Cunha AS (1962) New approach to the screening of drugs in experimental schistosomiasis mansoni in mice. Am J Trop Med Hyg 11:201–215

    PubMed  CAS  Google Scholar 

  • Porchet E, McNair A, Caron A, Kusnierz JP, Zemzoumi K, Capron A (1994) Tissue expression of the Schistosoma mansoni 28 kDa glutathione S-transferase. Parasitology 109:565–572

    Article  PubMed  CAS  Google Scholar 

  • Posner GH, Meshnick SR (2001) Radical mechanism of action of the artemisinin-type compounds. Trends Parasitol 17:266–267

    Article  PubMed  CAS  Google Scholar 

  • Scott JC, McManus DP (2000) Molecular cloning and enzymatic expression of the 28-kDa glutathione S-transferase of Schistosoma japonicum: evidence for sequence variation but lack of consistent vaccine efficacy in the murine host. Parasitol Int 49:289–300

    Article  PubMed  CAS  Google Scholar 

  • Steinmann P, Keiser J, Bos R, Tanner M, Utzinger J (2006) Schistosomiasis and water resources development: systematic review, meta-analysis, and estimates of people at risk. Lancet Infect Dis 6:411

    Article  PubMed  Google Scholar 

  • Utzinger J, Keiser J (2004) Schistosomiasis and soil-transmitted helminthiasis: common drugs for treatment and control. Expert Opin Pharmacother 5:263–285

    Article  PubMed  CAS  Google Scholar 

  • Utzinger J, Chollet J, You JQ, Mei JY, Tanner M, Xiao SH (2001) Effect of combined treatment with praziquantel and artemether on Schistosoma japonicum and Schistosoma mansoni in experimentally infected animals. Acta Trop 80:9–18

    Article  PubMed  CAS  Google Scholar 

  • Utzinger J, Chollet J, Zuwu T, Xiao SH, Tanner M (2002) Comparative study of the effects of artemether and artesunate on juvenile and adult Schistosoma mansoni in experimentally infected mice. Trans R Soc Trop Med Hyg 96:318–323

    Article  PubMed  CAS  Google Scholar 

  • Utzinger J, Xiao SH, Tanner M, Keiser J (2007) Artemisinins for schistosomiasis and beyond. Curr Opin Investig Drugs 8:105–116

    PubMed  CAS  Google Scholar 

  • Van Kampen E, Zulstra WG (1961) Standardization of hemoglobinometry. II. The hemiglobincyanide method. Clin Chim Acta 6:538–544

    Article  PubMed  Google Scholar 

  • Wang W, Wang L, Liang YS (2012) Susceptibility or resistance of praziquantel in human schistosomiasis: a review. Parasitol Res 111:1871–1877

    Article  PubMed  Google Scholar 

  • Winterbourn CC, Hawkins RE, Brian M, Carrell RW (1975) The estimation of red cell superoxide dismutase activity. J Lab Clin Med 85:337–342

    PubMed  CAS  Google Scholar 

  • Xiao SH, Catto BA (1989) In vitro and in vivo studies of the effect of artemether on Schistosoma mansoni. Antimicrob Agents Chemother 33:1557–1562

    Article  PubMed  CAS  Google Scholar 

  • Xiao SH, You JQ, Yang YQ, Wang CZ (1995) Experimental studies on early treatment of schistosomal infection with artemether. Southeast Asian J Trop Med Public Health 26:306–318

    PubMed  CAS  Google Scholar 

  • Xiao SH, You JQ, Mei JY, Guo HF, Jiao PY, Sun HL, Yao MY, Feng Z (1997) Effect of artemether on glucose uptake and glycogen content in Schistosoma japonicum. Acta Pharmacol Sin 18:363–367

    CAS  Google Scholar 

  • Xiao SH, You JQ, Mei JY, Jiao PY, Guo HF, Feng Z (1998) Preventive effect of artemether in rabbits infected with Schistosoma japonicum cercariae. Acta Pharmacol Sin 19:63–66

    CAS  Google Scholar 

  • Xiao SH, You JQ, Guo HF, Mei JY, Jiao PY, Yao MY, Zhuang ZN, Feng Z (1999) Effect of artemether on phosphorylase, lactate dehydrogenase, adenosine triphosphate, and glucosephosphate dehydrogenase of Schistosoma japonicum harbored in mice. Acta Pharmacol Sin 20:750–754

    CAS  Google Scholar 

  • Xiao SH, Chollet J, Weiss NA, Bergquist RN, Tanner M (2000a) Preventive effect of artemether in experimental animals infected with Schistosoma mansoni. Parasitol Int 49:19–24

    Article  Google Scholar 

  • Xiao SH, Utzinger J, Chollet J, Endriss Y, N’Goran EK, Tanner M (2000b) Effect of artemether against Schistosoma haematobium in experimentally infected hamsters. Int J Parasitol 30:1001–1006

    Article  PubMed  CAS  Google Scholar 

  • Xiao SH, Chollet J, Utzinger J, Matile H, Mei JY, Tanner M (2001) Artemether administered together with haemin damages schistosomes in vitro. Trans R Soc Trop Med Hyg 95:67–71

    Article  PubMed  CAS  Google Scholar 

  • Xiao SH, Tanner M, N’Goran EK, Utzinger J, Chollet J, Bergquist R, Chen M, Zheng J (2002a) Recent investigations of artemether, a novel agent for the prevention of Schistosomiasis japonica, mansoni and haematobia. Acta Trop 82:175–181

    Article  PubMed  CAS  Google Scholar 

  • Xiao SH, You JQ, Gao HF, Mei JY, Jiao PY, Chollet J, Tanner M, Utzinger J (2002b) Schistosoma japonicum: effect of artemether on glutathione S-transferase and superoxide dismutase. Exp Parasitol 102:38–45

    Article  PubMed  CAS  Google Scholar 

  • Xiao SH, Wu YL, Tanner M, Wu WM, Utzinger J, Mei JY, Scorneaux B, Chollet J, Zhai Z (2003) Schistosoma japonicum: in vitro effects of artemether combined with haemin depend on cultivation media and appraisal of artemether products appearing in the media. Parasitol Res 89:459–466

    PubMed  Google Scholar 

  • Yang YQ, Xiao SH, Tanner M, Utzinger J, Chollet J, Wu JD, Guo J (2001) Histopathological changes in juvenile Schistosoma haematobium harboured in hamsters treated with artemether. Acta Trop 79:135–141

    Article  PubMed  CAS  Google Scholar 

  • Yang YZ, Little B, Meshnick SR (1994) Alkylation of proteins by artemisinin. Effects of heme, pH, and drug structure. Biochem Pharmacol 48:569–573

    Article  PubMed  CAS  Google Scholar 

  • Zanetti G (1979) Rabbit liver glutathione reductase: purification and properties. Arch Biochem Biophys 198:241–246

    Article  PubMed  CAS  Google Scholar 

  • Zussman RA, Bauman PM, Petruska JC (1970) The role of hemoglobin in the nutrition of Schistosoma mansoni. J Parasitol 56:75–79

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgments

This work was supported by the internal research project 82/A for basic and applied research, a grant from Theodor Bilharz Research Institute.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Naglaa Mohamed El-Lakkany.

Rights and permissions

Reprints and permissions

About this article

Cite this article

El-Lakkany, N.M., Seif el-Din, S.H. Haemin enhances the in vivo efficacy of artemether against juvenile and adult Schistosoma mansoni in mice. Parasitol Res 112, 2005–2015 (2013). https://doi.org/10.1007/s00436-013-3358-7

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00436-013-3358-7

Keywords

Navigation