Literature DB >> 22006193

Effect of the in vivo activity of dihydroartemisinin against Schistosoma mansoni infection in mice.

Hong-jun Li1, Wei Wang, Guo-li Qu, You-zi Li, Yong-hui Tao, Yun-tian Xing, Xiao-ting Wang, Yang Dai, Jian-ying Wei, Jian-rong Dai, Gerald C Coles, You-sheng Liang.   

Abstract

Dihydroartemisinin, formerly known as an antimalarial drug, is the main metabolite of the mother compound artemisinins, as well as of artemether and artesunate. It has been shown that the drug exhibits antischistosomal efficacy against Schistosoma japonicum. The purpose of the current study was to assess the in vivo effect of dihydroartemisinin against Schistosoma mansoni infection in mice. Drugs at a single oral dose of 300 mg/kg were given to mice to assess the efficacy against different developmental stages of the parasite; juvenile and adult S. mansoni were treated with single doses of dihydroarteminisin with different regimens (at 200, 300, 400 or 600 mg/kg) in the stage of drug sensitivity, and the dose-response relationship was assessed; and the effect of multiple doses (at 200, 300 or 400 mg/kg) on juvenile and adult S. mansoni was also observed. The results showed that a single oral dose (300 mg/kg) of dihydroartemisinin reduced total worm burdens by 13.8-82.1% and female worm burdens by 13-82.8%, and the greatest reductions were seen when treatment was given on day 21 post-infection, with total and female worm burden reductions of 82.1% and 82.8%. Administration of a single oral dose of dihydroartemisinin on day 21 post-infection with different drug dosage (at 200, 300, 400 or 600 mg/kg) reduced total worm burdens by 70.3-87.3% and female worm burdens by 73.5-92.4%, depending on dosage. Similar treatments given on day 49 post-infection reduced total worm burdens by 48.7-68.73% and female worm burdens by 63.25-94.6%. There was obvious dose-response relationship of dihydroartemisinin against the schistosomula and adult worms of S. mansoni observed. Administration with dihydroartemisinin at oral doses of 200, 300 and 400 mg/kg, given once on each of days 20-22 post-infection of three successive days, reduced total worm burdens by 88.5-90.1% and female worm burdens by 89.2-92.1%, depending on dosage. Similar treatments given once on each of days 48-50 post-infection reduced total worm burdens by 60-70.3% and female worm burdens by 77.5-94.9%. It is concluded that dihydroartemisinin exhibits in vivo activity against various developmental stages of S. mansoni, particularly the 21-day schistosomula, and there is obvious dose-response relationship of dihydroartemisinin against the schistosomula and adult worms of S. mansoni observed.

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Year:  2011        PMID: 22006193     DOI: 10.1007/s00436-011-2692-x

Source DB:  PubMed          Journal:  Parasitol Res        ISSN: 0932-0113            Impact factor:   2.289


  41 in total

1.  Preventive effect of artemether in experimental animals infected with Schistosoma mansoni.

Authors:  X Shuhua; J Chollet; N A Weiss; R N Bergquist; M Tanner
Journal:  Parasitol Int       Date:  2000-03       Impact factor: 2.230

2.  Effect of artemether administered alone or in combination with praziquantel to mice infected with Plasmodium berghei or Schistosoma mansoni or both.

Authors:  Xiao Shu-Hua; Jürg Utzinger; Jacques Chollet; Marcel Tanner
Journal:  Int J Parasitol       Date:  2006-04-25       Impact factor: 3.981

3.  Efficacy and side effects of praziquantel in an epidemic focus of Schistosoma mansoni.

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4.  Synthesis and properties of Praziquantel, a novel broad spectrum anthelmintic with excellent activity against Schistosomes and Cestodes.

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Journal:  Experientia       Date:  1977-08-15

5.  Oral artemether for prevention of Schistosoma mansoni infection: randomised controlled trial.

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Journal:  Lancet       Date:  2000-04-15       Impact factor: 79.321

6.  The infection of laboratory hosts with cercariae of Schistosoma mansoni and the recovery of the adult worms.

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Journal:  Parasitology       Date:  1965-11       Impact factor: 3.234

7.  Susceptibility of Schistosoma japonicum to different developmental stages to praziquantel.

Authors:  S H Xiao; W J Yue; Y Q Yang; J Q You
Journal:  Chin Med J (Engl)       Date:  1987-09       Impact factor: 2.628

8.  Effect of combined treatment with praziquantel and artemether on Schistosoma japonicum and Schistosoma mansoni in experimentally infected animals.

Authors:  J Utzinger; J Chollet; J You; J Mei; M Tanner; S Xiao
Journal:  Acta Trop       Date:  2001-09-01       Impact factor: 3.112

9.  Stability and reproductive fitness of Schistosoma mansoni isolates with decreased sensitivity to praziquantel.

Authors:  S William; A Sabra; F Ramzy; M Mousa; Z Demerdash; J L Bennett; T A Day; S Botros
Journal:  Int J Parasitol       Date:  2001-08       Impact factor: 3.981

10.  Reduced susceptibility to praziquantel among naturally occurring Kenyan isolates of Schistosoma mansoni.

Authors:  Sandra D Melman; Michelle L Steinauer; Charles Cunningham; Laura S Kubatko; Ibrahim N Mwangi; Nirvana Barker Wynn; Martin W Mutuku; Diana M S Karanja; Daniel G Colley; Carla L Black; William Evan Secor; Gerald M Mkoji; Eric S Loker
Journal:  PLoS Negl Trop Dis       Date:  2009-08-18
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  11 in total

1.  Evaluation of the schistosomicidal activity of the steroidal alkaloids from Solanum lycocarpum fruits.

Authors:  Mariza Abreu Miranda; Lizandra Guidi Magalhães; Renata Fabiane Jorge Tiossi; Christian Collins Kuehn; Luiz Gustavo Rodrigues Oliveira; Vanderlei Rodrigues; James Dewey McChesney; Jairo Kenupp Bastos
Journal:  Parasitol Res       Date:  2012-01-27       Impact factor: 2.289

Review 2.  A review of dihydroartemisinin as another gift from traditional Chinese medicine not only for malaria control but also for schistosomiasis control.

Authors:  Xu-Guang Zhang; Gui-Xin Li; Shu-Shun Zhao; Fu-Liang Xu; Yun-Hai Wang; Wei Wang
Journal:  Parasitol Res       Date:  2014-03-08       Impact factor: 2.289

Review 3.  Present-day anthelmintics and perspectives on future new targets.

Authors:  Amira Taman; Manar Azab
Journal:  Parasitol Res       Date:  2014-06-04       Impact factor: 2.289

4.  Effect of ozonide OZ418 against Schistosoma japonicum harbored in mice.

Authors:  Jian Xue; Xiaofang Wang; Yuxiang Dong; Jonathan L Vennerstrom; Shu-hua Xiao
Journal:  Parasitol Res       Date:  2014-06-20       Impact factor: 2.289

5.  Is there a reduced sensitivity of dihydroartemisinin against praziquantel-resistant Schistosoma japonicum?

Authors:  Wei Wang; Hong-Jun Li; Guo-Li Qu; Yun-Tian Xing; Zhen-Kun Yang; Jian-Rong Dai; You-Sheng Liang
Journal:  Parasitol Res       Date:  2013-10-22       Impact factor: 2.289

6.  Dihydroartemisinin: a new story of an old drug against Schistosoma mansoni infection.

Authors:  Hong-Jun Li; Fu-Liang Xu; Yun-Hai Wang; Zheng-Jun Yi; Wei Wang
Journal:  Parasitol Res       Date:  2013-10-22       Impact factor: 2.289

7.  A penta-substituted pyridine alkaloid from the rhizome of Jatropha elliptica (Pohl) Muell. Arg. is active against Schistosoma mansoni and Biomphalaria glabrata.

Authors:  Aldenir Feitosa dos Santos; Saskya Araújo Fonseca; Fernanda Andrade César; Mônica Camelo Pessoa de Azevedo Albuquerque; José Valfrido Santana; Antônio Euzébio Goulart Santana
Journal:  Parasitol Res       Date:  2014-02-06       Impact factor: 2.289

Review 8.  Repurposing drugs for the treatment and control of helminth infections.

Authors:  Gordana Panic; Urs Duthaler; Benjamin Speich; Jennifer Keiser
Journal:  Int J Parasitol Drugs Drug Resist       Date:  2014-07-30       Impact factor: 4.077

9.  Natural products as leads in schistosome drug discovery.

Authors:  Bruno J Neves; Carolina H Andrade; Pedro V L Cravo
Journal:  Molecules       Date:  2015-01-23       Impact factor: 4.411

10.  Epiisopilosine alkaloid has activity against Schistosoma mansoni in mice without acute toxicity.

Authors:  Maria A Guimarães; Rosimeire N de Oliveira; Rebeca L de Almeida; Ana C Mafud; Ana L V Sarkis; Rayane Ganassin; Marcos P da Silva; Daniel B Roquini; Leiz M Veras; Tânia C H Sawada; Cristina D Ropke; Luis A Muehlmann; Graziella A Joanitti; Selma A S Kuckelhaus; Silmara M Allegretti; Yvonne P Mascarenhas; Josué de Moraes; José R S A Leite
Journal:  PLoS One       Date:  2018-05-11       Impact factor: 3.240

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