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Efficacy of Cymelarsan((R)) and Diminasan((R)) against Trypanosoma equiperdum infections in mice and horses

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dc.contributor.author Hagos, A.
dc.contributor.author Goddeeris, B. M.
dc.contributor.author Yilkal, K.
dc.contributor.author Alemu, T.
dc.contributor.author Fikru, R.
dc.contributor.author Yacob, H. T.
dc.contributor.author Feseha, G.
dc.contributor.author Claes, F.
dc.date.accessioned 2010-08-18T08:49:37Z
dc.date.available 2010-08-18T08:49:37Z
dc.date.issued 2010
dc.identifier.issn 0304-4017
dc.identifier.doi http://dx.doi.org/10.1016/j.vetpar.2010.03.041
dc.identifier.other ITG-PLA
dc.identifier.other PARAS
dc.identifier.other U-SEROL
dc.identifier.other JIF
dc.identifier.other DOI
dc.identifier.other Abstract
dc.identifier.other UPD24
dc.identifier.uri http://hdl.handle.net/10390/6264
dc.description.abstract Trypanocidal sensitivity studies were conducted to assess the efficacy of Diminazene diaceturate (Diminasan((R))) and Bis (aminoethylthio) 4-melaminophenylarsine dihydrochloride (Cymelarsan((R))) against Trypanosoma equiperdum (isolated from two mares with chronic cases of dourine) 713/943 and 834/940 Dodola strains in experimentally infected mice and horses. Diminasan((R)) at doses from 3.5mg/kg to 28mg/kg and Cymelarsan((R)) at doses of 0.25mg/kg and 0.5mg/kg body weight failed to cure any of the mice, indicating a clear dose dependent relationship in the mean time of relapse observed in mice. Indeed, mice treated with lower doses relapsed after a shorter time than mice treated with higher doses. However, mice treated with Cymelarsan((R)) at doses of 1.0mg/kg and 2.0mg/kg body weight were cured and no parasitemia was observed for 60 days. The efficacy of Cymelarsan((R)) was also tested in horses. Two groups of horses containing two animals each were infected with T. equiperdum 834/940 Dodola strain and treated with Cymelarsan((R)) at a dose rate of 0.25mg/kg and 0.5mg/kg, respectively. Cymelarsan((R)) at 0.25mg/kg and 0.5mg/kg body weight cleared parasitemia within 24h post treatment and none of the animals were found to show relapse throughout the 320 days of observation. The sensitivity of the particular trypanosome strain to Cymelarsan((R)) was also supported by the relative improvement in the mean PCV levels of horses following treatment. A statistically significant difference (p<0.01) in the mean PCV levels of horses treated with Cymelarsan((R)) was observed between day 20 at peak parasitemia and days 40 as well as 60 of observation. The mean PCV levels of horses in the control group progressively decreased within the first 60 days of post infection. Two of the horses in the control group developed chronic form of dourine manifested by genital as well as nervous signs with progressive loss of body condition within 320 days post infection. The efficacy of Cymelarsan((R)) against the chronic form of dourine was confirmed after treatment of one of the control horses with Cymelarsan((R)) at a dose rate of 0.25mg/kg body weight at day 282 post infection. It was noted that the treated horse improved overall body condition and clinical signs such as incoordination of hind legs, weakness and ventral oedema disappeared within 10 days of treatment. Thus, Cymelarsan((R)) was found to be quite effective in curing horses in acute as well as chronic form of dourine. The results obtained from the present study will be important for designing effective control measures against dourine en
dc.language English en
dc.subject Animal diseases en
dc.subject Protozoal diseases en
dc.subject Dourine en
dc.subject Trypanosoma equiperdum en
dc.subject Horses en
dc.subject Mice en
dc.subject Treatment en
dc.subject Diminazene aceturate en
dc.subject Diminasan en
dc.subject Cymelarsan en
dc.subject Efficacy en
dc.subject Drug sensitivity en
dc.subject Assessment en
dc.subject Relapses en
dc.title Efficacy of Cymelarsan((R)) and Diminasan((R)) against Trypanosoma equiperdum infections in mice and horses en
dc.type Article en
dc.citation.issue 3-4 en
dc.citation.jtitle Veterinary Parasitology en
dc.citation.volume 171 en
dc.citation.pages 200-206 en
dc.identifier.pmid http://www.ncbi.nlm.nih.gov/pubmed/20417035
dc.citation.jabbreviation Vet Parasitol en


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