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1.
Parasitology ; 144(7): 937-944, 2017 Jun.
Article in English | MEDLINE | ID: mdl-28270242

ABSTRACT

Alveolar echinococcosis (AE) is an emerging zoonotic disease caused by the cestode Echinococcus multilocularis. The secondary infection model of AE is based on intraperitoneal injection of disease-causing metacestodes into the peritoneal cavity of mice, which allows investigations on novel drugs or immunotherapeutical treatment options in vivo. So far, such in vivo studies assessed exclusively the parasite weight at the endpoint of a given treatment period. We here developed an ultrasound (US)-based scoring system that allows to follow-up parasite development in the living animal, and provides insights into parasite growth during the treatment phase. By this method a statistically significant difference between untreated and medicated mice with E. multilocularis infection was observed at 2 months post-infection, and the growth curve of the parasite load was described by a linear mixed model. High correlation and similar levels of variation were observed for the standard method based on parasite weight measurement, the novel US-based scoring system, as well volume segmentation by post-mortem magnetic resonance imaging. Thus, US-based scoring in the live animal has the potential to assist the 3R concept by contributing to the refinement and reduction of animal use in experimental echinococcosis.


Subject(s)
Anticestodal Agents/pharmacology , Echinococcosis/diagnostic imaging , Echinococcus multilocularis/drug effects , Magnetic Resonance Imaging , Parasite Load/methods , Ultrasonography , Albendazole/pharmacology , Animals , Disease Models, Animal , Female , Mefloquine/pharmacology , Mice , Mice, Inbred BALB C
2.
Eur J Pharmacol ; 151(1): 127-9, 1988 Jun 22.
Article in English | MEDLINE | ID: mdl-3416920

ABSTRACT

In two separate research centres the ability of RO 15-4513 to protect rats against the lethal effects of ethanol (7.5 and 15 g/kg) was investigated. In neither study did RO 15-4513 offer protection against ethanol-induced lethality or the loss of righting reflex caused by these doses of ethanol. These data fail to replicate the results of an earlier report and suggest that RO 15-4513 is unlikely to be clinically useful treating acute severe ethanol toxicity.


Subject(s)
Azides/pharmacology , Benzodiazepines/pharmacology , Ethanol/antagonists & inhibitors , Animals , Ethanol/toxicity , Male , Postural Balance/drug effects , Rats , Rats, Inbred Strains , Reflex/drug effects , Time Factors
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