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Reprod Toxicol ; 89: 107-114, 2019 10.
Article in English | MEDLINE | ID: mdl-31310803

ABSTRACT

Malaria in pregnant women is associated with risk of maternal and perinatal morbidity and mortality, and there are few antimalarial drugs considered safe to treat them, so it is necessary to develop safer antimalarial medicines. The goal of this study was to develop an animal model for human malaria during pregnancy by characterizing the maternal and fetal outcomes in malaria infected Swiss mice. For that, in the present study, we evaluated the outcome of pregnancy in Swiss mice infected with Plasmodium berghei ANKAGFP. We observed a reduction of fetal body weight and signs of skeletal ossification retardation in the offspring of mice infected on GD 12. The group of mice infected with malaria presented premature deliveries and histopathology changes consistent with placental malaria. Our study suggests that Swiss Webster mice infected with P. berghei ANKAGFP on GD 12 might be a valuable model to investigate the safety and the efficacy of new antimalarial drugs indicated to pregnant women.


Subject(s)
Antimalarials/therapeutic use , Fetal Development/drug effects , Fetal Growth Retardation/prevention & control , Malaria/drug therapy , Plasmodium berghei/drug effects , Pregnancy Complications, Parasitic/drug therapy , Animals , Animals, Newborn , Antimalarials/administration & dosage , Disease Models, Animal , Female , Fetal Growth Retardation/parasitology , Gestational Age , Malaria/parasitology , Plasmodium berghei/growth & development , Pregnancy , Pregnancy Complications, Parasitic/parasitology , Pregnancy Outcome
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