Cognitive Dysfunction in Mice Infected withPlasmodium bergheiStrain ANKA

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Cerebral malaria complicated by cognitive sequelae is a major cause of morbidity in humans infected withPlasmodium falciparum.To model cognitive function after malaria, we created a rodent model of cerebral malaria by infecting C57BL/6 mice withPlasmodium bergheistrainANKA. After 7 days, an object-recognition test of working memory revealed a significant impairment in the visual memory of infected mice. This impairment was observed in the absence of confounding effects of infection. The cognitive dysfunction correlated with hemorrhage and inflammation. Furthermore, microglial activity and morphological changes detected throughout the brains of infected mice were absent from the brains of control mice, and this correlated with the measured cognitive defects. Similar testing methods in human studies could help identify subjects at risk for an adverse cognitive outcome. This murine model should facilitate the study of adjunctive methods to ameliorate adverse neurological outcomes in cerebral malaria.

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