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Epilepsia ; 57(7): e140-5, 2016 07.
Article in English | MEDLINE | ID: mdl-27247141

ABSTRACT

Malaria is considered a neglected disease and public health problem, affecting >200 million people worldwide. In the present study we used the Plasmodium berghei ANKA (PbA) model of experimental cerebral malaria (CM) in C57BL/6 mice. After rescue from CM and parasite clearance, animals were submitted to a seizure susceptibility test (45 days after infection) using a low dose of pentylenetetrazol (PTZ, 30 mg/kg) and monitored with use of behavioral and electroencephalography (EEG) methods. Mice rescued from CM presented a reduced latency to myoclonic and tonic-clonic seizures and an increased duration of tonic-clonic seizures. In addition, quantitative analysis of EEG revealed a decrease in relative power at beta frequency band in PbA-infected animals after PTZ injection. Our results suggest that CM may lead to increased susceptibility to seizures in mice.


Subject(s)
Convulsants/adverse effects , Disease Susceptibility/chemically induced , Epilepsy/chemically induced , Pentylenetetrazole/adverse effects , Animals , Body Weight/drug effects , Disease Models, Animal , Electroencephalography , Malaria, Cerebral/drug therapy , Male , Mice , Mice, Inbred C57BL , Plasmodium berghei/pathogenicity , Statistics, Nonparametric , Time Factors
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