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Animal models of drug-resistant epilepsy
被引:43
|作者:
Potschka, Heidrun
[1
]
机构:
[1] Univ Munich, Inst Pharmacol Toxicol & Pharm, D-80539 Munich, Germany
关键词:
drug resistance;
drug refractoriness;
pharmacoresistance;
intractability;
animal models;
6-Hz model;
kindling;
status epilepticus;
epilepsy;
TEMPORAL-LOBE EPILEPSY;
AMYGDALA-KINDLED RATS;
REFRACTORY IDIOPATHIC EPILEPSY;
PSYCHOMOTOR SEIZURE MODEL;
PHENYTOIN-RESISTANT;
ANTICONVULSANT EFFICACY;
PHARMACORESISTANT EPILEPSY;
ELECTROGRAPHIC SEIZURES;
ANTIEPILEPTIC DRUGS;
P-GLYCOPROTEIN;
D O I:
10.1684/epd.2012.0532
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Several animal models are discussed in order to outline features of difficult-to-treat or drug-resistant epilepsy. These models can be categorised as those which show a poor response to different antiepileptic drugs and those in which subgroups of drug-resistant animals are selected, based on interindividual differences. Non-responders to antiepileptic drugs have been described in the amygdala kindling model, as well as the chronic phase of post-status epilepticus models. Epileptic dogs which do not respond to standard antiepileptic drugs may serve as a translational model to provide a more clinical environment for drug testing. Drug resistance or a poor response to several antiepileptic drugs has been reported for the 6-Hz model, lamotrigine-pretreated kindled rats, pentylentetrazole-induced seizures in rats pre-exposed to pilocarpine, as well as following intrauterine exposure of rats to methylazoxymethanol. Using models to select non-responders is highly time-consuming and elaborate, limiting their use in routine drug-screening procedures. Current efforts to identify biomarkers of drug resistance may simplify the selection process, e. g. replacing several weeks of seizure monitoring by a single imaging scan. Moreover, further elucidation of mechanisms of resistance may help to design a series of ex vivo or in vitro screening procedures in order to evaluate whether a test compound is affected.
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页码:226 / 234
页数:9
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