High seizure frequency prior to antiepileptic treatment is a predictor of pharmacoresistant epilepsy in a rat model of temporal lobe epilepsy

被引:49
作者
Loescher, Wolfgang [1 ]
Brandt, Claudia
机构
[1] Univ Vet Med, Dept Pharmacol Toxicol & Pharm, D-30559 Hannover, Germany
基金
美国国家卫生研究院;
关键词
Intractable epilepsy; Hippocampal sclerosis; Antiepileptic drugs; Phenobarbital; AMYGDALA-KINDLED RATS; SUDDEN UNEXPECTED DEATH; DRUG-RESPONSIVE RATS; BLOOD-BRAIN-BARRIER; STATUS-EPILEPTICUS; REFRACTORY EPILEPSY; P-GLYCOPROTEIN; ANTICONVULSANT EFFICACY; ELECTRICAL-STIMULATION; ESTROUS-CYCLE;
D O I
10.1111/j.1528-1167.2009.02183.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
P>Purpose: Progress in the management of patients with medically intractable epilepsy is impeded because we do not fully understand why pharmacoresistance happens and how it can be predicted. The presence of multiple seizures prior to medical treatment has been suggested as a potential predictor of poor outcome. In the present study, we used an animal model of temporal lobe epilepsy to investigate whether pharmacoresistant rats differ in seizure frequency from pharmacoresponsive animals. Methods: Epilepsy with spontaneous recurrent seizures (SRS) was induced by status epilepticus. Frequency of SRS was determined by video/EEG (electroencephalography) monitoring in a total of 33 epileptic rats before onset of treatment with phenobarbital (PB). Results: Thirteen (39%) rats did not respond to treatment with PB. Before treatment with PB, average seizure frequency in PB nonresponders was significantly higher than seizure frequency in responders, which, however, was due to six nonresponders that exhibited > 3 seizures per day. Such high seizure frequency was not observed in responders, demonstrating that high seizure frequency predicts pharmacoresistance in this model, but does not occur in all nonresponders. Discussion: The data from this study are in line with clinical experience that the frequency of seizures in the early phase of epilepsy is a dominant risk factor that predicts refractoriness. However, resistance to treatment also occurred in rats that did not differ in seizure frequency from responders, indicating that disease severity alone is not sufficient to explain antiepileptic drug (AED) resistance. These data provide further evidence that epilepsy models are useful in the search for predictors and mechanisms of pharmacoresistance.
引用
收藏
页码:89 / 97
页数:9
相关论文
共 44 条
  • [1] Is refractory epilepsy preventable?
    Arroyo, S
    Brodie, MJ
    Avanzini, G
    Baumgartner, C
    Chiron, C
    Dulac, O
    French, JA
    Serratosa, JM
    [J]. EPILEPSIA, 2002, 43 (04) : 437 - 444
  • [2] Resistance to antiepileptic drugs and expression of P-glycoprotein in two rat models of status epilepticus
    Bankstahl, Jens P.
    Loescher, Wolfgang
    [J]. EPILEPSY RESEARCH, 2008, 82 (01) : 70 - 85
  • [3] Baulac M., 2002, ANTIEPILEPTIC DRUGS, P514
  • [4] Antiepileptic drug resistant rats differ from drug responsive rats in GABAA receptor subunit expression in a model of temporal lobe epilepsy
    Bethmann, Kerstin
    Fritschy, Jean-Marc
    Brandt, Claudia
    Loescher, Wolfgang
    [J]. NEUROBIOLOGY OF DISEASE, 2008, 31 (02) : 169 - 187
  • [5] Resistance to phenobarbital extends to phenytoin in a rat model of temporal lobe epilepsy
    Bethmann, Kerstin
    Brandt, Claudia
    Loescher, Wolfgang
    [J]. EPILEPSIA, 2007, 48 (04) : 816 - 826
  • [6] Striking differences in individual anticonvulsant response to phenobarbital in rats with spontaneous seizures after status epilepticus
    Brandt, C
    Volk, HA
    Löscher, W
    [J]. EPILEPSIA, 2004, 45 (12) : 1488 - 1497
  • [7] Epileptogenesis and neuropathology after different types of status epilepticus induced by prolonged electrical stimulation of the basolateral amygdala in rats
    Brandt, C
    Glien, M
    Potschka, H
    Volk, H
    Löscher, W
    [J]. EPILEPSY RESEARCH, 2003, 55 (1-2) : 83 - 103
  • [8] The multidrug transporter hypothesis of drug resistance in epilepsy:: Proof-of-principle in a rat model of temporal lobe epilepsy
    Brandt, Claudia
    Bethmann, Kerstin
    Gastens, Alexandra M.
    Loescher, Wolfgang
    [J]. NEUROBIOLOGY OF DISEASE, 2006, 24 (01) : 202 - 211
  • [9] PLASMA CONCENTRATION OF LH, FSH, PROLACTIN, PROGESTERONE AND ESTRADIOL-17BETA THROUGHOUT 4-DAY ESTROUS-CYCLE OF RAT
    BUTCHER, RL
    COLLINS, WE
    FUGO, NW
    [J]. ENDOCRINOLOGY, 1974, 94 (06) : 1704 - 1708
  • [10] Antiepileptic drug therapy: When is epilepsy truly intractable?
    Camfield, PR
    Camfield, CS
    [J]. EPILEPSIA, 1996, 37 : S60 - S65