5-Aminovaleric acid suppresses the development of severe seizures in the methionine sulfoximine model of mesial temporal lobe epilepsy

NEUROBIOLOGY OF DISEASE

卷:67

Article

Dhaher, Roni¹  Damisah, Eyiyemisi C.²  Wang, Helen¹  Gruenbaum, Shaun E.¹  Ong, Caroline¹  Zaveri, Hitten P.³  Gruenbaum, Benjamin F.¹  Eid, Tore¹ 

[1] Yale Univ, Dept Lab Med, Sch Med, New Haven, CT 06520 USA

[2] Yale Univ, Dept Neurosurg, Sch Med, New Haven, CT 06520 USA

[3] Yale Univ, Dept Neurol, Sch Med, New Haven, CT 06520 USA

关键词: Astrocytes;    Epileptogenesis;    GABA;    Gliosis;    Glutamate;    Glutamine;    Glutamine synthetase;    Hippocampus;   

DOI  :  10.1016/j.nbd.2014.03.006

来源: Elsevier

【 摘 要 】

Mesial temporal lobe epilepsy (MTLE) is one of the most common forms of drug-resistant, localization-related epilepsies in humans. One potential therapeutic target is the brain glutamine-glutamate-GABA metabolic pathway, which is perturbed in patients with MTLE. Loss of glutamine synthetase (GS) in astrocytes may be critically involved in this perturbation, which can be modeled by infusing the GS inhibitor methionine sulfoximine (MSO) into the entorhinal-hippocampal area in rats. Because 5-aminovaleric acid (5-AV) has been implicated in modulation of the glutamine-glutamate-GABA metabolic pathway, we hypothesized that 5-AV would alter the expression of seizures in the MSO model of MTLE. Male Sprague Dawley rats (300-330 g) were implanted with an Alzet pump placed subcutaneously in the abdominal region to release either 5-AV (0.05 mg/mL, n = 6) or phosphate buffered saline (PBS, n = 6) at a rate of 2.5 mu l/h over 28 days. Five to 7 days after surgery, all rats were implanted with an intracranial pump infusing MS0 (2.5 mg/mL; 0.25 mu l/h) unilaterally into the hippocampal formation. Following the second surgery, intracranial EEG was measured from the left and right hemispheres above the dorsal hippocampal formations for a continuous period of 21 days. The EEG was correlated with simultaneous video recordings to determine the stage of seizures according to a modified Racine scale. Five-AV-treated rats experienced a 3.5 fold reduction in the number of seizures (6.7 +/- 1.4 seizures/day) than PBS-treated rats (232 63 seizures/day) during the first 2 days following MS0 pump placement (p < 0.005). Both groups showed similar seizure frequency over days 3-21 (similar to 1 seizure/day). However, the fraction of the most severe type of seizures (Racine stages 4 and 5) increased over time in the PBS treated group, but not in the 5-AV treated group. Notably, 5-AV treated rats experienced a 2.3 and 2.6 fold lower fraction of stage 4 and 5 seizures than PBS-treated rats during the 2nd and 3rd weeks of MSO treatment respectively (p <0.05 and p < 0.001 respective to week). Five-AV markedly reduces the number of seizures initially and suppresses the development of the most severe type of seizures in the MS0 model of MTLE. These results may have implications for the therapeutic use of 5-AV in treating mesial temporal lobe seizures and for our understanding of the chemical pathology of epileptogenesis and MTLE. (C) 2014 Elsevier Inc. All rights reserved.

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