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谷氨酸受体调节剂在6赫兹和最大电休克癫痫模型中的效果比较。

Comparison of the effect of glutamate receptor modulators in the 6 Hz and maximal electroshock seizure models.

作者信息

Barton Matthew E, Peters Steven C, Shannon Harlan E

机构信息

Neuroscience Research Division, Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN 46285, USA.

出版信息

Epilepsy Res. 2003 Sep;56(1):17-26. doi: 10.1016/j.eplepsyres.2003.08.001.

Abstract

Glutamatergic ionotropic and metabotropic receptor modulators have been shown to produce anticonvulsant activity in a number of animal seizure models, e.g. maximal electroshock (MES) and DBA/2 sensory-induced seizures. The 6 Hz model of partial seizures is an alternative low frequency, long duration stimulation paradigm resulting in a seizure characterized by jaw and forelimb clonus, immobility, and an elevated tail (Straub-tail). A unique aspect of this model is that it is the only acute electrically-induced seizure model in which levetiracetam has displayed anticonvulsant activity, suggesting that the 6 Hz seizure model may be useful in identifying compounds with unique anticonvulsant profiles. The purpose of the present study was to examine the role of glutamate receptors in the MES and 6 Hz seizure models using a number of NMDA, AMPA/KA, and mGlu receptor modulators. The pharmacological profile of the 6 Hz seizure model was compared to that of the MES model using eight ionotropic glutamate receptor antagonists and eight mGlu receptor modulators. The ionotropic receptor antagonists MK-801, LY235959, NBQX, LY293558, GYKI 52466, LY300168, and LY377770 produced complete protection from tonic extension in the MES model. Furthermore, the noncompetitive mGlu1 (LY456236) and mGlu5 (MPEP) metabotropic receptor antagonists and the mGlu8 metabotropic receptor agonist (PPG) were also effective in the MES model whereas the competitive mGlu1 (LY367385) receptor antagonist, the mGlu2/3 (LY379268 and LY389795) and Group III (L-AP4) metabotropic receptor agonists were ineffective. In contrast, all of the compounds tested, produced dose-dependent protection in the 6 Hz model with an increase in potency as compared to the MES model. The largest protective indices (P.I.=TD50/ED50) observed were associated with the iGlu5 antagonist LY382884 and the mGlu2/3 receptor agonists LY379268 and LY389795 (P.I.=>14, 14, and 4.9, respectively) in the 6 Hz model. The results from the present study support the continued search for glutamate receptor modulators as potential antiepileptic agents. Furthermore these results illustrate the importance of using several different animal seizure models in the search for novel AEDs and the potential utility of the 6 Hz seizure model in identifying novel AEDs.

摘要

谷氨酸能离子型和代谢型受体调节剂已在多种动物癫痫模型中显示出抗惊厥活性,例如最大电休克(MES)和DBA/2感觉诱发性癫痫。部分性癫痫的6Hz模型是一种替代性的低频、长时间刺激模式,可导致以颌部和前肢阵挛、不动以及尾巴抬高(Straub尾)为特征的癫痫发作。该模型的一个独特之处在于,它是左乙拉西坦显示出抗惊厥活性的唯一急性电诱导癫痫模型,这表明6Hz癫痫模型可能有助于鉴定具有独特抗惊厥谱的化合物。本研究的目的是使用多种NMDA、AMPA/KA和代谢型谷氨酸受体调节剂,研究谷氨酸受体在MES和6Hz癫痫模型中的作用。使用八种离子型谷氨酸受体拮抗剂和八种代谢型谷氨酸受体调节剂,将6Hz癫痫模型的药理学特征与MES模型进行比较。离子型受体拮抗剂MK-801、LY235959、NBQX、LY293558、GYKI 52466、LY300168和LY377770在MES模型中对强直伸展产生了完全保护作用。此外,非竞争性代谢型mGlu1(LY456236)和mGlu5(MPEP)受体拮抗剂以及mGlu8代谢型受体激动剂(PPG)在MES模型中也有效,而竞争性mGlu1(LY367385)受体拮抗剂、mGlu2/3(LY379268和LY389795)和III组(L-AP4)代谢型受体激动剂无效。相比之下,所有测试的化合物在6Hz模型中均产生了剂量依赖性保护作用,且与MES模型相比效力有所增加。在6Hz模型中观察到的最大保护指数(P.I.=TD50/ED50)与离子型Glu5拮抗剂LY382884以及mGlu2/3受体激动剂LY379268和LY389795相关(分别为P.I.>14、14和4.9)。本研究的结果支持继续寻找谷氨酸受体调节剂作为潜在的抗癫痫药物。此外,这些结果说明了在寻找新型抗癫痫药物时使用多种不同动物癫痫模型的重要性,以及6Hz癫痫模型在鉴定新型抗癫痫药物方面的潜在用途。

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