Cavarsan Clarissa F, Matsuo Alisson, Blanco Miriam M, Mello Luiz E
Department of Physiology, Universidade Federal de São Paulo, Pedro de Toledo St, 669, 3rd floor, 04039-032 São Paulo, SP, Brazil.
UNONEX, Department of Microbiology, Immunology, and Parasitology, Universidade Federal de São Paulo, Building Prof. Dr. Antonio C. Mattos Paiva, Botucatu St, 862, 8th floor, Vila Clementino, 04023-062 São Paulo, SP, Brazil.
Epilepsy Behav. 2015 Mar;44:90-5. doi: 10.1016/j.yebeh.2014.12.034. Epub 2015 Feb 4.
Homer1a is a protein that regulates metabotropic glutamate receptors involved in neural plasticity processes. Recently, we demonstrated that Homer1a mRNA is enhanced after pilocarpine-induced status epilepticus. Here, we investigated whether a single acute seizure triggered by means of pentylenetetrazole (PTZ) injection or maximal electroshock (MES) stimulation (2 different seizure models) would alter Homer1a expression in the hippocampus.
Male Wistar rats subjected to the PTZ or MES model were analyzed 2h, 8h, 24h, and 7days after seizure induction. Homer1a, mGluR1, and mGluR5 mRNA expression levels in hippocampal extracts were analyzed by quantitative PCR.
Quantitative PCR revealed Homer1a overexpression at 2h after MES-induced tonic-clonic seizures compared to control, but the overexpression did not remain elevated after 8h. Pentylenetetrazole-induced seizures, in contrast, were not able to change Homer1a mRNA expression. No differences were observed at these time points after seizures for mGluR1 and mGluR5 mRNA expression in any of the models.
Our data indicate that the levels of Homer1a mRNA were transiently increased only after MES-induced tonic-clonic seizures (and not after PTZ-induced seizures). We suggest that Homer1a expression may be dependent on seizure intensity or on specific brain circuit activation. We suggest that Homer1a may contribute to counteract hyperexcitability processes.
Homer1a是一种调节参与神经可塑性过程的代谢型谷氨酸受体的蛋白质。最近,我们证明毛果芸香碱诱导的癫痫持续状态后Homer1a mRNA会增强。在此,我们研究了通过注射戊四氮(PTZ)或最大电休克(MES)刺激引发的单次急性癫痫发作(两种不同的癫痫模型)是否会改变海马体中Homer1a的表达。
对接受PTZ或MES模型的雄性Wistar大鼠在癫痫发作诱导后2小时、8小时、24小时和7天进行分析。通过定量PCR分析海马提取物中Homer1a、mGluR1和mGluR5 mRNA的表达水平。
定量PCR显示,与对照组相比,MES诱导的强直阵挛性癫痫发作后2小时Homer1a过表达,但8小时后过表达不再升高。相比之下,PTZ诱导的癫痫发作未能改变Homer1a mRNA的表达。在任何模型中,癫痫发作后的这些时间点,mGluR1和mGluR5 mRNA表达均未观察到差异。
我们的数据表明,仅在MES诱导的强直阵挛性癫痫发作后(而非PTZ诱导的癫痫发作后)Homer1a mRNA水平短暂升高。我们认为Homer1a的表达可能取决于癫痫发作强度或特定脑回路激活。我们认为Homer1a可能有助于对抗过度兴奋过程。