首页> 外文期刊>Brain research >Pilocarpine-induced seizure-like activity with increased BNDF and neuropeptide Y expression in organotypic hippocampal slice cultures.
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Pilocarpine-induced seizure-like activity with increased BNDF and neuropeptide Y expression in organotypic hippocampal slice cultures.

机译:毛果芸香碱诱导的癫痫样活动,在器官型海马切片培养物中增加了BNDF和神经肽Y的表达。

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Organotypic hippocampal slice cultures were treated with the muscarinic agonist pilocarpine to study induced seizure-like activity and changes in neurotrophin and neuropeptide expression. For establishment of a seizure-inducing protocol, 2-week-old cultures derived from 6-8-day-old rats were exposed to 0.1 mM to 5 mM of pilocarpine for 4 h to 7 days. Other cultures were treated with pilocarpine for 7 days and left for 7-14 days in normal medium. Age-matched, non-treated cultures served as controls. Intracellular recordings from CA1 pyramidal cells revealed increased spontaneous activity in 31 of 35 cultures superfused with 0.1 or 5 mM pilocarpine. Epileptiform discharges were recorded in 17 of the 31 cultures, and 19 displayed frequencies specifically in the 6-12-Hz (Theta rhythm) range when superfused with pilocarpine. The pilocarpine effect was blocked by simultaneous superfusion with the muscarinic receptor antagonist atropine (100 microM). Regardless of dose and exposure time, the pilocarpine treatment induced very limited neuronal cell death, recorded as cellular propidium iodide uptake. Cultures exposed to 5 mM pilocarpine for up to 7 days displayed increased BDNF expression when analyzed by Western blot and ELISA. This BDNF increase correlated with increased neuropeptide Y immunoreactivity, known to accompany seizure activity. Addition of BDNF (200 ng/ml) to otherwise untreated cultures also upregulated NPY expression. The pilocarpine-induced seizure-like activity in hippocampal slice cultures, with concomitant increase in BDNF and NPY expression, is compared with in vivo observations and discussed in terms of the potential use of the easily accessible slice cultures in experimental seizure research.
机译:用毒蕈碱激动剂毛果芸香碱处理器官型海马切片培养物,以研究诱导的癫痫样活动以及神经营养蛋白和神经肽表达的变化。为了建立诱发癫痫的方法,将来自6-8天龄大鼠的2周龄培养物暴露于0.1 mM至5 mM毛果芸香碱4 h至7天。其他培养物用毛果芸香碱处理7天,然后在正常培养基中放置7-14天。年龄匹配的未处理培养物作为对照。 CA1锥体细胞的细胞内记录显示,在融合了0.1或5 mM毛果芸香碱的35种培养物中,有31种的自发活性增加。在31种培养物中的17种中记录了癫痫样放电,当与毛果芸香碱融合时,有19种显示的频率在6-12 Hz(θ节奏)范围内。通过同时与毒蕈碱受体拮抗剂阿托品(100 microM)融合来阻断毛果芸香碱的作用。不论剂量和暴露时间如何,毛果芸香碱治疗均引起非常有限的神经元细胞死亡,记录为细胞对碘化丙锭的摄取。当通过蛋白质印迹和ELISA分析时,暴露于5mM毛果芸香碱长达7天的培养物显示出增加的BDNF表达。 BDNF的增加与已知伴随癫痫发作活动的神经肽Y免疫反应性增加有关。向未经处理的培养物中添加BDNF(200 ng / ml)也会上调NPY表达。将海马切片培养物中毛果芸香碱诱发的癫痫样活动与BDNF和NPY表达的增加相结合,与体内观察结果进行了比较,并讨论了易于获取的切片培养物在实验性癫痫研究中的潜在用途。

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