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首页> 外文期刊>Restorative neurology and neuroscience >Different neuroprotection and therapeutic time windows by two specific diazepam regimens on retinal ganglion cells after optic nerve transection in adult rats
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Different neuroprotection and therapeutic time windows by two specific diazepam regimens on retinal ganglion cells after optic nerve transection in adult rats

机译:成年大鼠视神经横断后两种特定地西two对视网膜神经节细胞的不同神经保护和治疗时间窗

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Purpose: To compare neuroprotection and therapeutic time windows of two diazepam regimens on retinal ganglion cells (RGCs) after rat optic nerve transection (ONT). Methods: Adult rats received initial intraperitoneal diazepam injections 30 minutes before left ONT, followed by daily diazepam (Regimen-A) or every 8 hours for 3 days (Regimen-B) until they were killed at Day 7 or 14. Initial diazepam in Regimen-A and Regimen-B was delayed to 3, 6, 7, 9, 10, 12 and 6, 7, 8, 9, 10, 12 hours after ONT and these animals survived for 7 days. The effect of daily combinational uses of diazepam and bicuculline was assayed at 7 days. Results: Regimen-A induced higher RGC densities than those in control and Regimen-B groups at Day 7, but lower density than Regimen-B did at Day 14. When initial diazepam was delayed beyond 6 or 8 hours after ONT with Regimen-A and Regimen-B, the promoting effects of diazepam on RGC densities disappeared. Bicuculline completely inhibited the protection of diazepam. Conclusions: Prolonged neuroprotection on RGCs at Day 14 and extended therapeutic time window for 8 hours can be achieved by Regimen-B, while Regimen-A induces a stronger neuroprotection at Day 7. Diazepam neuroprotection is mediated through GABA A receptor.
机译:目的:比较大鼠视神经横断(ONT)后两种地西epa对视网膜神经节细胞(RGC)的神经保护作用和治疗时间窗。方法:成年大鼠在离开ONT前30分钟接受腹膜内地西epa初始注射,然后每天进行地西epa(Regimen-A)或每8小时3天(Regimen-B)注射,直到在第7天或第14天被杀死。 -A和方案-B延迟到ONT后3、6、7、9、10、12和6、7、8、9、10、12小时,这些动物存活7天。在第7天测定了地西epa和双瓜氨酸的每日组合使用的效果。结果:在第7天,方案A诱导的RGC密度高于对照组和方案B组,但在第14天则比方案B降低。当初始地西epa被延迟使用ONT后,方案6或8小时。和Regimen-B,地西epa对RGC密度的促进作用消失了。 Bicuculline完全抑制了地西epa的保护。结论:Regimen-B在第14天对RGC的神经保护作用延长,治疗时间窗延长8小时,而Regimen-A在第7天诱导更强的神经保护作用。地西am的神经保护作用是通过GABA A受体介导的。

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