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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Neuroprotective activity of antazoline against neuronal damage induced by limbic status epilepticus.
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Neuroprotective activity of antazoline against neuronal damage induced by limbic status epilepticus.

机译:安他唑啉对边缘性癫痫持续状态引起的神经元损伤的神经保护活性。

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摘要

Imidazoline drugs exert neuroprotective effects in cerebral ischaemia models. They also have effects against mouse cerebellar and striatal neuronal death induced by N-methyl-D-aspartate (NMDA) through the blockade of NMDA currents. Here, we investigated the effects of antazoline on NMDA toxicity and current in rat hippocampal neuronal cultures, and on an in vivo model of status epilepticus. In hippocampal cultures, antazoline (30 microM) decreased NMDA-mediated neurotoxicity and also blocked the NMDA current with voltage-dependent and fast-reversible action (inhibition by 85+/-3% at -60 mV). Status epilepticus was induced by injecting pilocarpine (200 nmol) directly into the right pyriform cortex of male adult rats. The rats then received immediately three consecutive i.p. injections at 30-min intervals of either PBS (control group) or antazoline at 10 mg/kg (low-dose group) or at 45 mg/kg (high-dose group). During the 6-h recording, status epilepticus lasted more than 200 min in all groups. In the high-dose group only, seizures completely ceased 1 h after the third injection of antazoline, then started again 1 h later. Rats were killed 1 week later, and Cresyl Violet-stained sections of their brain were analysed for damage quantification. On the ipsilateral side to the pilocarpine injection, pyriform cortex and hippocampal CA1 and CA3 areas were significantly protected in both antazoline-treated groups, whilst prepyriform and entorhinal cortices were only in the high-dose group. On the contralateral side to the pilocarpine injection, only the hippocampal CA3 area was significantly protected in the low-dose group, but all investigated structures were in the high-dose group.In conclusion, antazoline is a potent neuroprotective drug in different models of neuronal primary culture, as previously shown in striatal and cerebellar granule neurons [Neuropharmacology 39 (2000) 2244], and here in hippocampal neurons. Antazoline is also neuroprotective in vivo in the intra-pyriform pilocarpine-induced status epilepticus model.
机译:咪唑啉药物在脑缺血模型中发挥神经保护作用。它们还可以通过阻断NMDA电流来抵抗N-甲基-D-天冬氨酸(NMDA)诱导的小鼠小脑和纹状体神经元死亡。在这里,我们调查了蒽唑啉对大鼠海马神经元培养物中NMDA毒性和电流的影响,以及对癫痫持续状态的体内模型的影响。在海马培养物中,antazoline(30 microM)降低了NMDA介导的神经毒性,并且还通过电压依赖性和快速可逆的作用(在-60 mV时抑制了85 +/- 3%)阻断了NMDA电流。癫痫持续状态是通过将毛果芸香碱(200 nmol)直接注射到成年雄性大鼠的右梨形皮层中而引起的。然后大鼠立即连续接受三个腹膜内注射。 PBS(对照组)或antazoline的间隔为30分钟,剂量分别为10 mg / kg(低剂量组)或45 mg / kg(高剂量组)。在6小时的记录过程中,所有组的癫痫持续状态持续超过200分钟。仅在高剂量组中,在第三次注射安他唑啉后1小时完全停止癫痫发作,然后在1小时后再次开始癫痫发作。 1周后处死大鼠,并对其脑中Cresyl紫罗兰染色的切片进行损伤定量分析。在毛果芸香碱注射液的同侧,吡喹啉和内啡肽仅在大剂量组中被吡唑啉治疗组显着保护了梨状皮质和海马CA1和CA3区域。在毛果芸香碱注射液的对侧,低剂量组仅保护海马CA3区,但所有研究结构均在高剂量组。总之,在不同模型的神经元中,antazoline是一种有效的神经保护药。如先前在纹状体和小脑颗粒神经元中所显示的[Neuropharmacology 39(2000)2244],以及在此处的海马神经元中所示。在吡喃状毛果芸香碱诱发的癫痫持续状态模型中,蒽唑啉在体内也具有神经保护作用。

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