Milhaud D, Rondouin G, Lerner-Natoli M, Bockaert J, Lafon-Cazal M
CNRS UPR 2580, Laboratoire de Génomique Fonctionnelle 141 rue de la Cardonille, F-34094 Montpellier 5, France.
Neuroscience. 2003;120(2):475-84. doi: 10.1016/s0306-4522(03)00268-9.
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.
咪唑啉类药物在脑缺血模型中发挥神经保护作用。它们还通过阻断N-甲基-D-天冬氨酸(NMDA)电流,对N-甲基-D-天冬氨酸诱导的小鼠小脑和纹状体神经元死亡具有保护作用。在此,我们研究了安他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体内模型的影响。在海马培养物中,安他唑啉(30微摩尔)降低了NMDA介导的神经毒性,并且还以电压依赖性和快速可逆作用阻断了NMDA电流(在-60毫伏时抑制85±3%)。通过将毛果芸香碱(200纳摩尔)直接注射到成年雄性大鼠的右侧梨状皮质来诱导癫痫持续状态。然后,大鼠立即接受连续三次腹腔注射,间隔30分钟,分别注射磷酸盐缓冲液(对照组)或10毫克/千克的安他唑啉(低剂量组)或45毫克/千克的安他唑啉(高剂量组)。在6小时的记录期间,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小时癫痫发作完全停止,然后在1小时后再次发作。1周后处死大鼠,对其脑的甲酚紫染色切片进行损伤定量分析。在毛果芸香碱注射侧的同侧,两个安他唑啉治疗组的梨状皮质、海马CA1和CA3区均得到显著保护,而前梨状皮质和内嗅皮质仅在高剂量组中得到保护。在毛果芸香碱注射侧的对侧,仅低剂量组的海马CA3区得到显著保护,但所有研究结构在高剂量组中均得到保护。总之,安他唑啉在不同的神经元原代培养模型中是一种有效的神经保护药物,如先前在纹状体和小脑颗粒神经元中所示[《神经药理学》39(2000)2244],此处是在海马神经元中。安他唑啉在梨状体内毛果芸香碱诱导的癫痫持续状态模型中在体内也具有神经保护作用。