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盐酸瑞吡坦(BAYx3702)对缺血性中风的神经保护特性综述。

A review of the neuroprotective properties of the 5-HT1A receptor agonist repinotan HCl (BAYx3702) in ischemic stroke.

作者信息

Berends A C, Luiten P G M, Nyakas C

机构信息

Department of Molecular Neurobiology, Graduate School of Behavioral and Cognitive Neurosciences, University of Groningen, P.O. Box 149750 AA Haren, The Netherlands.

出版信息

CNS Drug Rev. 2005 Winter;11(4):379-402. doi: 10.1111/j.1527-3458.2005.tb00055.x.

Abstract

Repinotan HCl (repinotan, BAYx3702), a highly selective 5-HT1A receptor agonist with a good record of safety was found to have pronounced neuroprotective effects in experimental models that mimic various aspects of brain injury. Repinotan caused strong, dose-dependent infarct reductions in permanent middle cerebral artery occlusion, transient middle cerebral artery occlusion, and traumatic brain injury paradigms. The specific 5-HT1A receptor antagonist WAY 100635 blocked these effects, indicating that the neuroprotective properties of repinotan are mediated through the 5-HT1A receptor. The proposed neuroprotective mechanisms of repinotan are thought to be the result of neuronal hyperpolarization via the activation of G protein-coupled inwardly rectifying K+ channels upon binding to both pre- and post-synaptic 5-HT1A receptors. Hyperpolarization results in inhibition of neuron firing and reduction of glutamate release. These mechanisms, leading to protection of neurons against overexcitation, could explain the neuroprotective efficacy of repinotan per se, but not necessarily the efficacy by delayed administration. The therapeutic time window of repinotan appeared to be at least 5 h in in vivo animal models, but may be even longer at higher doses of the drug. Experimental studies indicate that repinotan affects various mechanisms involved in the pathogenesis of brain injury. In addition to the direct effect of repinotan on neuronal hyperpolarization and suppression of glutamate release this compound affects the death-inhibiting protein Bcl-2, serotonergic glial growth factor S-100beta and Nerve Growth Factor. It also suppresses the activity of caspase-3 through MAPK and PKCalpha; this effect may contribute to its neuroprotective efficacy. The dose- and time-dependent neuroprotective efficacy of repinotan indicates that the drug is a promising candidate for prevention of secondary brain damage in brain-injured patients suffering from acute ischemic stroke. Unfortunately, however, the first, randomized, double blind, placebo-controlled clinical trial did not demonstrate the efficacy of repinotan in acute ischemic stroke.

摘要

盐酸瑞匹诺坦(瑞匹诺坦,BAYx3702)是一种具有良好安全记录的高选择性5-HT1A受体激动剂,在模拟脑损伤各个方面的实验模型中被发现具有显著的神经保护作用。在永久性大脑中动脉闭塞、短暂性大脑中动脉闭塞和创伤性脑损伤模型中,瑞匹诺坦可引起强烈的、剂量依赖性的梗死灶缩小。特异性5-HT1A受体拮抗剂WAY 100635可阻断这些作用,表明瑞匹诺坦的神经保护特性是通过5-HT1A受体介导的。瑞匹诺坦拟议的神经保护机制被认为是在与突触前和突触后5-HT1A受体结合后,通过激活G蛋白偶联内向整流钾通道导致神经元超极化的结果。超极化导致神经元放电抑制和谷氨酸释放减少。这些机制可保护神经元免受过度兴奋,这可以解释瑞匹诺坦本身的神经保护功效,但不一定能解释延迟给药的功效。在体内动物模型中,瑞匹诺坦的治疗时间窗似乎至少为5小时,但在更高剂量的药物时可能更长。实验研究表明,瑞匹诺坦影响脑损伤发病机制中的各种机制。除了瑞匹诺坦对神经元超极化和谷氨酸释放抑制的直接作用外,该化合物还影响死亡抑制蛋白Bcl-2、血清素能神经胶质生长因子S-100β和神经生长因子。它还通过MAPK和PKCalpha抑制caspase-3的活性;这种作用可能有助于其神经保护功效。瑞匹诺坦的剂量和时间依赖性神经保护功效表明,该药物是预防急性缺血性中风脑损伤患者继发性脑损伤的有希望的候选药物。然而,不幸的是,第一项随机、双盲、安慰剂对照临床试验并未证明瑞匹诺坦在急性缺血性中风中的疗效。

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