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Posttraumatic reduction of edema with aquaporin-4 RNA interference improves acute and chronic functional recovery

机译:Aquaporin-4 RNA干扰在创伤后减轻水肿改善了急性和慢性功能恢复

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摘要

Traumatic brain injury (TBI) is common in young children and adolescents and is associated with long-term disability and mortality. The neuropathologic sequelae that result from juvenile TBI are a complex cascade of events that include edema formation and brain swelling. Brain aquaporin-4 (AQP4) has a key role in edema formation. Thus, development of novel treatments targeting AQP4 to reduce edema could lessen the neuropathologic sequelae. We hypothesized that inhibiting AQP4 expression by injection of small-interfering RNA (siRNA) targeting AQP4 (siAQP4) after juvenile TBI would decrease edema formation, neuroinflammation, neuronal cell death, and improve neurologic outcomes. The siAQP4 or a RNA-induced silencing complex (RISC)-free control siRNA (siGLO) was injected lateral to the trauma site after controlled cortical impact in postnatal day 17 rats. Magnetic resonance imaging, neurologic testing, and immunohistochemistry were performed to assess outcomes. Pups treated with siAQP4 showed acute (3 days after injury) improvements in motor function and in spatial memory at long term (60 days after injury) compared with siGLO-treated animals. These improvements were associated with decreased edema formation, increased microglial activation, decreased blood–brain barrier disruption, reduced astrogliosis and neuronal cell death. The effectiveness of our treatment paradigm was associated with a 30% decrease in AQP4 expression at the injection site.
机译:颅脑外伤(TBI)在幼儿和青少年中很常见,并且与长期残疾和死亡率有关。少年TBI引起的神经病理后遗症是一系列复杂的事件,包括水肿形成和脑肿胀。脑水通道蛋白4(AQP4)在水肿形成中起关键作用。因此,开发针对AQP4减轻水肿的新疗法可以减轻神经病理学后遗症。我们假设,在青少年TBI后通过注射靶向AQP4(siAQP4)的小干扰RNA(siRNA)来抑制AQP4的表达将减少水肿形成,神经炎症,神经元细胞死亡并改善神经功能。在出生后第17天的大鼠中,在受到皮质控制后,将siAQP4或无RNA诱导沉默复合物(RISC)的对照siRNA(siGLO)注射到创伤部位的侧面。进行磁共振成像,神经系统检查和免疫组织化学以评估结果。与siGLO治疗的动物相比,用siAQP4处理的幼犬长期(损伤后60天)显示出运动功能(空间方面的急性改善)和长期(损伤后60天)的空间记忆。这些改善与减少水肿形成,增加小胶质细胞活化,减少血脑屏障破坏,减少星形胶质细胞增多症和神经元细胞死亡有关。我们的治疗范例的有效性与注射部位AQP4表达下降30%有关。

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