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新生大鼠脑卒中模型中水通道蛋白4表达及磁共振成像的时间和区域演变

Temporal and regional evolution of aquaporin-4 expression and magnetic resonance imaging in a rat pup model of neonatal stroke.

作者信息

Badaut Jérôme, Ashwal Stephen, Tone Beatriz, Regli Luca, Tian Hou Rou, Obenaus Andre

机构信息

Neurosurgery Research Group, Centre Hospitalier Universitaire Vaudois, Pavilion 3-Beaumont, 1011 Lausanne, Switzerland.

出版信息

Pediatr Res. 2007 Sep;62(3):248-54. doi: 10.1203/PDR.0b013e3180db291b.

Abstract

Edema formation can be observed using magnetic resonance imaging (MRI) in patients with stroke. Recent studies have shown that aquaporin-4 (AQP4), a water channel, is induced early after stroke and potentially participates in the development of brain edema. We studied whether induction of AQP4 correlated with edema formation in a rat pup filament stroke model using high field (11.7-Tesla) MRI followed by immunohistochemical investigation of AQP4 protein expression. At 24 h, we observed increased T2 values and decreased apparent diffusion coefficients (ADC) within injured cortical and striatal regions that reflected the edema formation. Coincident with these MR changes were significant increases in AQP4 expression on astrocytic end-feet in the border regions of injured tissues. Striatal imaging findings were still present at 72 h with a slow normalization of AQP4 expression in the border regions. At 28 d, AQP4 expression normalized in the border while in this region ADC values increased. We show that induction of AQP4 is increased during the period of active edema formation in the border region without regional correlation with edema. Finally, induction of AQP4 on astrocyte end-feet could participate in tissue preservation after ischemia in the immature rat brain.

摘要

在中风患者中,可通过磁共振成像(MRI)观察到水肿形成。最近的研究表明,水通道蛋白4(AQP4)作为一种水通道,在中风后早期被诱导产生,并可能参与脑水肿的发展。我们使用高场(11.7特斯拉)MRI,随后对AQP4蛋白表达进行免疫组织化学研究,以探讨在大鼠幼崽线栓性中风模型中,AQP4的诱导与水肿形成是否相关。在24小时时,我们观察到损伤的皮质和纹状体区域内T2值升高,表观扩散系数(ADC)降低,这反映了水肿的形成。与这些磁共振变化同时出现的是,损伤组织边缘区域星形胶质细胞终足上的AQP4表达显著增加。在72小时时,纹状体成像结果仍然存在,边缘区域的AQP4表达缓慢恢复正常。在28天时,边缘区域的AQP4表达恢复正常,而该区域的ADC值增加。我们发现,在边缘区域活跃的水肿形成期,AQP4的诱导增加,且与水肿无区域相关性。最后,星形胶质细胞终足上AQP4的诱导可能参与未成熟大鼠脑缺血后的组织保护。

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