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脑室内注入高渗右旋糖酐可诱发脑积水:一种新型脑积水动物模型。

Intraventricular infusion of hyperosmolar dextran induces hydrocephalus: a novel animal model of hydrocephalus.

作者信息

Krishnamurthy Satish, Li Jie, Schultz Lonni, McAllister James P

机构信息

Department of Neurosurgery, Upstate Medical University, Syracuse, NY 13210, USA.

出版信息

Cerebrospinal Fluid Res. 2009 Dec 11;6:16. doi: 10.1186/1743-8454-6-16.

Abstract

BACKGROUND

Popular circulation theory of hydrocephalus assumes that the brain is impermeable to cerebrospinal fluid (CSF), and is therefore incapable of absorbing the CSF accumulating within the ventricles. However, the brain parenchyma is permeable to water due to the presence of specific ion channels as well as aquaporin channels. Thus, the movement of water into and out of the ventricles may be determined by the osmotic load of the CSF. If osmotic load determines the aqueous content of CSF in this manner, it is reasonable to hypothesize that hydrocephalus may be precipitated by pathologies and/or insults that produce sustained elevations of osmotic content within the ventricles.

METHODS

We investigated this hypothesis by manipulating the osmotic content of CSF and assaying the development of hydrocephalus in the rat brain. This was achieved by continuously infusing artificial CSF (negative control; group I), fibroblast growth factor (FGF2) solution (positive control; group II) and hyperosmotic dextran solutions (10 KD and 40 KD as experimental solutions: groups III and IV) for 12 days at 0.5 muL/h. The osmolality of the fluid infused was 307, 664, 337 and 328 mOsm/L in Groups I, II, III and IV, respectively. Magnetic resonance imaging (MRI) was used to evaluate the ventricular volumes. Analysis of variance (ANOVA) with pairwise group comparisons was done to assess the differences in ventricular volumes among the four groups.

RESULTS

Group I had no hydrocephalus. Group II, group III and group IV animals exhibited significant enlargement of the ventricles (hydrocephalus) compared to group I. There was no statistically significant difference in the size of the ventricles between groups II, III and IV. None of the animals with hydrocephalus had obstruction of the aqueduct or other parts of CSF pathways on MRI.

CONCLUSION

Infusing hyperosmolar solutions of dextran, or FGF into the ventricles chronically, resulted in ventricular enlargement. These solutions increase the osmotic load in the ventricles. Water influx (through the choroid plexus CSF secretion and/or through the brain) into the ventricles to normalize this osmotic gradient results in hydrocephalus. We need to revise the popular theory of how fluid accumulates in the ventricles at least in some forms of hydrocephalus.

摘要

背景

脑积水常见的循环理论认为,脑实质对脑脊液(CSF)不可渗透,因此无法吸收在脑室内积聚的脑脊液。然而,由于存在特定的离子通道以及水通道蛋白通道,脑实质对水是可渗透的。因此,水进出脑室的运动可能由脑脊液的渗透负荷决定。如果渗透负荷以这种方式决定脑脊液的含水量,那么合理的假设是,脑积水可能由导致脑室内渗透含量持续升高的病理状况和/或损伤引发。

方法

我们通过操纵脑脊液的渗透含量并检测大鼠脑中脑积水的发展来研究这一假设。这是通过以0.5微升/小时的速度连续输注人工脑脊液(阴性对照;第一组)、成纤维细胞生长因子(FGF2)溶液(阳性对照;第二组)和高渗葡聚糖溶液(10 KD和40 KD作为实验溶液:第三组和第四组)12天来实现的。第一组、第二组、第三组和第四组输注液体的渗透压分别为307、664、337和328毫渗量/升。使用磁共振成像(MRI)评估脑室体积。进行方差分析(ANOVA)并进行组间两两比较,以评估四组之间脑室体积的差异。

结果

第一组没有脑积水。与第一组相比,第二组、第三组和第四组动物的脑室显著扩大(脑积水)。第二组、第三组和第四组之间脑室大小没有统计学上的显著差异。所有患脑积水的动物在MRI上均未出现导水管或脑脊液通路其他部位的梗阻。

结论

长期向脑室内输注高渗葡聚糖溶液或FGF会导致脑室扩大。这些溶液增加了脑室内的渗透负荷。水流入脑室(通过脉络丛脑脊液分泌和/或通过脑实质)以平衡这种渗透梯度,从而导致脑积水。我们至少在某些形式的脑积水方面需要修正关于液体在脑室内积聚的流行理论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb1c/2801660/78f6e2b72e0a/1743-8454-6-16-1.jpg

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