在高岭土诱发的大鼠沟通性脑积水模型中,脑脊液流出阻力升高与脑脊液淋巴吸收受损有关。

Gurjit Nagra, Mark E Wagshul, Shams Rashid, Jie Li, J Pat McAllister, Miles Johnston
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引用次数: 0

摘要

背景:我们最近报道了高岭土模型大鼠沟通性脑积水的淋巴脑脊液(CSF)吸收障碍,脑室扩张与淋巴功能障碍的程度呈负相关。然而,如果其他部位的吸收弥补了淋巴功能的缺陷,那么脑脊液引流可能不会发生显著改变。本研究的目的是调查淋巴吸收缺陷对整体 CSF 吸收(CSF 流出阻力)的影响:方法:向 Sprague Dawley 大鼠的基底腔注射高岭土。方法:将高岭土注射到 Sprague Dawley 大鼠的基底池中,使用磁共振成像(MRI)评估脑积水的发展情况。在注射后约 3 周的一组动物中,脑室内注射的碘化人血清白蛋白(125I-HSA)进入嗅鼻甲的运动情况可估算 CSF 通过楔形板进入鼻腔淋巴管的运输情况(n = 18)。对照组动物用生理盐水代替高岭土(n = 10)。第二组动物在注射高岭土约 3.5 周后,在以不同流速向脊髓蛛网膜下腔输注生理盐水的过程中连续测量脑室内压力(n = 9)。根据稳态压力与流速的斜率计算 CSF 流出阻力。该组的对照组动物要么没有接受注射(完好无损:n = 11),要么接受生理盐水代替高岭土(n = 8):结果:与注射生理盐水的对照组相比,高岭土组的侧脑室容积明显增大(0.087 +/- 0.013 ml,n = 27 对 0.015 +/- 0.001 ml,n = 17),淋巴功能明显降低(2.14 +/- 0.72% 注射/g,n = 18 对 6.38 +/- 0.60% 注射/g,n = 10)。此外,高岭土组的 CSF 流出阻力(0.46 +/- 0.04 cm H2O microL(-1) min,n = 9)明显高于注射生理盐水组(0.28 +/- 0.03 cm H2O microL(-1) min,n = 8)或完整动物组(0.18 +/- 0.03 cm H2O microL(-1) min,n = 11)。脑脊液流出阻力与心室容积呈明显正相关:数据表明,在高岭土诱导的交流性脑积水模型中,淋巴 CSF 吸收障碍对整体 CSF 吸收有重大影响。淋巴CSF吸收障碍似乎在脑室肥大的发病机制中扮演了某种角色(直接或间接)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Elevated CSF outflow resistance associated with impaired lymphatic CSF absorption in a rat model of kaolin-induced communicating hydrocephalus.

Elevated CSF outflow resistance associated with impaired lymphatic CSF absorption in a rat model of kaolin-induced communicating hydrocephalus.

Elevated CSF outflow resistance associated with impaired lymphatic CSF absorption in a rat model of kaolin-induced communicating hydrocephalus.

Elevated CSF outflow resistance associated with impaired lymphatic CSF absorption in a rat model of kaolin-induced communicating hydrocephalus.

Background: We recently reported a lymphatic cerebrospinal fluid (CSF) absorption deficit in a kaolin model of communicating hydrocephalus in rats with ventricular expansion correlating negatively with the magnitude of the impediment to lymphatic function. However, it is possible that CSF drainage was not significantly altered if absorption at other sites compensated for the lymphatic defect. The purpose of this study was to investigate the impact of the lymphatic absorption deficit on global CSF absorption (CSF outflow resistance).

Methods: Kaolin was injected into the basal cisterns of Sprague Dawley rats. The development of hydrocephalus was assessed using magnetic resonance imaging (MRI). In one group of animals at about 3 weeks after injection, the movement of intraventricularly injected iodinated human serum albumin (125I-HSA) into the olfactory turbinates provided an estimate of CSF transport through the cribriform plate into nasal lymphatics (n = 18). Control animals received saline in place of kaolin (n = 10). In a second group at about 3.5 weeks after kaolin injection, intraventricular pressure was measured continuously during infusion of saline into the spinal subarachnoid space at various flow rates (n = 9). CSF outflow resistance was calculated as the slope of the steady-state pressure versus flow rate. Control animals for this group either received no injections (intact: n = 11) or received saline in place of kaolin (n = 8).

Results: Compared to saline injected controls, lateral ventricular volume in the kaolin group was significantly greater (0.087 +/- 0.013 ml, n = 27 versus 0.015 +/- 0.001 ml, n = 17) and lymphatic function was significantly less (2.14 +/- 0.72% injected/g, n = 18 versus 6.38 +/- 0.60% injected/g, n = 10). Additionally, the CSF outflow resistance was significantly greater in the kaolin group (0.46 +/- 0.04 cm H2O microL(-1) min, n = 9) than in saline injected (0.28 +/- 0.03 cm H2O microL(-1) min, n = 8) or intact animals (0.18 +/- 0.03 cm H2O microL(-1) min, n = 11). There was a significant positive correlation between CSF outflow resistance and ventricular volume.

Conclusions: The data suggest that the impediment to lymphatic CSF absorption in a kaolin-induced model of communicating hydrocephalus has a significant impact on global CSF absorption. A lymphatic CSF absorption deficit would appear to play some role (either direct or indirect) in the pathogenesis of ventriculomegaly.

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