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伊文思蓝从脑脊液清除进入脑膜淋巴管和颈深淋巴结的动力学。

Dynamics of Evans blue clearance from cerebrospinal fluid into meningeal lymphatic vessels and deep cervical lymph nodes.

作者信息

Maloveska Marcela, Danko Jan, Petrovova Eva, Kresakova Lenka, Vdoviakova Katarina, Michalicova Alena, Kovac Andrej, Cubinkova Veronika, Cizkova Dasa

机构信息

a Department of Anatomy, Histology and Physiology , University of Veterinary Medicine and Pharmacy in Košice , Košice , Slovak Republic.

b Institute of Neuroimmunology , Slovak Academy of Sciences , Bratislava , Slovak Republic.

出版信息

Neurol Res. 2018 May;40(5):372-380. doi: 10.1080/01616412.2018.1446282. Epub 2018 Apr 5.

Abstract

Objectives Recently, it has been confirmed, that excess fluid and waste products from the brain are drained into the cerebrospinal fluid (CSF) and afterwards cleared via the olfactory route and/or lymphatic vessels in the brain dura and corresponding extracranial lymphatic structures. Therefore, the aim of present study was to monitor time-dependent uptake of Evans blue (EB) tracer from subarachnoid space into the meningeal lymphatic vessels and extracranial lymph nodes in rats during 3 hours-12 days. Methods EB was injected into the cisterna magna of anesthetized rats and after required survival, plasma, brain dura matter and corresponding lymph nodes (cervical, thoracic and lumbar) were dissected and processed for lymphatic vessels analyses using immunofluorescence and immunohistochemistry. Furthermore, we have used sensitive ultra-high-performance liquid chromatography (UHPLC) method for the determination of EB concentrations in selected samples. Results Using a combination of imaging methods, we have detected two different types of the vascular structures in the brain dura and in deep cervical lymph nodes. The blood vessels, which were RECA-1 + positive and the lymphatic-like vessels, expressing bright intense red fluorescence of EB tracer. Subsequently, using UHPLC with UV detection, we have quantified the EB concentration in positive structures by 3 hours up to 12 days after tracer delivery. A significant increase of EB concentration was detected in deep cervical lymph nodes already at 3 hours with a peak at 1 day that decreased to about one-tenth of its peak value by 12 days. Similar pattern was detected in brain dura. On the contrary, the brain tissue and plasma were almost negative for EB tracer during all tested time periods. Conclusion Our results demonstrate the dynamic changes of EB in meningeal lymphatic vessels and in deep cervical lymph nodes, thus recapitulating the downstream outflow of intracisternally injected tracer during 3 hours-12 days via dura mater lymphatic vessels towards corresponding extracranial draining system, particularly the deep cervical lymph nodes.

摘要

目的 最近已证实,大脑中多余的液体和废物会排入脑脊液(CSF),然后通过嗅觉途径和/或脑硬脑膜中的淋巴管及相应的颅外淋巴结构清除。因此,本研究的目的是监测伊文思蓝(EB)示踪剂在3小时至12天内从大鼠蛛网膜下腔进入脑膜淋巴管和颅外淋巴结的时间依赖性摄取情况。方法 将EB注入麻醉大鼠的小脑延髓池,在所需的存活时间后,解剖血浆、脑硬脑膜和相应的淋巴结(颈、胸和腰),并使用免疫荧光和免疫组织化学方法进行淋巴管分析。此外,我们使用灵敏的超高效液相色谱(UHPLC)方法测定选定样品中的EB浓度。结果 通过结合成像方法,我们在脑硬脑膜和颈深淋巴结中检测到两种不同类型的血管结构。一种是RECA-1阳性的血管,另一种是表达EB示踪剂明亮强烈红色荧光的类淋巴管。随后,使用带有紫外检测的UHPLC,我们在示踪剂注入后3小时至12天对阳性结构中的EB浓度进行了定量。在颈深淋巴结中,3小时时就检测到EB浓度显著增加,1天时达到峰值,到12天时降至峰值的约十分之一。在脑硬脑膜中也检测到类似模式。相反,在所有测试时间段内,脑组织和血浆中的EB示踪剂几乎呈阴性。结论 我们的结果证明了EB在脑膜淋巴管和颈深淋巴结中的动态变化,从而概括了在3小时至12天内,经小脑延髓池注入的示踪剂通过硬脑膜淋巴管向相应颅外引流系统,特别是颈深淋巴结的下游流出情况。

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