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本文引用的文献

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Improved Neuroimaging Findings and Cognitive Function in a Case of High-altitude Cerebral Edema.高原脑水肿病例的神经影像学改善和认知功能变化
Intern Med. 2021 Apr 15;60(8):1299-1302. doi: 10.2169/internalmedicine.5747-20. Epub 2020 Nov 23.
2
Tracking Calcium Dynamics and Immune Surveillance at the Choroid Plexus Blood-Cerebrospinal Fluid Interface.追踪脉络丛血脑屏障界面处的钙动力学和免疫监视。
Neuron. 2020 Nov 25;108(4):623-639.e10. doi: 10.1016/j.neuron.2020.08.024. Epub 2020 Sep 21.
3
MR diffusion changes in the perimeter of the lateral ventricles demonstrate periventricular injury in post-hemorrhagic hydrocephalus of prematurity.磁共振扩散改变在侧脑室周围区域显示早产儿出血后脑积水的脑室周围损伤。
Neuroimage Clin. 2019;24:102031. doi: 10.1016/j.nicl.2019.102031. Epub 2019 Oct 8.
4
Distribution of Aquaporins 1 and 4 in the Central Nervous System.水通道蛋白1和4在中枢神经系统中的分布
Curr Health Sci J. 2019 Apr-Jun;45(2):218-226. doi: 10.12865/CHSJ.45.02.14. Epub 2019 Jun 30.
5
Acute and Evolving MRI of High-Altitude Cerebral Edema: Microbleeds, Edema, and Pathophysiology.高海拔性脑水肿的急性与进展性 MRI:微出血、水肿与病理生理学。
AJNR Am J Neuroradiol. 2019 Mar;40(3):464-469. doi: 10.3174/ajnr.A5897. Epub 2019 Jan 24.
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Emerging Roles of Vascular Endothelium in Metabolic Homeostasis.血管内皮细胞在代谢稳态中的新角色。
Circ Res. 2018 Aug 3;123(4):477-494. doi: 10.1161/CIRCRESAHA.118.313237.
7
Combined effects of aquaporin-4 and hypoxia produce age-related hydrocephalus.水通道蛋白-4 和缺氧的联合作用导致与年龄相关的脑积水。
Biochim Biophys Acta Mol Basis Dis. 2018 Oct;1864(10):3515-3526. doi: 10.1016/j.bbadis.2018.08.006. Epub 2018 Aug 8.
8
Impact of transporters and enzymes from blood-cerebrospinal fluid barrier and brain parenchyma on CNS drug uptake.血脑屏障和脑实质中的转运体和酶对中枢神经系统药物摄取的影响。
Expert Opin Drug Metab Toxicol. 2018 Sep;14(9):961-972. doi: 10.1080/17425255.2018.1513493. Epub 2018 Sep 5.
9
Blood Exposure Causes Ventricular Zone Disruption and Glial Activation In Vitro.血液暴露导致体外脑室区破坏和神经胶质细胞激活。
J Neuropathol Exp Neurol. 2018 Sep 1;77(9):803-813. doi: 10.1093/jnen/nly058.
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Chemokine and cytokine levels in the lumbar cerebrospinal fluid of preterm infants with post-hemorrhagic hydrocephalus.早产儿出血后脑积水患者腰椎脑脊液中趋化因子和细胞因子水平。
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缺氧对血脑、血脑脊液和脑脊液脑屏障的影响。

The impact of hypoxia on blood-brain, blood-CSF, and CSF-brain barriers.

机构信息

Department of Radiology, Hotchkiss Brain Institute, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.

Department of Clinical Neurosciences, Hotchkiss Brain Institute, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.

出版信息

J Appl Physiol (1985). 2021 Sep 1;131(3):977-985. doi: 10.1152/japplphysiol.00108.2020. Epub 2021 Jul 15.

DOI:10.1152/japplphysiol.00108.2020
PMID:34264124
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8461807/
Abstract

The blood-brain barrier (BBB), blood-cerebrospinal fluid (CSF) barrier (BCSFB), and CSF-brain barriers (CSFBB) are highly regulated barriers in the central nervous system comprising complex multicellular structures that separate nerves and glia from blood and CSF, respectively. Barrier damage has been implicated in the pathophysiology of diverse hypoxia-related neurological conditions, including stroke, multiple sclerosis, hydrocephalus, and high-altitude cerebral edema. Much is known about the damage to the BBB in response to hypoxia, but much less is known about the BCSFB and CSFBB. Yet, it is known that these other barriers are implicated in damage after hypoxia or inflammation. In the 1950s, it was shown that the rate of radionucleated human serum albumin passage from plasma to CSF was five times higher during hypoxic than normoxic conditions in dogs, due to BCSFB disruption. Severe hypoxia due to administration of the bacterial toxin lipopolysaccharide is associated with disruption of the CSFBB. This review discusses the anatomy of the BBB, BCSFB, and CSFBB and the impact of hypoxia and associated inflammation on the regulation of those barriers.

摘要

血脑屏障(BBB)、血脑脊液屏障(BCSFB)和脑脊液脑屏障(CSFBB)是中枢神经系统中高度调节的屏障,由复杂的多细胞结构组成,分别将神经和神经胶质与血液和脑脊液隔开。屏障损伤与多种与缺氧相关的神经疾病的病理生理学有关,包括中风、多发性硬化症、脑积水和高原脑水肿。人们对缺氧引起的 BBB 损伤了解很多,但对 BCSFB 和 CSFBB 了解甚少。然而,已知这些其他屏障在缺氧或炎症后也与损伤有关。20 世纪 50 年代,人们发现由于 BCSFB 破坏,在缺氧条件下,放射性核标记的人血清白蛋白从血浆向脑脊液中的转移速度是正常氧条件下的五倍。由于细菌毒素脂多糖的给药导致严重缺氧,与 CSFBB 的破坏有关。这篇综述讨论了 BBB、BCSFB 和 CSFBB 的解剖结构,以及缺氧和相关炎症对这些屏障调节的影响。