Quantitative evaluation of blood-cerebrospinal fluid barrier permeability in the rat with experimental meningitis using magnetic resonance imaging
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作者:
Ichikawa, Hiroyuki
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Otsuka Pharmaceut Co Ltd, Inst New Drug Discovery 3, Kawaguchi, Tokushima 7710192, JapanOtsuka Pharmaceut Co Ltd, Inst New Drug Discovery 3, Kawaguchi, Tokushima 7710192, Japan
Ichikawa, Hiroyuki
[1
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Ishikawa, Makoto
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Otsuka Pharmaceut Co Ltd, Inst New Drug Discovery 3, Kawaguchi, Tokushima 7710192, JapanOtsuka Pharmaceut Co Ltd, Inst New Drug Discovery 3, Kawaguchi, Tokushima 7710192, Japan
Ishikawa, Makoto
[1
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Fukunaga, Mari
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Otsuka Pharmaceut Co Ltd, Inst New Drug Discovery 3, Kawaguchi, Tokushima 7710192, JapanOtsuka Pharmaceut Co Ltd, Inst New Drug Discovery 3, Kawaguchi, Tokushima 7710192, Japan
Fukunaga, Mari
[1
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Ishikawa, Koichi
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Gunma Univ, Inst Mol & Cellular Regulat, Maebashi, Gunma 3718512, JapanOtsuka Pharmaceut Co Ltd, Inst New Drug Discovery 3, Kawaguchi, Tokushima 7710192, Japan
Ishikawa, Koichi
[2
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Ishiyama, Hironobu
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Otsuka Pharmaceut Co Ltd, Inst New Drug Discovery 3, Kawaguchi, Tokushima 7710192, JapanOtsuka Pharmaceut Co Ltd, Inst New Drug Discovery 3, Kawaguchi, Tokushima 7710192, Japan
Ishiyama, Hironobu
[1
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[1] Otsuka Pharmaceut Co Ltd, Inst New Drug Discovery 3, Kawaguchi, Tokushima 7710192, Japan
Disruption of the blood-brain barrier (BBB) and/or the blood-cerebrospinal fluid barrier (BCSFB) is thought to be one of the major pathophysiological consequences of meningitis and contributes to the development of adverse neurological outcomes. In order to clarify this hypothesis further, we sequentially quantified the permeability of these barriers with magnetic resonance imaging (MRI) contrast enhancement using gadolinium-diethylene triamine pentaacetic acid (Gd-DTPA) in rats with various experimentally-induced meningitis. Meningeal inflammation was elicited by an intracisternal injection of interleukin (IL)-1 beta, prostaglandin (PG) E-2, or lipopolysaccharide (LPS). Barrier permeability was calculated from the gadolinium-enhancement ratio (GER) in the subarachnoid space (SAS). The secretion of Gd-DTPA into the SAS was monitored by T1-weighted imaging after an intravenous injection of Gd-DTPA. As a significant linear correlation was observed between the GER and the standard solution, the concentration of the secreted Gd-DTPA were determined from the GER. The maximal intensity in SAS was detected at 5 mm after Gd-DTPA administration and it declined gradually. Among the inflammatory agents, IL-1 beta was found to induce the most severe meningitis as determined from the GER. The concentration of Gd-DTPA in the SAS increased in a dose-dependent manner following IL-1 beta intracistemal injection. On the other hand, no significant changes in signal intensity of the brain parenchymal areas due to IL-1 beta injection were observed. The findings suggest that the permeability of the BCSFB can be evaluated quantitatively by calculating the GER. MRI with Gd-DTPA provides a useful method to monitor the change in the permeability to the brain barriers. Crown Copyright (C) 2010 Published by Elsevier B.V. All rights reserved.
机构:
Helmholtz Zentrum Munchen, German Res Ctr Environm Hlth, Inst Ecol Chem, D-85764 Neuherberg, GermanyHelmholtz Zentrum Munchen, German Res Ctr Environm Hlth, Inst Ecol Chem, D-85764 Neuherberg, Germany
Nischwitz, Volker
Berthele, Achim
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Tech Univ Munich, Dept Neurol, D-81675 Munich, GermanyHelmholtz Zentrum Munchen, German Res Ctr Environm Hlth, Inst Ecol Chem, D-85764 Neuherberg, Germany
Berthele, Achim
Michalke, Bernhard
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Helmholtz Zentrum Munchen, German Res Ctr Environm Hlth, Inst Ecol Chem, D-85764 Neuherberg, GermanyHelmholtz Zentrum Munchen, German Res Ctr Environm Hlth, Inst Ecol Chem, D-85764 Neuherberg, Germany
机构:
Saitama Med Univ, Dept Neurosurg, Saitama Med Ctr, Kawagoe, Saitama 3508550, JapanSaitama Med Univ, Dept Neurosurg, Saitama Med Ctr, Kawagoe, Saitama 3508550, Japan
Chang, Han Soo
Nagai, Atsushi
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Saitama Med Univ, Dept Neurosurg, Saitama Med Ctr, Kawagoe, Saitama 3508550, JapanSaitama Med Univ, Dept Neurosurg, Saitama Med Ctr, Kawagoe, Saitama 3508550, Japan
Nagai, Atsushi
Oya, Soichi
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Saitama Med Univ, Dept Neurosurg, Saitama Med Ctr, Kawagoe, Saitama 3508550, JapanSaitama Med Univ, Dept Neurosurg, Saitama Med Ctr, Kawagoe, Saitama 3508550, Japan
Oya, Soichi
Matsui, Toru
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Saitama Med Univ, Dept Neurosurg, Saitama Med Ctr, Kawagoe, Saitama 3508550, JapanSaitama Med Univ, Dept Neurosurg, Saitama Med Ctr, Kawagoe, Saitama 3508550, Japan