Quantitative evaluation of blood-cerebrospinal fluid barrier permeability in the rat with experimental meningitis using magnetic resonance imaging

被引:9
作者
Ichikawa, Hiroyuki [1 ]
Ishikawa, Makoto [1 ]
Fukunaga, Mari [1 ]
Ishikawa, Koichi [2 ]
Ishiyama, Hironobu [1 ]
机构
[1] Otsuka Pharmaceut Co Ltd, Inst New Drug Discovery 3, Kawaguchi, Tokushima 7710192, Japan
[2] Gunma Univ, Inst Mol & Cellular Regulat, Maebashi, Gunma 3718512, Japan
关键词
Blood-cerebrospinal fluid barrier; Permeability; Magnetic resonance imaging; BRAIN-BARRIER; NITRIC-OXIDE; PATHOPHYSIOLOGY; DISRUPTION; MORTALITY; INJURY; DAMAGE;
D O I
10.1016/j.brainres.2010.01.050
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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.
引用
收藏
页码:125 / 132
页数:8
相关论文
共 29 条
[1]   Age-related effects of interleukin-1 beta on polymorphonuclear neutrophil-dependent increases in blood-brain barrier permeability in rats [J].
Anthony, DC ;
Bolton, SJ ;
Fearn, S ;
Perry, VH .
BRAIN, 1997, 120 :435-444
[2]  
Blamire AM, 2000, J NEUROSCI, V20, P8153
[3]  
BOJE KMK, 1995, J PHARMACOL EXP THER, V274, P1199
[4]   Neuroinflammatory role of prostaglandins during experimental meningitis: Evidence suggestive of an in vivo relationship between nitric oxide and prostaglandins [J].
Boje, KMK ;
Jaworowicz, D ;
Raybon, JJ .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2003, 304 (01) :319-325
[5]   MAGNETIC-RESONANCE-IMAGING CONTRAST AGENTS - THEORY AND APPLICATION TO THE CENTRAL-NERVOUS-SYSTEM [J].
BRONEN, RA ;
SZE, G .
JOURNAL OF NEUROSURGERY, 1990, 73 (06) :820-839
[6]   COMPARATIVE PHARMACOKINETICS OF GADOLINIUM DTPA AND GADOLINIUM CHLORIDE [J].
DEAN, PB ;
NIEMI, P ;
KIVISAARI, L ;
KORMANO, M .
INVESTIGATIVE RADIOLOGY, 1988, 23 :S258-S260
[7]   TRANSIENT BLOOD-BRAIN BARRIER PERMEABILITY FOLLOWING PROFOUND TEMPORARY GLOBAL-ISCHEMIA - AN EXPERIMENTAL-STUDY USING C-14 AIB [J].
DOBBIN, J ;
CROCKARD, HA ;
ROSSRUSSELL, R .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1989, 9 (01) :71-78
[8]   Prevention of brain injury by the nonbacteriolytic antibiotic daptomycin in experimental pneumococcal meningitis [J].
Grandgirard, Denis ;
Schuerch, Christian ;
Cottagnoud, Philippe ;
Leib, Stephen L. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2007, 51 (06) :2173-2178
[9]   Pre-ischemic exercise reduces matrix metalloproteinase-9 expression and ameliorates blood-brain barrier dysfunction in stroke [J].
Guo, M. ;
Cox, B. ;
Mahale, S. ;
Davis, W. ;
Carranza, A. ;
Hayes, K. ;
Sprague, S. ;
Jimenez, D. ;
Ding, Y. .
NEUROSCIENCE, 2008, 151 (02) :340-351
[10]  
IdanpaanHeikkila I, 1997, J INFECT DIS, V176, P704