Brain damage in neonatal rats following kaolin induction of hydrocephalus

被引:104
作者
Khan, Osaama H.
Enno, Terry L.
Del Bigio, Marc R.
机构
[1] Univ Manitoba, Dept Pathol, Winnipeg, MB R3E 3P5, Canada
[2] Manitoba Inst Child Hlth, Winnipeg, MB, Canada
关键词
axon; white matter injury; cerebral ventricle; myelin; oligodendrocyte; subventricular zone;
D O I
10.1016/j.expneurol.2006.02.113
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Neonatal and congenital hydrocephalus are common problems in humans. Hydrocephalus was induced in 1-day-old rats by injection of kaolin into the cisterna magna. At 7 and 21 days, magnetic resonance (MR) imaging was used to assess ventricle size, then brains were subjected to histopathological and biochemical analyses. Hydrocephalic pups did not exhibit delays in righting or negative geotaxis reflexes during the first week. At 7 days, there was variable ventricular enlargement with periventricular white matter edema, axon damage, reactive astrogliosis, and accumulation of macrophages in severe but not mild hydrocephalus. Cellular proliferation in the subependymal zone was significantly reduced. The cortical subplate neuron layer was disrupted. In rats allowed to survive to 21 days, weight was significantly lower in severely hydrocephalic rats. They also exhibited impaired memory in the Morris water maze test. Despite abnormal posture, there was minimal quantitative impairment of walking ability on a rotating cylinder. At 21 days, histological studies showed reduced corpus callosum thickness, fewer mature oligodendrocytes, damaged axons, and astroglial/microglial reaction. Reduced myelin basic protein, increased glial fibrillary acidic protein, and stable synaptophysin content were demonstrated by immunochemical methods. In conclusion, impairment in cognition and motor skills corresponds to ventricular enlargement and white matter destruction. Quantitative measures of weight, memory, ventricle size, and myelin, and glial proteins in this neonatal model of hydrocephalus will be useful tools for assessment of experimental therapeutic interventions. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:311 / 320
页数:10
相关论文
共 54 条
[1]   POSTNATAL-DEVELOPMENT OF LOCOMOTION IN LABORATORY RAT [J].
ALTMAN, J ;
SUDARSHAN, K .
ANIMAL BEHAVIOUR, 1975, 23 (NOV) :896-920
[2]   Persistent motor deficit following infusion of autologous blood into the periventricular region of neonatal rats [J].
Balasubramaniam, J ;
Xue, MZ ;
Buist, RJ ;
Ivanco, TL ;
Natutik, S ;
Del Bigio, MR .
EXPERIMENTAL NEUROLOGY, 2006, 197 (01) :122-132
[3]   2′3′cyclic nucleotide 3′phosphodiesterase immunohistochemistry shows an impairment on myelin compaction in hypothyroid rats [J].
Barradas, PC ;
Ferraz, AS ;
Ferreira, AA ;
Daumas, RP ;
Moura, EG .
INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE, 2000, 18 (08) :887-892
[4]  
Bayer SA, 1995, PEDIAT NEUROPATHOLOG, P54
[5]   Ultrastructural changes in the deep cortical pyramidal cells of infant rats with inherited hydrocephalus and the effect of shunt treatment [J].
Boillat, CA ;
Jones, HC ;
Kaiser, GL ;
Harris, NG .
EXPERIMENTAL NEUROLOGY, 1997, 147 (02) :377-388
[6]   HEREDITARY HYDROCEPHALUS IN LABORATORY-ANIMALS AND HUMANS [J].
BRUNI, JE ;
DELBIGIO, MR ;
CARDOSO, ER ;
PERSAUD, TVN .
EXPERIMENTAL PATHOLOGY, 1988, 35 (04) :239-246
[7]  
Castejon O. J., 2001, Journal of Submicroscopic Cytology and Pathology, V33, P33
[8]   Posthemorrhagic ventricular dilation in the neonate: Development and characterization of a rat model [J].
Cherian, SS ;
Love, S ;
Silver, IA ;
Porter, HJ ;
Whitelaw, AGL ;
Thoresen, M .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2003, 62 (03) :292-303
[9]   MONOAMINE ALTERATIONS DURING EXPERIMENTAL HYDROCEPHALUS IN NEONATAL RATS [J].
CHOVANES, GI ;
MCALLISTER, JP ;
LAMPERTI, AA ;
SALOTTO, AG ;
TRUEX, RC .
NEUROSURGERY, 1988, 22 (01) :86-91
[10]   Progressive ventricular enlargement in the absence of high ventricular pressure in an experimental neonatal rat model [J].
Cosan, TE ;
Guner, AI ;
Akcar, N ;
Uzuner, K ;
Tel, E .
CHILDS NERVOUS SYSTEM, 2002, 18 (1-2) :10-14