Sada Y, Moriki T, Kuwahara S, Yamane T, Hara H
First Department of Pathology, Kochi Medical School, Nankoku, Japan.
Zentralbl Pathol. 1994 Nov;140(4-5):289-98.
The purpose of the present study is to examine the blood-brain barrier in brain of congenital hydrocephalus HTX rats. We investigated the rat brain from postnatal day 1 to 44 using light and electron microscopy and immunohistochemical methods with monoclonal anti-blood-brain barrier (BBB) antibody. HTX rats developed hydrocephalus at 1-2 days after birth. Most rats succumbed to brain changes within 4-5 weeks. Among 136 HTX rats examined, 45 rats succumbed within 1 week after birth, 29 rats between 1-2 weeks, and 4 rats 27-44 days after birth. Out of 88 hydrocephalic rats 54 showed a marked ventricular dilatation, and 34 showed a mild dilatation. Dilatation of lateral ventricles was mild in the rats at 1-2 days after birth, but 3-14-day-old rats showed moderate or marked dilatation. 15-30 days after birth the rats developed mostly marked dilatation of lateral ventricles and third ventricle. Lateral ventricles and third ventricle showed a symmetric dilatation, but ependymal cell layers were well preserved. Aqueduct exhibited no dilatation in any rat. There were spongy appearances and cystic cavities in the white matter around the lateral ventricles. There were glial fibers and capillaries across the cystic cavities. Cystic lesions were also found in the deep subcortical white matter, consisting of spongy changes with extended extracellular spaces and microcysts in the white matter. Immunohistochemically, the anti-BBB reactivity in the normal control rats was at first weak at 2 weeks after birth and increased with the course of development, prominently 4 weeks after birth. Three- and four-week-old HTX rats with hydrocephalus showed moderate positive anti-BBB reaction in the cerebral cortex, the basal ganglia, and around the aqueduct but only a very weak reaction in the deep subcortical white matter and in the subependymal area of lateral ventricles. Laminin immunoreactivity was not different in the capillaries of hydrocephalic brain as compared with normal brain. Electron microscopically, tight junctions were well formed between endothelial cells of capillaries in the subcortical white matter. Occasionally capillaries with partial defect of basal membrane could be found, where the cytoplasm of endothelial cell was protruding between pericytic cytoplasm. Swelling of astrocytic end-feet were found around the microvessels. The results suggest that at the site of the lesion there is underdevelopment or immaturity of the blood-brain barrier.
本研究的目的是检测先天性脑积水HTX大鼠脑内的血脑屏障。我们使用光镜、电镜以及单克隆抗血脑屏障(BBB)抗体免疫组化方法,对出生后1天至44天的大鼠脑进行了研究。HTX大鼠在出生后1 - 2天出现脑积水。大多数大鼠在4 - 5周内死于脑部病变。在检查的136只HTX大鼠中,45只在出生后1周内死亡,29只在1 - 2周内死亡,4只在出生后27 - 44天死亡。在88只脑积水大鼠中,54只表现出明显的脑室扩张,34只表现为轻度扩张。出生后1 - 2天的大鼠侧脑室扩张较轻,但3 - 14日龄的大鼠表现为中度或明显扩张。出生后15 - 30天,大鼠大多出现侧脑室和第三脑室的明显扩张。侧脑室和第三脑室呈对称性扩张,但室管膜细胞层保存完好。导水管在任何大鼠中均未出现扩张。侧脑室周围白质有海绵样外观和囊腔。囊腔内有胶质纤维和毛细血管。在皮质下深部白质也发现了囊性病变,由白质中细胞外间隙扩大和微囊肿形成的海绵样改变组成。免疫组化结果显示,正常对照大鼠的抗BBB反应在出生后2周时起初较弱,随发育进程增强,在出生后4周时显著增强。3周和4周龄患有脑积水的HTX大鼠在大脑皮质、基底神经节和导水管周围显示中度抗BBB阳性反应,但在皮质下深部白质和侧脑室室管膜下区域仅显示非常弱的反应。与正常脑相比,脑积水脑毛细血管中的层粘连蛋白免疫反应性无差异。电镜下,皮质下白质毛细血管内皮细胞之间紧密连接形成良好。偶尔可发现基底膜部分缺损的毛细血管,内皮细胞的细胞质在周细胞细胞质之间突出。在微血管周围发现星形胶质细胞终足肿胀。结果表明,在病变部位存在血脑屏障发育不全或不成熟的情况。