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[通过电子显微镜和差示扫描量热法分析细胞毒性脑水肿中水肿液的分布及组成变化]

[Distribution and constitutional changes of edema fluid in cytotoxic brain edema analyzed by electron microscopy and differential scanning calorimetry].

作者信息

Ishiguri H, Kuchiwaki H, Takada S, Itoh J, Nagasaka M, Kageyama N

出版信息

No To Shinkei. 1987 May;39(5):463-70.

PMID:3620217
Abstract

To understand the pathogenesis of brain edema, we studied distribution and constitutional changes of brain-tissue water by morphological and thermoanalytical methods in cytotoxic brain edema induced by 6-aminonicotinamide (6-ANA). Ninety-two Wistar rats were divided into three groups; Group I rats receiving physiological salt solution intraperitoneally served as controls. Group II and III animals were intraperitoneally given 120 mg/kg and 36 mg/kg of 6-ANA respectively. All animals were starved after injection of drugs to exclude differences in water intake. Then they were decapitated at 3, 6, 12, 24, 36 or 48 hours to measure specific gravity (SG) of large brain tissue (1.1-1.5 g), and to evaluate water content (WC) and free water ratio (FWR) of small brain-tissue samples (15-35 mg) taken from the frontal cortex; WC was measured by a drying-weighing method, and FWR was analyzed with a differential scanning calorimeter. Moreover morphological changes of the frontal cortex of the brain were studied in Group II (n = 12) at 3, 6, 12, 24 and 48 hours with an electron microscope. Neurological status of animals administered 6-ANA (Group II and III) deteriorated with time. Morphological studies showed that perivascular astrocytes and astrocytic processes in the cerebral cortex were swollen most remarkably at 48 hours. However neuronal and endothelial cells were almost intact. The FWR of Group I decreased significantly about four per cent (p less than 0.001) after being starved for 48 hours. But the SG and WC of the group showed little change.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

为了解脑水肿的发病机制,我们采用形态学和热分析方法,研究了6-氨基烟酰胺(6-ANA)诱导的细胞毒性脑水肿中脑组织水的分布及组成变化。92只Wistar大鼠分为三组;第一组大鼠腹腔注射生理盐水作为对照。第二组和第三组动物分别腹腔注射120mg/kg和36mg/kg的6-ANA。注射药物后所有动物均禁食,以排除饮水差异。然后在3、6、12、24、36或48小时断头,测量大脑组织(1.1-1.5g)的比重(SG),并评估取自额叶皮质的小脑组织样本(15-35mg)的含水量(WC)和自由水比率(FWR);WC采用干燥称重法测量,FWR用差示扫描量热仪分析。此外,用电子显微镜研究了第二组(n=12)在3、6、12、24和48小时时大脑额叶皮质的形态变化。给予6-ANA的动物(第二组和第三组)的神经状态随时间恶化。形态学研究表明,大脑皮质血管周围星形胶质细胞和星形胶质细胞突起在48小时时肿胀最为明显。然而,神经元和内皮细胞几乎完好无损。第一组禁食48小时后,FWR显著下降约4%(p<0.001)。但该组的SG和WC变化不大。(摘要截短于250字)

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