Sharma Hari S, Kiyatkin Eugene A
Laboratory of Cerebrovascular Research, Department of Surgical Sciences, University Hospital, Uppsala University, SE-751 85 Uppsala, Sweden.
J Chem Neuroanat. 2009 Jan;37(1):18-32. doi: 10.1016/j.jchemneu.2008.08.002. Epub 2008 Aug 19.
This study describes morphological abnormalities of brain cells during acute methamphetamine (METH) intoxication in the rat and demonstrates the role of hyperthermia, disruption of the blood-brain barrier (BBB) and edema in their development. Rats with chronically implanted brain, muscle and skin temperature probes and an intravenous (i.v.) catheter were exposed to METH (9 mg/kg) at standard (23 degrees C) and warm (29 degrees C) ambient temperatures, allowing for the observation of hyperthermia ranging from mild to pathological (38-42 degrees C). When brain temperature peaked or reached a level suggestive of possible lethality (>41.5 degrees C), rats were injected with Evans blue (EB), rapidly anesthetized, perfused, and their brains were taken for further analyses. Four brain areas (cortex, hippocampus, thalamus and hypothalamus) were analyzed for EB extravasation, water and electrolyte (Na(+), K(+), Cl(-)) contents, immunostained for albumin and glial fibrillary acidic protein (GFAP), and examined for neuronal, glial and axonal alterations using standard light and electron microscopy. These examinations revealed profound abnormalities in neuronal, glial, and endothelial cells, which were stronger with METH administered at 29 degrees C than 23 degrees C and tightly correlated with brain and body hyperthermia. These changes had some structural specificity, but in each structure they tightly correlated with increases in EB levels, the numbers of albumin-positive cells, and water and ion contents, suggesting leakage of the BBB, acutely developing brain edema, and serious shifts in brain ion homeostasis as leading factors underlying brain abnormalities. While most of these acute structural and functional abnormalities appear to be reversible, they could trigger subsequent cellular alterations in the brain and accelerate neurodegeneration-the most dangerous complication of chronic amphetamine-like drug abuse.
本研究描述了大鼠急性甲基苯丙胺(METH)中毒期间脑细胞的形态学异常,并证明了体温过高、血脑屏障(BBB)破坏和水肿在其发展过程中的作用。将长期植入脑、肌肉和皮肤温度探头以及静脉内(i.v.)导管的大鼠在标准(23摄氏度)和温暖(29摄氏度)环境温度下暴露于METH(9毫克/千克),以观察从轻度到病理性(38 - 42摄氏度)的体温过高情况。当脑温达到峰值或达到可能致死的水平(>41.5摄氏度)时,给大鼠注射伊文思蓝(EB),迅速麻醉、灌注,然后取出大脑进行进一步分析。对四个脑区(皮质、海马体、丘脑和下丘脑)分析EB外渗、水和电解质(Na⁺、K⁺、Cl⁻)含量,进行白蛋白和胶质纤维酸性蛋白(GFAP)免疫染色,并使用标准光学和电子显微镜检查神经元、胶质细胞和轴突的改变。这些检查揭示了神经元、胶质细胞和内皮细胞的严重异常,在29摄氏度下给予METH时比在23摄氏度下更严重,并且与脑和身体体温过高密切相关。这些变化具有一定的结构特异性,但在每个结构中它们都与EB水平升高、白蛋白阳性细胞数量以及水和离子含量密切相关,表明血脑屏障渗漏、急性发展的脑水肿以及脑离子稳态的严重改变是脑异常的主要潜在因素。虽然这些急性结构和功能异常中的大多数似乎是可逆的,但它们可能引发大脑随后的细胞改变并加速神经退行性变——慢性苯丙胺类药物滥用最危险的并发症。