Not Just the Brain: Methamphetamine Disrupts Blood-Spinal Cord Barrier and Induces Acute Glial Activation and Structural Damage of Spinal Cord Cells

脊髓 血脑屏障 中枢神经系统 冰毒- 埃文斯蓝 甲基苯丙胺 热疗 胶质纤维酸性蛋白 医学 神经炎症 神经科学 病理 麻醉 药理学 化学 免疫学 内分泌学 内科学 生物 炎症 免疫组织化学 有机化学 聚合物 单体 丙烯酸酯
作者
Eugene A. Kiyatkin,Hari Shanker Sharma
出处
期刊:Cns & Neurological Disorders-drug Targets [Bentham Science]
卷期号:14 (2): 282-294 被引量:17
标识
DOI:10.2174/1871527314666150217121354
摘要

Acute methamphetamine (METH) intoxication induces metabolic brain activation as well as multiple physiological and behavioral responses that could result in life-threatening health complications. Previously, we showed that METH (9 mg/kg) used in freely moving rats induces robust leakage of blood-brain barrier, acute glial activation, vasogenic edema, and structural abnormalities of brain cells. These changes were tightly correlated with drug-induced brain hyperthermia and were greatly potentiated when METH was used at warm ambient temperatures (29°C), inducing more robust and prolonged hyperthermia. Extending this line of research, here we show that METH also strongly increases the permeability of the blood-spinal cord barrier as evidenced by entry of Evans blue and albumin immunoreactivity in T9-12 segments of the spinal cord. Similar to the blood-brain barrier, leakage of bloodspinal cord barrier was associated with acute glial activation, alterations of ionic homeostasis, water tissue accumulation (edema), and structural abnormalities of spinal cord cells. Similar to that in the brain, all neurochemical alterations correlated tightly with drug-induced elevations in brain temperature and they were enhanced when the drug was used at 29°C and brain hyperthermia reached pathological levels (>40°C). We discuss common features and differences in neural responses between the brain and spinal cord, two inseparable parts of the central nervous system affected by METH exposure. Keywords: Albumin leakage, blood-spinal cord barrier, brain, cellular damage, glial fibrillary acidic protein, hyperthermia, metabolic brain activation, spinal cord.

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