Wolf G, Fischer S, Hass P, Abicht K, Keilhoff G
Institute of Biology, Medical Academy of Magdeburg, F.R.G.
Neuroscience. 1991;43(1):31-4. doi: 10.1016/0306-4522(91)90413-i.
Kainate, an agonist of a unique subclass of glutamate receptors (kainate receptor), was injected intracerebroventricularly in rats to induce convulsive reactions and hippocampal damage in order to model glutamate-mediated brain injury. Rats treated with magnesium sulfate (subcutaneously injected, up to 600 mg/kg) were found to be protected from kainate neurotoxicity depending on the dose and time of application. Results were largely consistent with those obtained previously by using quinolinate as an excitotoxic N-methyl-D-aspartate-receptor agonist. Magnesium is discussed as being a natural and relatively safe therapeutic in cases of glutamate-induced (hypoxic, ischemic, traumatic, or convulsive) disorders of the brain.
海人酸是谷氨酸受体(海人酸受体)独特亚类的激动剂,通过脑室内注射到大鼠体内以诱导惊厥反应和海马损伤,从而模拟谷氨酸介导的脑损伤。结果发现,皮下注射硫酸镁(最高600毫克/千克)治疗的大鼠可免受海人酸神经毒性的影响,这取决于给药剂量和时间。这些结果与先前使用喹啉酸作为兴奋性毒性N-甲基-D-天冬氨酸受体激动剂所获得的结果基本一致。镁被认为是治疗谷氨酸诱导的(缺氧、缺血、创伤或惊厥性)脑疾病的一种天然且相对安全的疗法。