Ghribi O, Callebert J, Plotkine M, Boulu R G
Laboratoire de Pharmacologie, Faculté des Sciences Pharmaceutiques et Biologiques, Paris, France.
Neuroreport. 1994 Jan 12;5(4):435-7. doi: 10.1097/00001756-199401120-00016.
We examined the effect of kynurenic acid, a broad spectrum antagonist of excitatory amino acid receptors, on striatal extracellular glutamate and aspartate accumulation induced by a 30 min forebrain ischaemia in rats. Kynurenic acid, given systemically (500 mg kg-1, i.p.) or administered in situ through the dialysis probe (10 mM), markedly depressed the ischaemia-induced increase in glutamate and aspartate concentrations. These results indicate that, during forebrain ischaemia, local glutamate receptors play a major role in glutamate and aspartate accumulation in the striatum. Ischaemia-induced increase in extracellular concentrations of these excitatory amino acids may be due in part to a positive glutamatergic feedback loop via activation of NMDA and/or non-NMDA receptors.
我们研究了犬尿喹啉酸(一种兴奋性氨基酸受体的广谱拮抗剂)对大鼠前脑缺血30分钟所诱导的纹状体细胞外谷氨酸和天冬氨酸蓄积的影响。全身给予犬尿喹啉酸(500毫克/千克,腹腔注射)或通过透析探针原位给予(10毫摩尔),均能显著抑制缺血诱导的谷氨酸和天冬氨酸浓度升高。这些结果表明,在前脑缺血期间,局部谷氨酸受体在纹状体谷氨酸和天冬氨酸蓄积中起主要作用。缺血诱导的这些兴奋性氨基酸细胞外浓度升高可能部分归因于通过NMDA和/或非NMDA受体激活产生的谷氨酸能正反馈回路。