Shuaib A, Ijaz M S, Waqar T, Voll C, Kanthan R, Miyashita H, Liu L
Saskatchewan Stroke Research Centre, College of Medicine, University of Saskatchewan, Saskatoon, Canada.
Neuroscience. 1995 Aug;67(4):809-14. doi: 10.1016/0306-4522(95)00093-x.
There are reports that insulin may protect neurons from the effects of ischemia. The mechanisms for this protection are not fully understood. We studied the extracellular levels of glutamate and GABA in insulin-treated animals exposed to transient forebrain ischemia under normoglycemic and hypoglycemic conditions. In vivo microdialysis technique was used to collect extracellular fluid from the CA1 region of the hippocampus. There was a significant increase in GABA levels in the two insulin-treated sub-groups compared with the controls. GABA levels were < 1 pmol/10 microliters in three 10 min collections prior to ischemia in all the groups. It increased from 11.1 +/- 3.5 pmol/10 microliters in the conrol group to 47 +/- 5 (P < 0.001) in the insulin-treated hypoglycemic group and up to 47.2 +/- 9.3+ (P < 0.005) in the insulin-treated normoglycemic group (two-way ANOVA with repeated measures). Ischemia resulted in an increase in the glutamate levels. The glutamate levels returned to baseline within 30 min of the insult. There were no significant differences in the glutamate levels in three groups. The increase in GABA concentrations in the extracellular space may result in the inhibition of CA1 pyramidal neurons. This may be a possible mechanism of neuronal protection in animals treated with insulin (with or without being hypoglycemic) during ischemia.
有报道称胰岛素可能保护神经元免受缺血影响。这种保护机制尚未完全明确。我们研究了在正常血糖和低血糖条件下,暴露于短暂性前脑缺血的胰岛素治疗动物的细胞外谷氨酸和γ-氨基丁酸(GABA)水平。采用体内微透析技术从海马体CA1区收集细胞外液。与对照组相比,两个胰岛素治疗亚组的GABA水平显著升高。所有组在缺血前的三次10分钟采集样本中,GABA水平均<1 pmol/10微升。对照组从11.1±3.5 pmol/10微升升至胰岛素治疗低血糖组的47±5(P<0.001),胰岛素治疗正常血糖组则高达47.2±9.3+(P<0.005)(重复测量的双向方差分析)。缺血导致谷氨酸水平升高。谷氨酸水平在损伤后30分钟内恢复至基线。三组的谷氨酸水平无显著差异。细胞外空间GABA浓度的升高可能导致CA1锥体神经元受到抑制。这可能是缺血期间接受胰岛素治疗(无论是否低血糖)的动物神经元保护的一种可能机制。