Takizawa S, Fujita H, Ogawa S, Shinohara Y
Department of Neurology, Tokai University School of Medicine, Kanagawa, Japan.
J Cereb Blood Flow Metab. 1996 Sep;16(5):1075-8. doi: 10.1097/00004647-199609000-00033.
We investigated the role of carbon monoxide as a neural modulator of extracellular glutamate concentration in rat hippocampus CA1 in transient forebrain ischemia by using metalloporphyrins, which block the production of carbon monoxide through the inhibition of heme oxygenase (HO) activity. Infusion of 10 and 100 microM zinc protoporphyrin IX, which inhibits nitric oxide synthase activity as well as HO activity, significantly increased glutamate concentration compared with that on the vehicle-treated side. However, infusion of 100 microM tin mesoporphyrin IX, which inhibits only HO activity, did not affect glutamate concentration in ischemia. Our results therefore do not support the hypothesis that carbon monoxide acts as a neural messenger through the modulation of extracellular glutamate concentration in ischemia.
我们通过使用金属卟啉研究了一氧化碳在短暂性前脑缺血大鼠海马CA1区作为细胞外谷氨酸浓度神经调节剂的作用,金属卟啉可通过抑制血红素加氧酶(HO)活性来阻断一氧化碳的产生。输注抑制一氧化氮合酶活性以及HO活性的10微摩尔和100微摩尔原卟啉锌IX,与溶剂处理侧相比,显著增加了谷氨酸浓度。然而,输注仅抑制HO活性的100微摩尔中卟啉锡IX,对缺血时的谷氨酸浓度没有影响。因此,我们的结果不支持一氧化碳通过调节缺血时细胞外谷氨酸浓度作为神经信使的假说。