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T-588可保护运动神经元免受谷氨酸诱导的神经毒性作用而死亡。

T-588 protects motor neuron death against glutamate-induced neurotoxicity.

作者信息

Iwasaki Yasuo, Ichikawa Yasumitsu, Igarasi Osamu, Aoyagi Joe, Konno Shingo, Ikeda Ken, Iguchi Hiroaki, Kawabe Seiichi, Marubuchi Shigeki, Ono Satoshi

机构信息

Department of Neurology, Toho University Omori Hospital, Tokyo, Japan.

出版信息

Neurochem Res. 2003 Dec;28(12):1829-32. doi: 10.1023/a:1026167624054.

Abstract

To examine the possible neuroprotective effect of T-588 against glutamate-induced neurotoxicity, we analyzed the pharmacological utility of T-588 in a postnatal organotypic culture model of motor neuron degeneration. Treatment with 10(-5) M of glutamate resulted a motor neuron loss and decreased activity of choline acetyltransferase (ChAT). Cotreatment of 10(-5) M of glutamate and T-588 revealed a protective effect against motor neuron death and decreased ChAT activity. We concluded that T-588 may play important roles in the survival and maintenance of spinal motor neurons in its neuroprotection against glutamate-induced neurotoxicity. Our data may provide a rationale for designing a therapeutic strategy for protection against pathologically induced motor neuron damage or cell death such as amyotrophic lateral sclerosis and motor neuropathy.

摘要

为了研究T - 588对谷氨酸诱导的神经毒性可能的神经保护作用,我们在运动神经元变性的出生后器官型培养模型中分析了T - 588的药理效用。用10(-5)M谷氨酸处理导致运动神经元丢失以及胆碱乙酰转移酶(ChAT)活性降低。10(-5)M谷氨酸与T - 588共同处理显示出对运动神经元死亡的保护作用,并降低了ChAT活性。我们得出结论,T - 588在其对谷氨酸诱导的神经毒性的神经保护作用中,可能在脊髓运动神经元的存活和维持中发挥重要作用。我们的数据可能为设计针对病理性诱导的运动神经元损伤或细胞死亡(如肌萎缩侧索硬化症和运动神经病)的治疗策略提供理论依据。

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