Sureda F X, Gabriel C, Pubill D, Pallás M, Escubedo E, Camarasa J, Camins A
Facultat de Farmàcia, Nucli Universitari de Pedralbes, Barcelona, 08028, Spain.
Toxicol Appl Pharmacol. 1999 Apr 1;156(1):1-5. doi: 10.1006/taap.1998.8613.
The effects of the lazaroid compound U-83836E on the glutamate-induced production of reactive oxygen species (ROS) were studied in dissociated rat cerebellar granule cells by flow cytometry. U-83836E completely inhibited ROS production with an estimated IC50 value of 21.7 +/- 9.1 nM. However, U-83836E did not inhibit the glutamate-evoked decrease in mitochondrial membrane potential (MMP). Nevertheless, U-83836E (10 nM to 10 microM) prevented cell death induced by 10 mM of glutamate. At concentrations above 10 microM, U-83836E by itself showed slight cytotoxicity, which was significant at a 100 microM concentration. U-83836E (25 to 200 microM) also increased the cytosolic calcium levels in a concentration-dependent manner. Our results indicate that the cytotoxic effects found at micromolar concentrations of U-83836E could be explained by an increase in [Ca2+]i. Finally, since U-83836E did not prevent the MMP decrease evoked by glutamate, it is suggested that antioxidant pharmacotherapy would not be sufficient to block the neurotoxic effects of glutamate.
通过流式细胞术,在离体大鼠小脑颗粒细胞中研究了拉扎罗类化合物U - 83836E对谷氨酸诱导的活性氧(ROS)产生的影响。U - 83836E完全抑制ROS的产生,估计IC50值为21.7±9.1 nM。然而,U - 83836E并不抑制谷氨酸引起的线粒体膜电位(MMP)降低。尽管如此,U - 83836E(10 nM至10 μM)可防止10 mM谷氨酸诱导的细胞死亡。在浓度高于10 μM时,U - 83836E自身显示出轻微的细胞毒性,在100 μM浓度时具有显著性。U - 83836E(25至200 μM)还以浓度依赖性方式增加胞质钙水平。我们的结果表明,在微摩尔浓度的U - 83836E下发现的细胞毒性作用可能由[Ca2+]i的增加来解释。最后,由于U - 83836E不能阻止谷氨酸引起的MMP降低,提示抗氧化药物治疗不足以阻断谷氨酸的神经毒性作用。