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依布硒啉在氧糖剥夺条件下诱导C6胶质瘤细胞死亡。

Ebselen induced C6 glioma cell death in oxygen and glucose deprivation.

作者信息

Shi Honglian, Liu Shimin, Miyake Minoru, Liu Ke Jian

机构信息

Pharmaceutical Sciences Division, College of Pharmacy, University of New Mexico, Albuquerque, New Mexico, USA.

出版信息

Chem Res Toxicol. 2006 May;19(5):655-60. doi: 10.1021/tx0502544.

Abstract

Studies have shown that ebselen is an antiinflammatory and antioxidative agent. Its protective effect has been investigated in oxidative stress related diseases such as cerebral ischemia in recent years. However, experimental evidence also shows that ebselen causes cell death in several different cell types. Whether ebselen will have a beneficial or detrimental effect on cells under ischemic condition is not known. Herein, we studied the effect of ebselen on C6 glioma cells under oxygen and glucose deprivation (OGD), an in vitro ischemic model. We found that ebselen significantly enhanced cell death after 3 h of OGD as observed by lactase dehydrogenase (LDH) release and cellular morphological changes. Further studies revealed that depletion of cellular glutathione level by the combined action of ebselen and OGD played a role in enhanced cell death as demonstrated by the following evidence: (1) cellular GSH was significantly depleted by the combined effort of ebselen and OGD, compared to that of ebselen or OGD insult alone; (2) exogenous addition of N-acetyl cysteine completely diminished the cell damage induced by ebselen and OGD; (3) supplement of glucose, which provides cellular reducing agents and thus maintains cellular GSH level, to the OGD medium diminished C6 cell damage induced by ebselen. We conclude that depleting cellular glutathione plays an important role in ebselen-induced cell death with OGD. Our results suggest that ebselen can have a beneficial or toxic effect, depending on the availability of GSH.

摘要

研究表明,依布硒啉是一种抗炎和抗氧化剂。近年来,其在氧化应激相关疾病如脑缺血中的保护作用已得到研究。然而,实验证据也表明,依布硒啉会导致几种不同细胞类型的细胞死亡。在缺血条件下,依布硒啉对细胞是产生有益还是有害的影响尚不清楚。在此,我们研究了依布硒啉对氧糖剥夺(OGD)条件下C6胶质瘤细胞的影响,OGD是一种体外缺血模型。我们发现,通过乳酸脱氢酶(LDH)释放和细胞形态变化观察到,依布硒啉在OGD 3小时后显著增强了细胞死亡。进一步研究表明,依布硒啉和OGD的联合作用导致细胞内谷胱甘肽水平降低,在增强细胞死亡中起作用,如下列证据所示:(1)与单独的依布硒啉或OGD损伤相比,依布硒啉和OGD的联合作用显著降低了细胞内谷胱甘肽水平;(2)外源性添加N-乙酰半胱氨酸完全消除了依布硒啉和OGD诱导的细胞损伤;(3)向OGD培养基中补充葡萄糖,葡萄糖可提供细胞还原剂并因此维持细胞内谷胱甘肽水平,减少了依布硒啉诱导 的C6细胞损伤。我们得出结论,细胞内谷胱甘肽的消耗在依布硒啉诱导的OGD细胞死亡中起重要作用。我们的结果表明,依布硒啉可能具有有益或毒性作用,这取决于谷胱甘肽的可用性。

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