首页> 外文期刊>Cellular and molecular biology >Synergistic versus antagonistic actions of glutamate and glutathione: the role of excitotoxicity and oxidative stress in neuronal disease.
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Synergistic versus antagonistic actions of glutamate and glutathione: the role of excitotoxicity and oxidative stress in neuronal disease.

机译:谷氨酸和谷胱甘肽的协同作用与拮抗作用:神经毒性中兴奋性毒性和氧化应激的作用。

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摘要

The etiology of various age-related neurological diseases remains unknown. Sporadic forms ofAlzheimer's, Parkinson's and Lou Gehrig's disease have been linked to environmental factors that cause neuronal cell death either by excitotoxicity or by inducing oxidative stress. Our recent studies have demonstrated that various compounds not previously associated with these diseases, i.e. methionine sulfoximine (MSO), originally isolated from 'agenized' flour, and sitosterol glucoside (BSSG), isolated from the seed of the cycad, appear to be neurotoxins, likely acting by excitotoxic mechanisms. For these compounds, the primary excitotoxic effect appears to involve glutamate release followed by NMDA receptor activation. Lactate dehydrogenase assays demonstrate that both compounds cause rapid cell death in vitro. In addition, both compounds appear to alter antioxidant defense mechanisms, acting particularly on levels of reduced glutathione (GSH). In vivo application of MSO has historically been linked to behavioral abnormalities, including seizures, in various species. Our recent experiments have demonstrated that mice fed cycad flour containing sitosterol glucoside have severe behavioral abnormalities of motor and cognitive function, as well as significant levels of neurodegeneration in cortex, hippocampus, spinal cord and other CNS regions measured post mortem. The combined weight of excitotoxic action, in concert to a decline in antioxidant defenses, induced by molecules such as methionine sulfoximine and sitosterol glucoside is hypothesized to be causal to neuronal degeneration in various neurological diseases. Understanding the mechanisms of action of these and functionally related molecules may serve to focus attention on potential neurotoxins present in the human environment. Only once such molecules have been identified, can we begin to design appropriate pharmaceutical strategies to prevent or halt the progression of the age-related neurological diseases.
机译:各种与年龄有关的神经系统疾病的病因仍然未知。阿尔茨海默氏病,帕金森氏病和楼格里格氏病的零星形式与环境因素有关,这些环境因素通过兴奋性中毒或诱导氧化应激而导致神经元细胞死亡。我们最近的研究表明,以前与这些疾病无关的各种化合物,例如蛋氨酸亚砜亚胺(MSO),最初是从“生化”面粉中分离出来的,而谷固醇葡萄糖苷(BSSG)是从苏铁的种子中分离出来的,似乎是神经毒素,可能是通过兴奋毒性机制起作用。对于这些化合物,主要的兴奋性毒性作用似乎涉及谷氨酸的释放,然后是NMDA受体的激活。乳酸脱氢酶测定表明这两种化合物均可在体外引起快速细胞死亡。此外,这两种化合物似乎都可以改变抗氧化防御机制,特别是对还原型谷胱甘肽(GSH)的水平起作用。历史上,MSO的体内应用与各种物种的行为异常(包括癫痫发作)有关。我们最近的实验表明,喂食含有谷固醇葡萄糖苷的苏铁粉的小鼠具有严重的运动和认知功能行为异常,并且在死后测得的皮质,海马,脊髓和其他CNS区域神经退行性变的水平很高。据推测,由蛋氨酸硫代亚砜和谷固醇葡萄糖苷等分子引起的兴奋性毒性作用的总重量与抗氧化防御能力的下降相一致,可能是导致各种神经系统疾病中神经元变性的原因。了解这些与功能相关分子的作用机制可能有助于将注意力集中在人类环境中存在的潜在神经毒素上。只有确定了此类分子后,我们才能开始设计适当的药物策略来预防或阻止与年龄有关的神经系统疾病的进展。

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