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Biochemical and Molecular Biological Insights into Aluminum Toxicity in Biology and Medicine

机译:生物学和药物铝毒性的生化和分子生物学见解

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It was shown that the rate of excretion of aluminum in the urine was assumed to have a limiting value. Therefore, an excess intake of aluminum indicated that the aluminum content in the body remained high for several days after the absorption of aluminum from the intestine. Accumulation of aluminum in the body has been linked to disease conditions. The toxic effects of aluminum to neuronal cells were examined to show apoptotic cell death via endoplasmic reticulum stress, implicating an influence of aluminum on the gene expression. Also, it was shown that astrocyte-neuron interaction was important in the process of toxic effects in the central nervous system. In addition, renin was the only positively identified up-regulated gene in kidneys determined by DNA sequencing. The up-regulation of renin was confirmed by RT-PCR and Western blotting experiments in the dose dependent treatments and the time course observation in mice. The up-regulation of the renin expression by aluminum is a strong indication of the influence of aluminum on the renin-angiotensin-aldosterone-system, resulting in the induction of essential hypertension.
机译:结果表明,假设尿液中铝排泄速率有限制值。因此,铝的过量摄入表明,在从肠道吸收铝后,体内的铝含量仍然很高。体内铝的积累已与疾病病症有关。研究了铝对神经元细胞的毒性作用,通过内质网胁迫显示凋亡细胞死亡,从而暗示铝对基因表达的影响。此外,表明星形胶质细胞 - 神经元相互作用在中枢神经系统中的毒性作用过程中是重要的。此外,肾素是通过DNA测序测定的肾脏中唯一肯定的上调基因。通过RT-PCR和Western印迹实验证实了肾素的上调,在剂量依赖性处理和小鼠中的时间过程观察中。铝的肾素表达的上调是铝对肾素 - 血管紧张素 - 醛固酮系统的影响的强烈指示,导致诱导原发性高血压。

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