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Aluminofluoride Complexes: Phosphate Analogues and a Hidden Hazard for Living Organisms

机译:氟化铝络合物:磷酸盐类似物和对生物体的隐藏危害

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There is a burgeoning body of evidence that aluminum can be implicated as an etiological factor of several neuropathological events. The molecular mechanisms underlying aluminum toxicity are still poorly understood. Reflecting on many studies, we suggest a new view on the toxicity of aluminum in a link with fluoride. Soluble aluminofluoride complexes - fluoroaluminate (AlF_(x)) are formed in water solutions containing fluoride and traces of aluminum. These complexes are able to simulate phosphate groups in many biochemical reactions. AlF_(x) are used in many laboratory investigations of guanine nucleotide binding proteins (G proteins). They affect various enzyme activities and cell signaling cascades. The hidden danger of a long-term synergistic action of aluminum and fluoride is not fully recognized at this point. We suggest that aluminum and fluoride can exacerbate the pathological and clinical problems, namely by interfering with a great number of G-protein-dependent cellular mechanisms, and by worsening excitotoxicity, microglial priming, and brain inflammation. Our suggestion opens the door to a better understanding of mechanisms of aluminum harmful effects on human health.
机译:新兴的证据表明铝可能与多种神经病理学事件的病因有关。铝毒性的分子机制仍知之甚少。通过对许多研究的反思,我们提出了关于铝与氟化物的毒性的新观点。可溶性氟化铝络合物-氟铝酸盐(AlF_(x))在含有氟化物和微量铝的水溶液中形成。这些配合物能够在许多生化反应中模拟磷酸酯基团。 AlF_(x)用于鸟嘌呤核苷酸结合蛋白(G蛋白)的许多实验室研究中。它们影响各种酶活性和细胞信号转导级联。在这一点上,铝和氟化物长期协同作用的潜在危险尚未得到充分认识。我们建议铝和氟化物会加剧病理和临床问题,即干扰大量依赖G蛋白的细胞机制,并加剧兴奋性毒性,小胶质细胞引发和脑部炎症。我们的建议为更好地了解铝对人体健康的有害影响机制打开了大门。

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