增强受损或病变神经细胞中烟酰胺腺嘌呤二核苷酸水平的益处。

Andrew A Pieper, Steven L McKnight
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引用次数: 13

摘要

三个无偏见的研究都指出了烟酰胺腺嘌呤二核苷酸(NAD+)水平的提高对患病或受损神经元的益处。携带三倍基因的小鼠编码NAD+从烟酰胺中回收的最终酶NMNAT,可以保护轴突免受各种损伤。在携带SARM1基因失活突变的果蝇和小鼠中也观察到轴突对沃勒氏变性的保护作用。SARM1基因产物的功能研究揭示了一种酶活性的存在,这种酶活性直接导致NAD+的水解。最后,在活体小鼠中进行的无偏倚药物筛选发现了一种名为P7C3的神经保护化学物质。对P7C3化学物质的生化研究表明,它可以通过激活修复途径中的第一个酶NAMPT来促进烟酰胺对NAD+的回收。综上所述,这三个不相关的研究努力为提高NAD+水平对受损神经元的益处提供了证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Benefits of Enhancing Nicotinamide Adenine Dinucleotide Levels in Damaged or Diseased Nerve Cells.

Three unbiased lines of research have commonly pointed to the benefits of enhanced levels of nicotinamide adenine dinucleotide (NAD+) to diseased or damaged neurons. Mice carrying a triplication of the gene encoding the culminating enzyme in NAD+ salvage from nicotinamide, NMNAT, are protected from a variety of insults to axons. Protection from Wallerian degeneration of axons is also observed in flies and mice bearing inactivating mutations in the SARM1 gene. Functional studies of the SARM1 gene product have revealed the presence of an enzymatic activity directed toward the hydrolysis of NAD+ Finally, an unbiased drug screen performed in living mice led to the discovery of a neuroprotective chemical designated P7C3. Biochemical studies of the P7C3 chemical show that it can enhance recovery of NAD+ from nicotinamide by activating NAMPT, the first enzyme in the salvage pathway. In combination, these three unrelated research endeavors offer evidence of the benefits of enhanced NAD+ levels to damaged neurons.

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