矿物质代谢和衰老。

Makoto Kuro-O
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引用次数: 0

摘要

对表现出加速衰老的突变小鼠的分析表明,磷在哺乳动物中是一种促进衰老的因素。在血液中,磷以磷酸盐离子和固相磷酸钙与血清蛋白fetuin-A组成的胶体颗粒的形式存在,称为钙蛋白颗粒(calprotein particles, CPP)。血CPP水平随年龄和肾功能下降而升高。由于CPP在体外具有诱导炎症和血管平滑肌细胞钙化的能力,我们假设CPP可能作为加速衰老的病原体。磷酸盐和/或CPP的治疗干预可能为实际抗衰老药物开辟新的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Mineral metabolism and aging.]

Analysis of a mutant mouse exhibiting accelerated aging identified phosphorus as a pro-aging factor in mammals. In the blood, phosphorus exists in the form of phosphate ions and colloidal particles composed of solid-phase calcium-phosphate and serum protein fetuin-A, which are termed calciprotein particles(CPP). Blood CPP levels increase with age and decline of renal function. Because CPP have the ability to induce inflammation and vascular smooth muscle cell calcification in vitro, we hypothesize that CPP may serve as a pathogen that accelerates aging. Therapeutic interventions in phosphate and/or CPP may open a new avenue for practical anti-aging medicine.

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