Mocchegiani Eugenio
Immunolgy Center, Section of Nutrigenomics and Immunosenenscence, Res. Dept. INRCA, Ancona, Italy.
Rejuvenation Res. 2008 Apr;11(2):419-23. doi: 10.1089/rej.2008.0686.
Aging is characterized by spontaneous biochemical changes that may predispose to increased susceptibility to diseases. Zinc may remodel these changes leading to healthy aging because zinc improves antioxidant defense via CLU protein and genomic stability via PARP-1 nuclear enzyme and repairs oxidized proteins via Msr A protein. The intracellular zinc homeostasis is regulated by metallothioneins (MT), which are unable in zinc release in aging, causing impaired antioxidant response restored by zinc supplementation. Here, the choice of old subjects for zinc supplementation is discussed in relation to their genetic background of MT and IL-6, because both affect intracellular zinc homeostasis.
衰老的特征是自发的生化变化,这可能会增加患病易感性。锌可能重塑这些变化,从而实现健康衰老,因为锌可通过CLU蛋白改善抗氧化防御,通过PARP-1核酶改善基因组稳定性,并通过Msr A蛋白修复氧化蛋白。细胞内锌稳态由金属硫蛋白(MT)调节,MT在衰老过程中无法释放锌,导致抗氧化反应受损,而补充锌可恢复这种反应。在此,结合MT和IL-6的遗传背景讨论了选择老年受试者进行锌补充的问题,因为这两者都会影响细胞内锌稳态。