Adams James D
School of Pharmacy, University of Southern California, Los Angeles, CA 90089-9121, USA.
CNS Neurol Disord Drug Targets. 2008 Dec;7(6):492-8. doi: 10.2174/187152708787122969.
This review discusses new mechanisms for the induction of Alzheimer's disease, involving lipid toxicity and adipokines. Ceramide induces oxidative stress and the formation of amyloid beta. Visfatin induces oxidative stress, damages the blood brain barrier and increases the attraction of monocytes, neutrophils and other white blood cells. A new mechanism for visfatin/NAD (nicotinamide adenine dinucleotide)-induced oxidative stress is presented involving redox cycling catalyzed by xanthine dehydrogenase and NADH oxidase. These mechanisms are discussed in terms of the treatment of Alzheimer's disease.
本综述讨论了阿尔茨海默病诱导的新机制,涉及脂质毒性和脂肪因子。神经酰胺诱导氧化应激和β-淀粉样蛋白的形成。内脂素诱导氧化应激,破坏血脑屏障,并增加单核细胞、中性粒细胞和其他白细胞的趋化作用。本文提出了一种内脂素/烟酰胺腺嘌呤二核苷酸(NAD)诱导氧化应激的新机制,该机制涉及由黄嘌呤脱氢酶和NADH氧化酶催化的氧化还原循环。从阿尔茨海默病的治疗角度对这些机制进行了讨论。