The NAD ratio redox paradox: why does too much reductive power cause oxidative stress?

被引:53
作者
Teodoro, Joao Soeiro [1 ]
Rolo, Anabela Pinto [1 ,2 ]
Palmeira, Carlos Marques [1 ]
机构
[1] Univ Coimbra, Dept Life Sci, Ctr Neurosci & Cell Biol, Coimbra, Portugal
[2] Univ Aveiro, Dept Biol, P-3800 Aveiro, Portugal
关键词
Diabetes; glucose; mitochondria; NADH; NADPH; oxidative stress; ACTIVATED PROTEIN-KINASE; DEPENDENT DIABETIC-PATIENTS; SKELETAL-MUSCLE; MITOCHONDRIAL BIOGENESIS; SORBITOL DEHYDROGENASE; HYPERGLYCEMIC DAMAGE; INSULIN-RESISTANCE; GLUCOSE-TOLERANCE; ALDOSE REDUCTASE; ADIPOSE-TISSUE;
D O I
10.3109/15376516.2012.759305
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
The reductive power provided by nicotinamide adenine dinucleotides is invaluable for several cellular processes. It drives metabolic reactions, enzymatic activity, regulates genetic expression and allows for the maintenance of a normal cell redox status. Therefore, the balance between the oxidized (NAD(+)) and the reduced (NADH) forms is critical for the cell's proper function and ultimately, for its survival. Being intimately associated with the cells' metabolism, it is expected that alterations to the NAD(+)/NADH ratio are to be found in situations of metabolic diseases, as is the case of diabetes. NAD(+) is a necessary cofactor for several enzymes' activity, many of which are related to metabolism. Therefore, a decrease in the NAD(+)/NADH ratio causes these enzymes to decrease in activity (reductive stress), resulting in an altered metabolic situation that might be the first insult toward several pathologies, such as diabetes. Here, we review the importance of nicotinamide adenine dinucleotides in the liver cell and its fluctuations in a state of type 2 diabetes mellitus.
引用
收藏
页码:297 / 302
页数:6
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