Redox imbalance stress in diabetes mellitus: Role of the polyol pathway

被引:186
作者
Yan, Liang-jun [1 ]
机构
[1] Univ North Texas, Hlth Sci Ctr, UNT Syst Coll Pharm, Dept Pharmaceut Sci, Ft Worth, TX 76107 USA
基金
美国国家卫生研究院;
关键词
diabetes mellitus; fructose; NADH/NAD(+); oxidative stress; polyol pathway; redox imbalance stress;
D O I
10.1002/ame2.12001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In diabetes mellitus, the polyol pathway is highly active and consumes approximately 30% glucose in the body. This pathway contains 2 reactions catalyzed by aldose reductase (AR) and sorbitol dehydrogenase, respectively. AR reduces glucose to sorbitol at the expense of NADPH, while sorbitol dehydrogenase converts sorbitol to fructose at the expense of NAD(+), leading to NADH production. Consumption of NADPH, accumulation of sorbitol, and generation of fructose and NADH have all been implicated in the pathogenesis of diabetes and its complications. In this review, the roles of this pathway in NADH/NAD(+) redox imbalance stress and oxidative stress in diabetes are highlighted. A potential intervention using nicotinamide riboside to restore redox balance as an approach to fighting diabetes is also discussed.
引用
收藏
页码:7 / 13
页数:7
相关论文
共 123 条
[71]   Roles of Pyruvate, NADH, and Mitochondrial Complex I in Redox Balance and Imbalance in β Cell Function and Dysfunction [J].
Luo, Xiaoting ;
Li, Rongrong ;
Yan, Liang-Jun .
JOURNAL OF DIABETES RESEARCH, 2015, 2015
[72]  
Lyons TJ, 1997, DIABETES REV, V5, P365
[73]   Targeting Aldose Reductase for the Treatment of Diabetes Complications and Inflammatory Diseases: New Insights and Future Directions [J].
Maccari, Rosanna ;
Ottana, Rosaria .
JOURNAL OF MEDICINAL CHEMISTRY, 2015, 58 (05) :2047-2067
[74]   Investigating the Sensitivity of NAD+-dependent Sirtuin Deacylation Activities to NADH [J].
Madsen, Andreas S. ;
Andersen, Christian ;
Daoud, Mohammad ;
Anderson, Kristin A. ;
Laursen, Jonas S. ;
Chakladar, Saswati ;
Huynh, Frank K. ;
Colaco, Ana R. ;
Backos, Donald S. ;
Fristrup, Peter ;
Hirschey, Matthew D. ;
Olsen, Christian A. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2016, 291 (13) :7128-7141
[75]   Damaging effects of hyperglycemia on cardiovascular function: spotlight on glucose metabolic pathways [J].
Mapanga, Rudo F. ;
Essop, M. Faadiel .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2016, 310 (02) :H153-H173
[76]   Poly(ADP-ribose) polymerase gene disruption conferred mice resistant to streptozotocin-induced diabetes [J].
Masutani, M ;
Suzuki, H ;
Kamada, N ;
Watanabe, M ;
Ueda, O ;
Nozaki, T ;
Jishage, K ;
Watanabe, T ;
Sugimoto, T ;
Nakagama, H ;
Ochiya, T ;
Sugimura, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (05) :2301-2304
[77]   OXIDATIVE INHIBITION OF RED-BLOOD-CELL ATPASES BY GLYCERALDEHYDE [J].
MIRA, ML ;
MARTINHO, F ;
AZEVEDO, MS ;
MANSO, CF .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1060 (03) :257-261
[78]   Seven sirtuins for seven deadly diseases of aging [J].
Morris, Brian J. .
FREE RADICAL BIOLOGY AND MEDICINE, 2013, 56 :133-171
[79]   The structure of human ADP-ribosylhydrolase 3 (ARH3) provides insights into the reversibility of protein ADP-ribosylation [J].
Mueller-Dieckmann, Christoph ;
Kernstock, Stefan ;
Lisurek, Michael ;
von Kriest, Jens Peter ;
Haag, Friedrich ;
Weiss, Manfred S. ;
Koch-Nolte, Friedrich .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (41) :15026-15031
[80]   How mitochondria produce reactive oxygen species [J].
Murphy, Michael P. .
BIOCHEMICAL JOURNAL, 2009, 417 :1-13