Mechanisms of high glucose-induced apoptosis and its relationship to diabetic complications

被引:221
作者
Allen, DA [1 ]
Yaqoob, MM [1 ]
Harwood, SM [1 ]
机构
[1] Univ London, John Vane Sci Ctr, Ctr Expt Med Nephrol & Crit Care, William Harvey Res Inst,St Bartholomews & Royal, London EC1M 6BQ, England
关键词
high glucose-induced apoptosis; diabetic complications; mitogen-activated protein kinases; cell-cycle regulators;
D O I
10.1016/j.jnutbio.2005.06.007
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
Cellular responses to high glucose are numerous and varied but ultimately result in functional changes and, often, cell death. High glucose induces oxidative and nitrosative stress in many cell types causing the generation of species such as superoxide, nitric oxide and peroxynitrite and their derivatives. The role of these species in high glucose-mediated apoptotic cell death is relevant to the complications of diabetes such as neuropathy, nephropathy and cardiovascular disease. High glucose causes activation of several proteins involved in apoptotic cell death, including members of the caspase and Bcl-2 families. These events and the relationship between high glucose-induced oxidative stress and apoptosis are discussed here with reference to additional regulators of apoptosis such as the mitogen-activated protein kinases (MAPKs) and cell-cycle regulators. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:705 / 713
页数:9
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