New Horizons in Diabetic Neuropathy: Mechanisms, Bioenergetics, and Pain

被引:628
作者
Feldman, Eva L. [1 ]
Nave, Klaus-Armin [2 ]
Jensen, Troels S. [3 ,4 ]
Bennett, David L. H. [5 ]
机构
[1] Univ Michigan, Dept Neurol, Ann Arbor, MI 48109 USA
[2] Max Planck Inst Expt Med, Dept Neurogenet, Hermann Rein Str 3, D-37075 Gottingen, Germany
[3] Aarhus Univ, Dept Neurol, DK-8000 Aarhus C, Denmark
[4] Aarhus Univ, Danish Pain Res Ctr, DK-8000 Aarhus C, Denmark
[5] Univ Oxford, Nuffield Dept Clin Neurosci, Oxford OX3 9DU, England
关键词
PROTEIN-KINASE-C; PERIPHERAL NERVOUS-SYSTEM; ALDOSE REDUCTASE INHIBITORS; GENE-EXPRESSION PROFILES; SODIUM-CHANNELS; DOUBLE-BLIND; CLINICAL-MANIFESTATIONS; AUTONOMIC NEUROPATHY; INTENSIVE TREATMENT; INSULIN-RESISTANCE;
D O I
10.1016/j.neuron.2017.02.005
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Pre-diabetes and diabetes are a global epidemic, and the associated neuropathic complications create a substantial burden on both the afflicted patients and society as a whole. Given the enormity of the problem and the lack of effective therapies, there is a pressing need to understand the mechanisms underlying diabetic neuropathy (DN). In this review, we present the structural components of the peripheral nervous system that underlie its susceptibility to metabolic insults and then discuss the pathways that contribute to peripheral nerve injury in DN. We also discuss systems biology insights gleaned from the recent advances in biotechnology and bioinformatics, emerging ideas centered on the axon-Schwann cell relationship and associated bioenergetic crosstalk, and the rapid expansion of our knowledge of the mechanisms contributing to neuropathic pain in diabetes. These recent advances in our understanding of DN pathogenesis are paving the way for critical mechanism-based therapy development.
引用
收藏
页码:1296 / 1313
页数:18
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