| Literature DB >> 22548617 |
Lucy M Hinder1, Andrea M Vincent, Charles F Burant, Subramaniam Pennathur, Eva L Feldman.
Abstract
Progress in developing treatments for diabetic neuropathy is slowed by our limited understanding of how disturbances in metabolic substrates - glucose and fatty acids - produce nerve injury. In this review, we present the current oxidative stress hypothesis and experimental data that support it. We identify weaknesses in our understanding of diabetes-disordered metabolism in the neurovascular unit, that is, in critical cell types of the microvascular endothelium, peripheral sensory neurons, and supporting Schwann cells. Greater understanding of peripheral nervous system bioenergetics may provide insight into new drug therapies or improvements in dietary interventions in diabetes or even pre-diabetes.Entities:
Mesh:
Year: 2012 PMID: 22548617 PMCID: PMC3589977 DOI: 10.1111/j.1529-8027.2012.00389.x
Source DB: PubMed Journal: J Peripher Nerv Syst ISSN: 1085-9489 Impact factor: 3.494