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Sci Rep. 2019 Jan 29;9(1):881. doi: 10.1038/s41598-018-37376-y.

Mitochondrial uncoupling has no effect on microvascular complications in type 2 diabetes.

Author information

1
Department of Neurology, University of Michigan, Ann Arbor, MI, 48109, USA.
2
Division of Nephrology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI, 48109, USA.
3
Department of Ophthalmology and Visual Sciences, University of Michigan, Ann Arbor, MI, 48105, USA.
4
Departments of Molecular and Integrative Physiology, University of Michigan, Ann Arbor, MI, 48109, USA.
5
Department of Neurology, University of Michigan, Ann Arbor, MI, 48109, USA. efeldman@umich.edu.

Abstract

Diabetic peripheral neuropathy (DPN), diabetic kidney disease (DKD), and diabetic retinopathy (DR) contribute to significant morbidity and mortality in diabetes patients. The incidence of these complications is increasing with the diabetes epidemic, and current therapies minimally impact their pathogenesis in type 2 diabetes (T2D). Improved mechanistic understanding of each of the diabetic complications is needed in order to develop disease-modifying treatments for patients. We recently identified fundamental differences in mitochondrial responses of peripheral nerve, kidney, and retinal tissues to T2D in BKS-db/db mice. However, whether these mitochondrial adaptations are the cause or consequence of tissue dysfunction remains unclear. In the current study BKS-db/db mice were treated with the mitochondrial uncoupler, niclosamide ethanolamine (NEN), to determine the effects of mitochondrial uncoupling therapy on T2D, and the pathogenesis of DPN, DKD and DR. Here we report that NEN treatment from 6-24 wk of age had little effect on the development of T2D and diabetic complications. Our data suggest that globally targeting mitochondria with an uncoupling agent is unlikely to provide therapeutic benefit for DPN, DKD, or DR in T2D. These data also highlight the need for further insights into the role of tissue-specific metabolic reprogramming in the pathogenesis of diabetic complications.

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