Dimethyl fumarate accelerates wound healing under diabetic conditions. (November 2018)

• Record Type: Journal Article
• Authors: Li, Ying; Ma, Fuzhe; Li, Huimin; Song, Yuguo; Zhang, Huan; Jiang, Ziping; Wu, Hao
• Is Part Of: Journal of molecular endocrinology. Volume 61:Number 4(2018)
• Page Start: 163
• Page End: 172
• Publication Date: 2018-11
• Subjects: diabetes -- keratinocyte -- NRF2 -- oxidative stress -- ROS -- wound healing; Molecular endocrinology -- Periodicals; Endocrinology -- Periodicals; 616.407
• DOI: 10.1530/JME-18-0102
• Languages: English
• ISSNs: 0952-5041

Abstract

Abstract : Impaired wound healing is a common complication among patients with diabetes mellitus (DM), resulting in high rates of disability and mortality. Recent findings highlighted the critical role of nuclear factor erythroid 2-related factor 2 (NRF2) – a master of cellular antioxidants scavenging excessive DM-induced free radicals – in accelerating diabetic wound healing. Dimethyl fumarate (DMF) is a potent NRF2 activator used for the treatment of multiple sclerosis. However, the effect of DMF on wound healing has not been determined. The present study investigated the effect of DMF on the diabetic and the non-diabetic wound healing in streptozotocin-induced diabetic mice and non-diabetic control mice. DMF activated NRF2 signaling under both conditions. Interestingly, DMF attenuated oxidative damage and inflammation and accelerated wound closure in diabetic mice. However, this effect was not observed in non-diabetic mice. Keratinocytes were treated with normal glucose (NG), high glucose (HG) or hydrogen peroxide (H2 O2 ), in the presence or absence of DMF to assess the role of reactive oxygen species (ROS) – inducible in DM – in mediating DMF-induced protection. Both HG and H2 O2 elevated ROS, oxidative damage and inflammation, the effects of which were similarly blunted by DMF. However, in spite of the activation of NRF2, DMF lost this capability under the NG condition. The findings of this study demonstrate that ROS activate the protective effect of DMF on the diabetic wound healing.