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Potential drugs which activate nuclear factor E2-related factor 2 signaling to prevent diabetic cardiovascular complications: A focus on fumaric acid esters. | LitMetric

AI Article Synopsis

  • Diabetes poses significant public health challenges, particularly due to cardiovascular complications linked to an imbalance of free radicals and antioxidants.
  • Nrf2 is a key transcription factor that enhances the production of antioxidant enzymes and protects against oxidative stress, making it a potential target for preventing complications in diabetic patients.
  • While animal studies suggest that Nrf2 activators could help prevent these complications, human applications are limited due to concerns about safety and efficacy; the review highlights certain clinically-used drugs that up-regulate Nrf2, focusing on dimethyl fumarate and its similar compounds.

Article Abstract

Diabetes and its cardiovascular complications have been a major public health issue. These complications are mainly attributable to a severe imbalance between free radical and reactive oxygen species production and the antioxidant defense systems. Nuclear factor E2-related factor 2 (Nrf2) is a transcription factor that controls the basal and inducible expression of a battery of antioxidant enzyme genes and other cyto-protective phase II detoxifying enzymes. As a result, Nrf2 has gained great attention as a promising drug target for preventing diabetic cardiovascular complications. And while animal studies have shown that several Nrf2 activators manifest a potential to efficiently prevent the diabetic complications, their use in humans has not been approved due to the lack of substantial evidence regarding safety and efficacy of the Nrf2 activation. We provide here a brief review of a few clinically-used drugs that can up-regulate Nrf2 with the potential of extending their usage to diabetic patients for the prevention of cardiovascular complications and conclude with a closer inspection of dimethyl fumarate and its mimic members.

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Source
http://dx.doi.org/10.1016/j.lfs.2015.05.015DOI Listing

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