Antioxidants Protect against Arsenic Induced Mitochondrial Cardio-Toxicity

Clare Pace1, Ruben Dagda2, Jeff Angermann3

  • 1Department of Environmental Science and Health, University of Nevada, Reno, NV 89557, USA. clare.pace@gmail.com.

Toxics
|December 6, 2017
PubMed

Insights

Antioxidants can reverse arsenic-induced cardiovascular damage by protecting mitochondria from oxidative stress. This research identifies 21 antioxidants with potential to improve heart health for those exposed to arsenic.

Area of Science:

  • Cardiovascular Toxicology
  • Mitochondrial Dysfunction
  • Oxidative Stress Research

Background:

  • Arsenic is a known cardiovascular toxicant and carcinogen.
  • Therapeutic arsenic compounds like arsenic trioxide cause severe cardiovascular side effects.
  • Arsenic toxicity is linked to mitochondrial dysfunction and oxidative stress.

Purpose of the Study:

  • To investigate the effectiveness of antioxidants against arsenic-induced cardiovascular dysfunction.
  • To identify antioxidants that can protect cardiovascular cells and tissues from arsenic toxicity.
  • To explore the potential of antioxidants in mitigating cardiovascular risks associated with arsenic exposure.

Main Methods:

  • Literature review identifying antioxidants with mito-protective properties.
  • Analysis of evidence for antioxidant efficacy in reversing mitochondrial dysfunction and oxidative stress.
  • Assessment of antioxidant potential in cardiovascular cells and tissues.

Main Results:

  • Identified 21 antioxidants capable of reversing mitochondrial dysfunction and oxidative stress.
  • Demonstrated that antioxidant phytonutrients can scavenge free radicals, ameliorating arsenic's toxic effects.
  • Highlighted the potential of these antioxidants to improve cardiovascular health in arsenic-exposed populations.

Conclusions:

  • Antioxidants show significant promise in combating arsenic-induced cardiovascular toxicity.
  • Further research is needed to enhance antioxidant bioavailability and targeted delivery for clinical application.
  • Developing novel mito-protective antioxidants could benefit millions exposed to arsenic through environmental or therapeutic sources.

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