Indole-TEMPO conjugates alleviate ischemia-reperfusion injury via attenuation of oxidative stress and preservation of mitochondrial function

Bioorg Med Chem. 2017 May 1;25(9):2545-2568. doi: 10.1016/j.bmc.2017.03.033. Epub 2017 Mar 19.

Abstract

Mitochondrial oxidative damage contributes to a wide range of pathologies including ischemia/reperfusion injury. Accordingly, protecting mitochondria from oxidative damage should possess therapeutic relevance. In the present study, we have designed and synthesized a series of novel indole-TEMPO conjugates that manifested good anti-inflammatory properties in a murine model of xylene-induced ear edema. We have demonstrated that these compounds can protect cells from simulated ischemia/reperfusion (s-I/R)-induced reactive oxygen species (ROS) overproduction and mitochondrial dysfunction. Furthermore, we have demonstrated that indole-TEMPO conjugates can attenuate organ damage induced in rodents via intestinal I/R injury. We therefore propose that the pharmacological profile and mechanism of action of these indole-TEMPO conjugates involve convergent roles, including the ability to decrease free radical production via lipid peroxidation which couples to an associated decrease in ROS-mediated activation of the inflammatory process. We further hypothesize that the protective effects of indole-TEMPO conjugates partially reside in maintaining optimal mitochondrial function.

Keywords: Anti-inflammation activity; Indole-TEMPO conjugates; Ischemia/reperfusion injury; Mitochondrial function; Oxidative damage.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / administration & dosage
  • Anti-Inflammatory Agents, Non-Steroidal / chemical synthesis
  • Anti-Inflammatory Agents, Non-Steroidal / therapeutic use*
  • Antioxidants / administration & dosage
  • Antioxidants / chemistry
  • Antioxidants / therapeutic use*
  • Aspirin / pharmacology
  • Cyclic N-Oxides / administration & dosage
  • Cyclic N-Oxides / chemical synthesis
  • Cyclic N-Oxides / therapeutic use*
  • Cytochromes c / metabolism
  • Human Umbilical Vein Endothelial Cells
  • Humans
  • Indoles / administration & dosage
  • Indoles / chemical synthesis
  • Indoles / pharmacology
  • Indoles / therapeutic use*
  • Intestine, Small / blood supply
  • Intestine, Small / metabolism
  • Intestine, Small / pathology
  • Lipid Peroxidation / drug effects
  • Male
  • Mice, Inbred ICR
  • Mitochondria / drug effects*
  • Mitochondria / metabolism
  • Molecular Dynamics Simulation
  • Neutrophil Infiltration / drug effects
  • Oxidative Stress / drug effects*
  • Rats, Wistar
  • Reactive Oxygen Species / metabolism
  • Reperfusion Injury / drug therapy*
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Antioxidants
  • Cyclic N-Oxides
  • Indoles
  • Reactive Oxygen Species
  • Tumor Necrosis Factor-alpha
  • Cytochromes c
  • Aspirin