Ischemic post-conditioning attenuates acute lung injury induced by intestinal ischemia-reperfusion in mice: role of Nrf2

Lab Invest. 2016 Oct;96(10):1087-104. doi: 10.1038/labinvest.2016.87. Epub 2016 Aug 8.

Abstract

Intestinal ischemic post-conditioning (IPo) protects against lung injury induced by intestinal ischemia-reperfusion (IIR) partly through promotion of expression and function of heme oxygenase-1 (HO-1). NF-E2-related factor-2 (Nrf2) is a key transcription factor that interacts with HO-1 and regulates antioxidant defense. However, the role of Nrf2 in IPo protection of IIR-induced pulmonary injury is not completely understood. Here we show that IPo significantly attenuated IIR-induced lung injury and suppressed oxidative stress and systemic inflammatory responses. IPo also increased the expression of both Nrf2 and HO-1. Consistently, the beneficial effects of IPo were abolished by ATRA and Brusatol, potent inhibitors of Nrf2. Moreover, the Nrf2 agonist t-BHQ showed similar activity as IPo. Taken together, our data suggest that Nrf2 activity, along with HO-1, plays an important role in the protective effects of IPo against IIR-induced acute lung injury.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Lung Injury / etiology
  • Acute Lung Injury / metabolism
  • Acute Lung Injury / prevention & control*
  • Animals
  • Glutathione Peroxidase / metabolism
  • Heme Oxygenase-1 / metabolism
  • Interleukin-6 / blood
  • Intestines / blood supply*
  • Ischemic Postconditioning*
  • Lung / enzymology
  • Male
  • Malondialdehyde / metabolism
  • Membrane Proteins / metabolism
  • Mice, Inbred C57BL
  • NF-E2-Related Factor 2 / metabolism*
  • Random Allocation
  • Reperfusion Injury / complications*
  • Superoxide Dismutase / metabolism
  • Tumor Necrosis Factor-alpha / blood

Substances

  • Interleukin-6
  • Membrane Proteins
  • NF-E2-Related Factor 2
  • Nfe2l2 protein, mouse
  • Tumor Necrosis Factor-alpha
  • interleukin-6, mouse
  • Malondialdehyde
  • Glutathione Peroxidase
  • Heme Oxygenase-1
  • Hmox1 protein, mouse
  • Superoxide Dismutase