Dexmedetomidine postconditioning attenuates myocardial ischemia/reperfusion injury by activating the Nrf2/Sirt3/SOD2 signaling pathway in the rats

Redox Rep. 2023 Dec;28(1):2158526. doi: 10.1080/13510002.2022.2158526.

Abstract

Objectives: To observe the protective effects of dexmedetomidine (Dex) postconditioning on myocardial ischemia/reperfusion injury (IRI) and to explore its potential molecular mechanisms.

Methods: One-hundred forty-seven male Sprague-Dawley rats were randomly divided into five groups receiving the different treatments: Sham, ischemia/reperfusion (I/R), Dex, Brusatol, Dex + Brusatol. By the in vivo rat model of myocardial IRI, cardioprotective effects of Dex postconditioning were evaluated by assessing serum CK-MB and cTnI levels, myocardial HE and Tunel staining and infarct size. Furthermore, the oxidative stress-related markers including intracellular ROS level, myocardial tissue MDA level, SOD and GSH-PX activities were determined.

Results: Dex postconditioning significantly alleviated myocardial IRI, decreased intracellular ROS and myocardial tissue MDA level, increased SOD and GSH-PX activities. Dex postconditioning significantly up-regulated myocardial expression of Bcl-2, down-regulated Bax and cleaved caspase-3 and decreased cardiomyocyte apoptosis rate. furthermores, Dex postconditioning promoted Nrf2 nuclear translocation, increased myocardial expression of Sirt3 and SOD2 and decreased Ac-SOD2. However, brusatol reversed cardioprotective benefits of Dex postconditioning, significantly decreased Dex-induced Nrf2 nuclear translocation and reduced myocardial expression of Sirt3 and SOD2.

Conclusions: Dex postconditioning can alleviate myocardial IRI by suppressing oxidative stress and apoptosis, and these beneficial effects are at least partly mediated by activating the Nrf2/Sirt3/SOD2 signaling pathway.

Keywords: Dexmedetomidine; Nrf2/Sirt3/SOD2 signaling pathway; apoptosis; myocardial ischemia/reperfusion injury; oxidative stress.

MeSH terms

  • Animals
  • Apoptosis
  • Dexmedetomidine* / pharmacology
  • Dexmedetomidine* / therapeutic use
  • Male
  • Myocardial Reperfusion Injury* / drug therapy
  • Myocardial Reperfusion Injury* / metabolism
  • NF-E2-Related Factor 2 / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Reactive Oxygen Species
  • Reperfusion Injury*
  • Signal Transduction
  • Sirtuin 3* / metabolism
  • Sirtuin 3* / pharmacology
  • Superoxide Dismutase / metabolism

Substances

  • brusatol
  • Dexmedetomidine
  • NF-E2-Related Factor 2
  • Reactive Oxygen Species
  • Sirtuin 3
  • Superoxide Dismutase
  • Nfe2l2 protein, rat
  • SIRT3 protein, rat
  • superoxide dismutase 2

Grants and funding

This work was supported by National Natural Science Foundation of China [Grant Number 81470019 to FSX].