Renal denervation ameliorates post-infarction cardiac remodeling in rats through dual regulation of oxidative stress in the heart and brain

Biomed Pharmacother. 2019 Oct:118:109243. doi: 10.1016/j.biopha.2019.109243. Epub 2019 Jul 23.

Abstract

Background: Myocardial remodeling is the key step in the development of ischemic cardiomyopathy. We aimed to compare effects of renal denervation (RDN) with those of angiotensin receptor neprilysin inhibitors (ARNi) on cardiac remodeling after myocardial infarction (MI), and explore underlying mechanism.

Methods: Sprague-Dawley rats (n = 40; male) were subjected to ligation of left anterior descending coronary artery to induce MI; six rats served as controls. ARNi was administered at a dose of 60 mg/kg/day for 4 weeks starting 1 week after MI. An RDN/Sham-RDN procedure was performed 1 week after MI. Rats in all groups were studied 5 weeks after MI. Echocardiography was used to evaluate cardiac function. Masson staining and TUNEL staining were used to determine the extent of cardiac remodeling. Indicators of oxidative stress in heart and brain were used to analyze the potential mechanisms involved.

Results: Five weeks after MI, both RDN and ARNi significantly improved cardiac function and cardiac remodeling; however, RDN was superior to ARNi at attenuating myocardial apoptosis. Compared to ARNi, RDN was also more effective at decreasing the abnormal oxidative stress caused by MI; this was especially true in case of the brain and was confirmed by evaluating the changes in reactive oxygen species (ROS) levels and other oxidative stress parameters following MI.

Conclusions: RDN is not inferior to ARNi with respect to the improvement of cardiac remodeling in rats with ischemic cardiomyopathy. The effect of RDN might be associated with effective inhibition of oxidative stress in both the heart and brain.

Keywords: Angiotensin receptor neprilysin inhibitors; Cardiac remodeling; Hypothalamus; Oxidative stress; Renal denervation.

MeSH terms

  • Animals
  • Brain / pathology*
  • Enzyme Inhibitors / pharmacology
  • Hypothalamus / pathology
  • Kidney / drug effects
  • Kidney / innervation*
  • Male
  • Myocardial Infarction / pathology
  • Myocardial Infarction / physiopathology*
  • Myocardium / pathology*
  • Neprilysin / antagonists & inhibitors
  • Oxidative Stress* / drug effects
  • Rats, Sprague-Dawley
  • Sympathetic Nervous System / drug effects
  • Sympathetic Nervous System / pathology
  • Tyrosine 3-Monooxygenase / metabolism
  • Ventricular Remodeling* / drug effects

Substances

  • Enzyme Inhibitors
  • Tyrosine 3-Monooxygenase
  • Neprilysin