Protective Role of Short-term Aerobic Exercise Against Zinc Oxide Nanoparticles-Induced Cardiac Oxidative Stress Via Possible Changes of Apelin, Angiotensin II/Angiotensin II Type I Signalling Pathway

Cardiovasc Toxicol. 2023 Jun;23(5-6):177-184. doi: 10.1007/s12012-023-09792-8. Epub 2023 May 15.

Abstract

This study examined the protective role of short-term aerobic exercise on ZnO NPs-induced cardiac oxidative stress and possible changes of apelin, angiotensin II (AngII) and angiotensin II type I receptor (AT1R) signalling pathway. Thirty-five male Wistar rats were randomized into five groups of seven rats, including control, saline, ZnO NPs, exercise and exercise + ZnO NPs groups. The animal in ZnO NPs and exercise + ZnO NPs groups received 1 mg/kg of ZnO NPs. Rats underwent the treadmill exercise program. Treatments lasted four weeks, 5 days/week. After 4 weeks of treatment, superoxide dismutase (SOD) activity, malondialdehyde (MDA), apelin, Ang II and AT1R concentration were measured in heart tissue.Cardiac MDA, Ang II and AT1R levels significantly increased while SOD activity and apelin levels significantly decreased following ZnO NPs administration. The aerobic exercise induced a significant increase in the SOD activity and apelin levels and a significant decrease in the enhanced MDA, Ang II and AT1R levels in the heart of ZnO NPs-exposed rats. These results suggest that the exercise-induced attenuation of the Ang II-AT1R signalling pathway is mediated by reduced lipid peroxidation, augmented antioxidant defence and enhanced apelin synthesis that may be a protective mechanism to prevent and/or treatment ZnO NPs-induced cardiac oxidative stress.

Keywords: Angiotensin II; Apelin; Heart; Oxidative stress; Zinc oxide (ZnO) nanoparticles.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angiotensin II / analysis
  • Animals
  • Apelin / analysis
  • Exercise Therapy*
  • Heart / physiology
  • Lipid Peroxidation
  • Models, Animal
  • Myocardium* / chemistry
  • Nanoparticles* / toxicity
  • Oxidative Stress / drug effects
  • Random Allocation
  • Rats
  • Rats, Wistar
  • Receptor, Angiotensin, Type 1 / analysis
  • Signal Transduction
  • Superoxide Dismutase / analysis
  • Thiobarbituric Acid Reactive Substances / analysis
  • Zinc Oxide* / toxicity

Substances

  • Zinc Oxide
  • Superoxide Dismutase
  • Apelin
  • Angiotensin II
  • Agtr1a protein, rat
  • Thiobarbituric Acid Reactive Substances
  • Receptor, Angiotensin, Type 1