Maternal NO2 exposure induces cardiac hypertrophy in male offspring via ROS-HIF-1α transcriptional regulation and aberrant DNA methylation modification of Csx/Nkx2.5

Arch Toxicol. 2018 Apr;92(4):1563-1579. doi: 10.1007/s00204-018-2166-3. Epub 2018 Feb 7.

Abstract

Maternal exposure to nitrogen dioxide (NO2) poses a risk for morbidity and mortality in infantile congenital heart diseases and even adult cardiovascular diseases. However, the experimental evidence supporting these effects is insufficient, and the related regulatory mechanisms are unknown. In the present study, we aimed to determine whether maternal NO2 exposure causes cardiac hypertrophy-related consequences in offspring, and if so, how these adverse effects occur in the postnatal heart. The results indicate that in mice, maternal NO2 exposure causes cardiac hypertrophy in male offspring. This altered phenotype was accompanied by increased expression of atrial natriuretic peptide, B-type natriuretic peptide, bone morphogenetic protein 10 and β-myosin heavy chain and elevated activities of cardiomyocyte injury markers, including serum glutamate-oxaloacetate transaminase, lactate dehydrogenase and kinases creatine phosphokinase (CK-MB) in serum. The cardiac-specific transcription factor Csx/Nkx2.5 played an important role in the induction of cardiac hypertrophy and cardiomyocyte injury, and the action was associated with ROS-HIF-1α transcriptional regulation and DNA hypomethylation modification.

Keywords: Cardiac hypertrophy; Csx/Nkx2.5; DNA hypomethylation modification; Maternal NO2 exposure; ROS-HIF-1α transcriptional regulation.

MeSH terms

  • Animals
  • Aspartate Aminotransferases / blood
  • Atrial Natriuretic Factor / blood
  • Biomarkers / blood
  • Bone Morphogenetic Proteins / blood
  • Cardiomegaly / chemically induced*
  • Cardiomegaly / genetics
  • Creatine Kinase / blood
  • DNA Methylation
  • Female
  • Gene Expression Regulation
  • Homeobox Protein Nkx-2.5 / genetics*
  • Humans
  • Hypoxia-Inducible Factor 1, alpha Subunit / genetics*
  • L-Lactate Dehydrogenase / blood
  • Male
  • Maternal Exposure*
  • Mice
  • Natriuretic Peptide, Brain / blood
  • Nitrogen Dioxide / toxicity*
  • Pregnancy
  • Reactive Oxygen Species / metabolism*
  • Ventricular Myosins / blood

Substances

  • Biomarkers
  • Bmp10 protein, mouse
  • Bone Morphogenetic Proteins
  • Hif1a protein, mouse
  • Homeobox Protein Nkx-2.5
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Reactive Oxygen Species
  • Natriuretic Peptide, Brain
  • Atrial Natriuretic Factor
  • L-Lactate Dehydrogenase
  • Aspartate Aminotransferases
  • Creatine Kinase
  • Ventricular Myosins
  • Nitrogen Dioxide