Preliminary analysis of the association of TRPV1 to the formation of Marfan syndrome aneurysms

Histol Histopathol. 2019 Dec;34(12):1329-1343. doi: 10.14670/HH-18-127. Epub 2019 May 10.

Abstract

Marfan syndrome (MS) is an autosomal dominant disorder of connective tissue that is caused by mutations in the fibrillin-1 (FBN-1) gene that cause degeneration of the artery. It is accompanied by endothelial dysfunction. The potential transient receptor of the vanilloid subfamily 1 (TRPV1) ion channel plays an important role in endothelial vascular functioning. Here we determine the association of the presence TRPV1 in aortic aneurysm with dilation and dissection of the artery in MS patients. Histological sections of aortic aneurysm tissue obtained by the surgical procedure of Bentall and De Bono or David, were processed by immunohistochemistry with antibodies against ICAM, VCAM, iNOS, eNOS, TRPV1 and TNF-α and the immunolabelling area was determined. We also measured the NO₃⁻/NO₂⁻ ratio in the aortic tissue. C-reactive protein and HDL in plasma were quantified. A significant increase in iNOS, TRPV1, VCAM (p≤0.05), NO₃⁻/NO₂⁻ ratio (p=0.002) and a significant decrease in eNOS (p=0.04) and HDL in plasma (p=0.02) in the MS vs. the C group were found. Conclusion: TRPV1 is over-expressed in aortic tissue from MS patients and can be associated with increases in iNOS, VCAM and a decrease in eNOS. These changes might contribute to the progression and rupture of the thoracic aneurysm.

Publication types

  • Comparative Study
  • Observational Study

MeSH terms

  • Adult
  • Aneurysm / genetics*
  • Aortic Aneurysm, Thoracic / metabolism
  • C-Reactive Protein / metabolism
  • Disease Progression
  • Female
  • Fibrillin-1 / genetics
  • Gene Expression Regulation
  • Humans
  • Immunohistochemistry
  • Inflammation
  • Intercellular Adhesion Molecule-1 / metabolism
  • Lipoproteins, HDL / metabolism
  • Male
  • Marfan Syndrome / genetics*
  • Marfan Syndrome / pathology
  • Middle Aged
  • Nitric Oxide Synthase Type III / metabolism
  • Nitrogen Dioxide / chemistry
  • Nitrogen Oxides / chemistry
  • Phenotype
  • TRPV Cation Channels / genetics*
  • Vascular Cell Adhesion Molecule-1 / metabolism

Substances

  • FBN1 protein, human
  • Fibrillin-1
  • ICAM1 protein, human
  • Lipoproteins, HDL
  • Nitrogen Oxides
  • TRPV Cation Channels
  • TRPV1 protein, human
  • Vascular Cell Adhesion Molecule-1
  • Intercellular Adhesion Molecule-1
  • nitrogen trioxide
  • C-Reactive Protein
  • NOS3 protein, human
  • Nitric Oxide Synthase Type III
  • Nitrogen Dioxide

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