Functional alterations in endothelial NO, PGI2 and EDHF pathways in aorta in ApoE/LDLR-/- mice

Gábor Csányi, Mariusz Gajda, Magdalena Franczyk-Zarow, Renata Kostogrys, Pawel Gwoźdź, Lukasz Mateuszuk, Magdalena Sternak, Luiza Wojcik, Teresa Zalewska, Michal Walski, Stefan Chlopicki

Research output: Contribution to journalArticle

34 Scopus citations

Abstract

Adequate endothelial production of nitric oxide (NO), endothelium-derived hyperpolarizing factor (EDHF), and prostacyclin (PGI2) is critical to the maintenance of vascular homeostasis. However, it is not clear whether alterations in each of these vasodilatory pathways contribute to the impaired endothelial function in murine atherosclerosis. In the present study, we analyze the alterations in NO-, EDHF- and PGI2-dependent endothelial function in the thoracic aorta in relation to the development of atherosclerotic plaques in apoE/LDLR-/- mice. We found that in the aorta of 2-month-old apoE/LDLR-/- mice there was no lipid deposition, subendothelial macrophage accumulation; and matrix metalloproteinase (MMP) activity was low, consistent with the absence of atherosclerotic plaques. Interestingly, at this stage the endothelium was already activated and hypertrophic as evidenced by electron microscopy, while acetylcholine-induced NO-dependent relaxation in the thoracic aorta was impaired, with concomitant upregulation of cyclooxygenase-2 (COX-2)/PGI2 and EDHF (epoxyeicosatrienoic acids, EETs) pathways. In the aorta of 3-6-month-old apoE/LDLR-/- mice, lipid deposition, macrophage accumulation and MMP activity in the intima were gradually increased, while impairment of NO-dependent function and compensatory upregulation of COX-2/PGI2 and EDHF pathways were more accentuated. These results suggest that impairment of NO-dependent relaxation precedes the development of atherosclerosis in the aorta and early upregulation of COX-2/PGI2 and EDHF pathways may compensate for the loss of the biological activity of NO.

Original languageEnglish (US)
Pages (from-to)107-115
Number of pages9
JournalProstaglandins and Other Lipid Mediators
Volume98
Issue number3-4
DOIs
StatePublished - Aug 1 2012
Externally publishedYes

Keywords

  • Atherosclerosis
  • EDHF
  • Endothelial dysfunction
  • Gene-targeted mice
  • Nitric oxide
  • Prostacyclin

ASJC Scopus subject areas

  • Biochemistry
  • Physiology
  • Pharmacology
  • Cell Biology

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  • Cite this

    Csányi, G., Gajda, M., Franczyk-Zarow, M., Kostogrys, R., Gwoźdź, P., Mateuszuk, L., Sternak, M., Wojcik, L., Zalewska, T., Walski, M., & Chlopicki, S. (2012). Functional alterations in endothelial NO, PGI2 and EDHF pathways in aorta in ApoE/LDLR-/- mice. Prostaglandins and Other Lipid Mediators, 98(3-4), 107-115. https://doi.org/10.1016/j.prostaglandins.2012.02.002