Increased endothelial exocytosis and generation of endothelin-1 contributes to constriction of aged arteries

Aditya Goel, Baogen Su, Sheila Flavahan, Charles J. Lowenstein, Dan E. Berkowitz, Nicholas A. Flavahan

Research output: Contribution to journalArticlepeer-review

46 Scopus citations


Rationale: Circulating levels of endothelin (ET)-1 and endogenous ETA-mediated constriction are increased in human aging. The mechanisms responsible are not known. Objective: Investigate the storage, release, and activity of ET-1 system in arteries from young and aged Fischer-344 rats. Methods and results: After NO synthase inhibition (L-NAME), thrombin contracted aged arteries, which was inhibited by endothelial denudation, ETA receptor antagonism (BQ123), and ECE inhibition (phosphoramidon, SM19712) or by inhibiting exocytosis (TAT-NSF, N-ethylmaleimide-sensitive factor inhibitor). Thrombin did not cause endothelium-dependent contraction of young arteries. In aged but not young arteries, thrombin rapidly increased ET-1 release, which was abolished by endothelium denudation or TAT-NSF. L-NAME did not affect ET-1 release. ET-1 immunofluorescent staining was punctate and distinct from von Willebrand factor (VWF). VWF and ET-1 immunofluorescent intensity was similar in young and aged quiescent arteries. Thrombin rapidly increased ET-1 staining and decreased VWF staining in aged but had no effect in young aortas. After L-NAME, thrombin decreased VWF staining in young aortas. NO donor DEA-NONOate (1 to 100 nmol/L) reversed thrombin-induced exocytosis in young (VWF) but not aged L-NAME-treated aortas (VWF, ET-1). Expression of preproET-1 mRNA and ECE-1 mRNA were increased in aged compared to young endothelium. BigET-1 levels and contraction to exogenous BigET-1 (but not ET-1) were also increased in aged compared to young arteries. Conclusions: The stimulated exocytotic release of ET-1 is dramatically increased in aged endothelium. This reflects increased reactivity of exocytosis, increased expression and storage of ET-1 precursor peptides, and increased expression of ECE-1. Altered endothelial exocytosis of ET-1 and other mediators may contribute to cardiovascular pathology in aging.

Original languageEnglish (US)
Pages (from-to)242-251
Number of pages10
JournalCirculation research
Issue number2
StatePublished - Jul 23 2010


  • Weibel-Palade bodies
  • aorta
  • mesenteric arteries
  • thrombin
  • von Willebrand factor

ASJC Scopus subject areas

  • Physiology
  • Cardiology and Cardiovascular Medicine


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