Impaired effect of endothelin-1 on coronary artery stiffness in type 2 diabetes

Int J Cardiol. 2006 Sep 20;112(2):207-12. doi: 10.1016/j.ijcard.2005.09.018. Epub 2005 Dec 2.

Abstract

Aim: We examined whether there is a differential effect of endothelin-A antagonism on coronary artery compliance in type 2 diabetes mellitus compared to non-diabetic patients.

Patient and methods: We examined 32 patients, 11 type 2 diabetes mellitus and 21 non-diabetic patients, with atherosclerotic epicardial arteries free of significant luminal stenoses. Intracoronary BQ-123 (6 micromol), an endothelin-A receptor antagonist, was infused over 20 min. The artery lumen area in the proximal arterial segment was measured at end diastole and end systole before and after BQ-123 administration using an intravascular ultrasound catheter. Calculations were made of normalized arterial compliance index, in mm Hg(-1) x 10(3) and of arterial stiffness index beta.

Results: Pulse pressure and heart rate did not change after BQ-123. In type 2 diabetes mellitus, normalized compliance index decreased from 1.79+/-1.36 at baseline to 1.29+/-0.82 after BQ-123 administration, whereas in non-diabetic patients it increased from 2.10+/-1.36 to 3.00+/-2.07 (p<0.05 versus baseline) (F=6.39, p=0.02). In type 2 diabetes mellitus, beta index increased from 1.97+/-0.53 to 2.46+/-0.95, whereas in non-diabetic patients it decreased from 1.83+/-0.95 to 1.63+/-0.84 (F=7.80, p=0.009). Big endothelin-1 at baseline was correlated with the baseline beta index (p<0.0001, r=0.68).

Conclusions: Big endothelin-1 is correlated with the coronary artery stiffness. The effect of endogenous endothelin-1 on coronary artery stiffness is impaired in type 2 diabetes mellitus. This may have important therapeutic implications with respect to the introduction of endothelin receptor antagonists as cardiovascular therapeutic agents.

Publication types

  • Comparative Study

MeSH terms

  • Aged
  • Aldosterone / blood
  • Compliance
  • Coronary Vessels / diagnostic imaging
  • Coronary Vessels / physiopathology*
  • Diabetes Mellitus, Type 2 / blood*
  • Diabetes Mellitus, Type 2 / physiopathology*
  • Endothelin Receptor Antagonists
  • Endothelin-1 / blood*
  • Female
  • Humans
  • Male
  • Middle Aged
  • Peptides, Cyclic / pharmacology
  • Pericardium
  • Prospective Studies
  • Pulsatile Flow
  • Renin / blood
  • Ultrasonography, Interventional

Substances

  • Endothelin Receptor Antagonists
  • Endothelin-1
  • Peptides, Cyclic
  • Aldosterone
  • Renin
  • cyclo(Trp-Asp-Pro-Val-Leu)