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Published on: May 14, 2013
Increased endogenous endothelin-1 in coronary circulation is associated with restenosis after coronary angioplasty
Hiroyuki Takase1, Masaya Sugiyama, Ai Nakazawa
1Enshu General Hospital, Hamamatsu, Japan. h_takase@ken.ja-shizouka.or.jp
Insights
Elevated endothelin-1 levels after percutaneous transluminal coronary angioplasty (PTCA) may signal an increased risk of coronary restenosis. This study investigated vasoactive substances as potential markers for restenosis post-PTCA.
Area of Science:
- Cardiology
- Vascular Biology
- Biomarker Discovery
Background:
- The role of vasoactive substances in coronary restenosis following percutaneous transluminal coronary angioplasty (PTCA) remains unclear.
- Investigating potential biomarkers is crucial for managing post-procedural complications.
Purpose of the Study:
- To ascertain if specific vasoactive substances can serve as indicators of coronary restenosis after PTCA.
- To analyze the association between endothelin-1, nitric oxide, serotonin, angiotensin II, and noradrenaline with restenosis.
Main Methods:
- Twenty-nine patients with angina pectoris underwent elective PTCA.
- Coronary angiography assessed lesion patency three months post-PTCA.
- Blood samples from the coronary sinus were collected before, immediately after, and three months after PTCA.
Main Results:
- Endothelin-1 levels were significantly higher immediately after and three months post-PTCA in the restenosis group compared to baseline.
- Nitrite/nitrate levels transiently decreased post-PTCA in both groups.
- Serotonin levels decreased in the patency group but not in the restenosis group; angiotensin II and noradrenaline showed no significant changes.
Conclusions:
- Endothelin-1 emerges as a potential marker associated with coronary restenosis after PTCA.
- Elevated endothelin-1 in coronary circulation post-PTCA may predict a higher risk of restenosis.
Background:
The relationship between vasoactive substances, including endothelin-1, nitric oxide, serotonin, angiotensin II and noradrenaline, and coronary restenosis after percutaneous transluminal coronary angioplasty (PTCA) is not clear.
Objective:
To determine whether any vasoactive substance may be a marker of coronary restenosis after PTCA.
Methods:
Twenty-nine patients with angina pectoris underwent elective PTCA. Three months after PTCA, coronary angiography was performed again to study the patency of the lesions. Seven patients had coronary restenosis (greater than 50% stenosis) (restenosis group) and the rest of the patients were without restenosis (patency group). Their blood samples were obtained from the coronary sinus before, immediately after and three months after PTCA.
Results:
Endothelin-1 levels obtained immediately after PTCA (3.44+/-0.26 pg/mL) and three months after PTCA (3.57+/-0.29 pg/mL) were significantly higher than those obtained before PTCA (3.00+/-0.26 pg/mL) in the restenosis group, but not in the patency group (3.34+/-0.15 pg/mL, 3.02+/-0.17 pg/mL and 3.14+/-0.18 pg/mL, respectively). A transient decrease in nitrite/nitrate levels was observed immediately after PTCA in both groups. The serotonin levels three months after PTCA were significantly decreased in the patency group, but not in the restenosis group, and the levels of angiotensin II and noradrenaline did not change in either group throughout the study.
Conclusions:
Among several vasoactive substances, endothelin-1 seems to be associated with the process of coronary restenosis after PTCA. Increased endothelin-1 levels in the coronary circulation after PTCA may indicate an increased risk of coronary restenosis.
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