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Published on: May 26, 2022
Candesartan improves impaired endothelial function in the human coronary artery
Kenji Iino1, Hiroyuki Watanabe, Takako Iino
1Department of Cardiovascular and Respiratory Medicine, Akita University Graduate School of Medicine, Hondoh, Japan.
Insights
Candesartan treatment significantly improved coronary endothelial function in patients with endothelial dysfunction, as measured by coronary blood flow velocity reserve. This improvement was associated with a reduced risk of cardiovascular events.
Area of Science:
- Cardiology
- Vascular Biology
- Pharmacology
Background:
- Endothelial dysfunction is a key factor in cardiovascular events.
- Angiotensin II type 1 receptor blockers (ARB) are known to improve peripheral endothelial function.
- The impact of ARBs on coronary endothelial function remains largely uninvestigated.
Purpose of the Study:
- To evaluate the efficacy of ARB therapy in improving human coronary artery endothelial function.
- To determine if candesartan can reverse coronary endothelial dysfunction.
Main Methods:
- A randomized controlled trial involving 27 patients with coronary endothelial dysfunction.
- Treatment with candesartan (n=14) or placebo (n=13) for 12 months.
- Coronary endothelial function assessed by coronary blood flow velocity reserve (CFR) using Doppler-tipped guide-wire and acetylcholine infusion.
Main Results:
- Baseline CFR was below 300% in both groups, indicating endothelial dysfunction.
- Candesartan significantly increased CFR after 6 months (199% to 337%, P<0.001), while the control group showed no change (194% to 185%, P=0.52).
- Increased CFR correlated with a higher cardiovascular event-free survival rate (P=0.02), and the candesartan group had better event-free survival than the control group (P=0.04).
Conclusions:
- Candesartan effectively improves coronary endothelial dysfunction in human coronary arteries.
- The use of candesartan may serve as a strategy to prevent cardiac events in patients with endothelial dysfunction.
Background:
Endothelial dysfunction is closely related to cardiovascular events. Several studies have documented that angiotensin II type 1 receptor blockers (ARB) improve peripheral endothelial dysfunction. However, the effect of ARB on coronary endothelial function remains elusive. The purpose of this study was to ascertain the beneficial effects of ARB on human coronary artery endothelial function.
Methods And Results:
Twenty-seven patients were randomly assigned to either the candesartan group (n=14) or the control group (n=13) and followed for 12 months. Coronary blood flow velocity was measured in the left anterior descending artery without stenosis using an intracoronary Doppler-tipped guide-wire. We evaluated coronary endothelial function as the coronary blood flow velocity reserve (CFR), which was defined as the percent change in the coronary blood flow velocity after an intracoronary acetylcholine infusion. At baseline, the CFR in both groups was below 300%, implying that these patients had endothelial dysfunction. After treatment with candesartan for 6 months, the CFR increased significantly from 199 ± 20 to 337 ± 27% (P<0.001), whereas the CFR did not change in the control group (194 ± 32 vs. 185 ± 41%, P=0.52). During 12 months of observation, the cardiovascular event-free survival rate of the patients with an increased CFR was significantly greater than the rate in patients with a decreased CFR (P=0.02). Moreover, the cardiovascular event-free survival rate was greater in the candesartan group than in the control group (P=0.04).
Conclusion:
Our results suggest that candesartan improves coronary endothelial dysfunction of human coronary arteries and may prevent cardiac events.
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