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Updated: Jul 6, 2026

Assessing Endothelial Vasodilator Function with the Endo-PAT 2000
Published on: October 15, 2010
Effects of long-term nicorandil administration on endothelial function, inflammation, and oxidative stress in
Yutaka Ishibashi1, Nobuyuki Takahashi, Atsushi Tokumaru
1Division of Cardiovascular Medicine, Department of Internal Medicine, Shimane University Faculty of Medicine, Shimane, Japan. yuyu@med.shimane-u.ac.jp
Insights
Long-term nicorandil therapy improves endothelial function and cardiovascular health. This cardioprotective effect is linked to reduced oxidative stress and systemic inflammation in patients with cardiovascular risk factors.
Area of Science:
- Cardiovascular Medicine
- Pharmacology
Background:
- Long-term nicorandil administration shows cardioprotective effects in coronary artery disease.
- Understanding the mechanisms behind nicorandil's benefits is crucial for cardiovascular risk management.
Purpose of the Study:
- To investigate the impact of long-term nicorandil on endothelial function, systemic inflammation, and oxidative stress.
- To elucidate the pleiotropic mechanisms of nicorandil in patients with cardiovascular risk factors.
Main Methods:
- A randomized controlled trial involving 53 patients with cardiovascular risk factors.
- Assessed flow-mediated vasodilatation (FMD), malondialdehyde-modified low-density lipoprotein (MDA-LDL), and high-sensitivity C-reactive protein (hs-CRP) over 12 months.
- Compared nicorandil therapy (15 mg/day) with usual care.
Main Results:
- Nicorandil group showed significant improvement in FMD at 12 months compared to the control group.
- MDA-LDL levels were significantly reduced in the nicorandil group, while hs-CRP levels decreased at 6 and 12 months.
- No significant changes in FMD, MDA-LDL, or hs-CRP were observed in the non-nicorandil group.
Conclusions:
- Long-term nicorandil therapy gradually improves endothelial function.
- Nicorandil may offer cardiovascular protection via pleiotropic effects, including reduced oxidative stress and inflammation.
Abstract:
Long-term administration of nicorandil has been shown to improve outcomes through cardioprotective effects in patients with coronary artery disease. To identify the mechanisms responsible for these effects, this study examined the impact of long-term nicorandil administration on endothelial function, systemic inflammatory markers, and oxidative stress in patients with cardiovascular risk factors. Fifty-three patients were assigned to receive either nicorandil therapy (15 mg/day; n = 26) (nicorandil group) or usual care (n = 27) (nonnicorandil group). All study participants underwent flow-mediated vasodilatation (FMD) of the brachial artery 1 month before treatment, just before treatment, and at 3, 6, and 12 months following treatment. At identical time points, serum levels of malondialdehyde-modified low-density lipoprotein (MDA-LDL) and high-sensitivity C-reactive protein (hs-CRP) were collected. Compared with the nonnicorandil group, the nicorandil group demonstrated significantly increased FMD at 12 months, a finding not replicated for endothelium-independent vasodilatation with nitroglycerine. Analysis of biochemical markers revealed significantly reduced MAD-LDL levels in the nicorandil group at 12 months, as compared to slightly increased MAD-LDL levels in the nonnicorandil group. Significant reductions in hs-CRP levels were also noted at 6 and 12 months in the nicorandil group, while no change was found in the nonnicorandil group. Results demonstrated that long-term nicorandil therapy is associated with gradual improvements in endothelial function. Our findings also suggest that nicorandil treatment may result in cardiovascular protection through pleiotropic effects including reductions in oxidative injury and systemic inflammation.
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