Key result
Single oral administration of 210 mg anthocyanin prevented smoking-induced decreases in flow-mediated dilation in young healthy smokers, but significantly elevated oxidative stress (d-ROMs) in non-smokers.
Why the study?
Does single oral administration of anthocyanin improve smoking-induced endothelial dysfunction and redox states in young healthy smokers?
Does single oral administration of anthocyanin improve smoking-induced endothelial dysfunction and redox states in young healthy smokers?
Absolute Event Rate: 9.5% vs 7.5%
A single dose of anthocyanin prevents smoking-induced endothelial dysfunction in young smokers but may paradoxically increase oxidative stress in healthy non-smokers.
May support acute endothelial protection in young smokers; leaves open paradoxical oxidative stress rise and needs larger trials before any use.
Objectives: Smoking causes endothelial dysfunction, but it still remains unclear whether oral administration of anthocyanin brings benefits to endothelial function and redox states in young healthy smokers. We tested the hypothesis that supplement anthocyanin may rescue endothelial dysfunction and redox states in young healthy smokers. Methods: Young healthy male non-smoker (n = 8) and smokers (n = 14) were enrolled to measure the derivatives of reactive oxygen metabolites (d-ROMs) and biological antioxidant potential (BAP) levels and brachial artery flow-mediated dilation (FMD) before and 2 hours after one cigarette smoking or resting under administration of blackcurrant supplements (anthocyanins 210 mg) or not. Results: FMD, d-ROMs, and BAP at baseline were similar between non-smokers and smokers. One cigarette smoking induced a decrease in FMD at 2 hours (9.0% ± 2.6% vs 7.5% ± 2.3%, p < 0.05) without affecting plasma levels of d-ROMs and BAP in young healthy smokers. Single oral administration of anthocyanin at 210 mg abolished smoking-induced decrease in FMD (8.3% ± 3.4% vs 9.5% ± 3.6%, p = ns) without changes in plasma levels of d-ROMs and BAP in young smokers. In non-smokers, however, administration of anthocyanin at 210 mg slightly but significantly elevated plasma level of d-ROMs at 2 hours (249.6 ± 30.3 vs 265.5 ± 36.3 U CARR, p < 0.05) without affecting plasma level of BAP and FMD. Conclusions: Single oral administration of anthocyanin rescued smoking-induced endothelial dysfunction in young healthy smokers, but facilitated oxidative stress in non-smokers. When anthocyanin is taken as supplements, it seems important to pay attention to the dose and timing of administration.
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Akane et al. (2018) studied Healthy young male smokers and non-smokers (n=22). Blackcurrant supplement (anthocyanin) vs. No supplement was evaluated on Brachial artery flow-mediated dilation (FMD) at 2 hours post-smoking. Single oral administration of 210 mg anthocyanin prevented smoking-induced decreases in flow-mediated dilation in young healthy smokers, but significantly elevated oxidative stress (d-ROMs) in non-smokers.
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