Effect of Intake Duration of Anthocyanin-Rich New Zealand Blackcurrant Extract on Cardiovascular Responses and Femoral Artery Diameter during Sustained Submaximal Isometric Contraction
Matthew D. Cook, Aaron Dunne, Michael Bosworth, Mark E. T. Willems
Abstract
Seven-day intake of anthocyanins from New Zealand blackcurrant (NZBC) extract increased cardiac output and femoral artery diameter during a sustained submaximal isometric contraction. It is not known if there are intake duration effects by NZBC extract on the isometric contraction-induced cardiovascular responses. In a repeated measures design, male participants (n = 19, age: 26 ± 4 years) performed a 120-second submaximal (30%) isometric contraction of the knee extensors at baseline and following 1, 4 and 7-days intake of 600 mg·day−1 NZBC extract. During the 120-second submaximal isometric contraction, femoral artery diameter and cardiovascular responses were measured with ultrasound and beat-to-beat hemodynamic monitoring. Femoral artery was larger following 4-days (mean difference = 0.046 cm, 95% CI [0.012, 0.080], p = 0.005) and 7-days (mean difference = 0.078 cm, 95% CI [0.034, 0.123], p < 0.001) in comparison to baseline with no increase with 1-day intake. Systolic and diastolic blood pressure, heart rate and total peripheral resistance were not changed by NZBC extract at 1, 4 and 7-days intake. However, mean arterial pressure, stroke volume, cardiac output and total peripheral resistance were changed at time points during the isometric contraction following 7-days intake in comparison to 1-day intake of NZBC extract (p < 0.05). Alterations in femoral artery diameter and some cardiovascular responses during a submaximal sustained isometric contraction of the knee extensors are affected by the intake duration of New Zealand blackcurrant extract, with no effects by 1-day intake. Our observations suggest that the bioavailability of blackcurrant anthocyanins and anthocyanin-derived metabolites is required for days to alter the mechanisms for isometric-contraction induced cardiovascular responses.