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Antioxidant vitamin C prevents decline in endothelial function during sitting
Saurabh S Thosar1, Sylvanna L Bielko1, Chad C Wiggins1
1Department of Kinesiology, Indiana University School of Public Health, Indiana University, Bloomington, IN, USA.
Insights
Antioxidant Vitamin C supplementation prevented endothelial dysfunction caused by prolonged sitting. This suggests that oxidative stress contributes to impaired blood vessel function during extended sedentary periods.
Area of Science:
- Cardiovascular Physiology
- Nutritional Science
- Oxidative Stress Research
Background:
- Prolonged sitting impairs endothelial function, a critical aspect of cardiovascular health.
- The role of oxidative stress in this impairment is not fully understood.
Purpose of the Study:
- To investigate whether antioxidant Vitamin C can prevent endothelial dysfunction induced by 3 hours of sitting.
- To explore the potential contribution of oxidative stress to sedentary behavior-induced vascular changes.
Main Methods:
- A randomized controlled trial involving 11 healthy men.
- Participants underwent two 3-hour sitting trials: one without Vitamin C (SIT) and one with Vitamin C supplementation (VIT).
- Superficial femoral artery (SFA) flow-mediated dilation (FMD) was measured hourly to assess endothelial function.
Main Results:
- Three hours of sitting significantly reduced SFA FMD and shear rates.
- Vitamin C supplementation (VIT) significantly prevented the decline in SFA FMD at 1, 2, and 3 hours compared to the SIT trial.
- No significant differences in shear rates were observed between the SIT and VIT trials.
Conclusions:
- Three hours of sitting leads to impaired endothelial function in the superficial femoral artery.
- Antioxidant Vitamin C effectively prevented this impairment, indicating a role for oxidative stress.
- Vitamin C supplementation may be a viable strategy to mitigate the vascular effects of prolonged sitting.
Background:
This study was designed to test the hypothesis that antioxidant Vitamin C prevents the impairment of endothelial function during prolonged sitting.
Material And Methods:
Eleven men (24.2 ± 4.4 yrs) participated in 2 randomized 3-h sitting trials. In the sitting without vitamin C (SIT) and the sitting with vitamin C (VIT) trial, participants were seated for 3 h without moving their legs. Additionally, in the VIT trial, participants ingested 2 vitamin C tablets (1 g and 500 mg) at 30 min and 1 h 30 min, respectively. Superficial femoral artery (SFA) flow-mediated dilation (FMD) was measured hourly for 3 h.
Results:
By a 1-way ANOVA, there was a significant decline in FMD during 3 h of SIT (p<0.001). Simultaneously, there was a significant decline in antegrade (p=0.04) and mean (0.037) shear rates. For the SIT and VIT trials by a 2-way (trial x time) repeated measures ANOVA, there was a significant interaction (p=0.001). Pairwise testing revealed significant between-SFA FMD in the SIT and VIT trial at each hour after baseline, showing that VIT prevented the decline in FMD 1 h (p=0.009), 2 h (p=0.016), and 3 h (p=0.004). There was no difference in the shear rates between SIT and VIT trials (p>0.05).
Conclusions:
Three hours of sitting resulted in impaired SFA FMD. Antioxidant Vitamin C prevented the decline in SFA FMD, suggesting that oxidative stress may contribute to the impairment in endothelial function during sitting.
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