Regular exercise delays microvascular endothelial dysfunction by regulating antioxidant capacity and cellular metabolism

Abstract

Aging is the basis for several unfavorable conditions, including cardiovascular diseases (CVDs). In this sense, regular physical activity (regular PA) has been proven to delay cellular aging and prevent endothelial dysfunction related to CVDs. Despite numerous studies involving athletes, little is known about cellular and molecular mechanisms of regular PA among master athletes. The present study aimed at evaluating the effects of regular PA on local microcirculatory functions in elderly athletes as compared to age-matched sedentary controls. Moreover, molecular/epigenetic mechanisms (nitric oxide, oxidative stress, PGC-1α, SIRT1 and miR29) were also assessed. The results of the present study showed that regular PA significantly increased local blood flow in post-ischemia and post-heating conditions, as well as NO plasma concentrations, denoting a better endothelial function/microcirculatory efficiency. Moreover, athletes presented a greater plasma antioxidant and increased transcriptional levels of the metabolism regulator PGC-1α. Finally, regular PA enhanced plasma level of SIRT1 and miR29, suggested as epigenetic regulators of redox balance and cellular metabolism. In addition, stimulated local blood flow was directly related to plasma antioxidant capacity, and SIRT1 and miR29 levels. Overall, our data confirm the beneficial effects of regular PA on the cardiovascular profile in elderly athletes and shed light on molecular signals involved in the positive adaptations to exercise.

Figure 1

Descriptive statistics of selected parameters for ATL and SED. The data are reported as mean ± SD. Statistical analysis was performed by unpaired t-tests: **p < 0.01, ***p < 0.001 (ATL vs. SED). HBF (Hand Blood Flow); FBF (Foot Blood Flow); NOx (Nitric Oxide); TOSC (Total Oxyradical Scavenging Capacity); PGC-1α (PPAR-γ co-activator-1 α); SIRT1 (Sirtuin 1).