Physical activity may drive healthy microvascular ageing via downregulation of p66 Shc

Narrower retinal arterioles and wider venules are linked to adverse cardiovascular outcomes. The mitochondrial adaptor p66; Shc; is a major source of ageing-induced generation of reactive oxygen species. Promoter DNA methylation inhibits p66; Shc; gene transcription. This cross-sectional study was designed to investigate the link between physical activity, retinal vessel diameters and p66; Shc; expression in active and sedentary ageing subjects.; Altogether 158 subjects were included in the study (mean age 59.4 ± 7.0 years). Thirty-eight subjects were healthy active, 36 were healthy sedentary and 84 were sedentary with ≥2 cardiovascular risk factors. Retinal arteriolar and venular diameters were measured by means of a retinal vessel analyser. As a marker of oxidative stress, plasma 3-nitrotyrosine was determined by enzyme-linked immunosorbent assay. Gene expression of p66; Shc; and DNA methylation were assessed in mononuclear cells by real-time quantitative polymerase chain reaction and methylated-DNA capture (MethylMiner Enrichment kit) coupled with quantitative polymerase chain reaction, respectively.; Wider retinal arterioles (179 ± 14 vs 172 ± 11 and 171 ± 14 µm;; p; < 0.05 and narrower venules (204 ± 17 vs 209 ± 11 and 218 ± 16 µm;; p; < 0.001) were observed in healthy active subjects compared with healthy sedentary subjects and sedentary subjects with ≥2 cardiovascular risk factors, respectively. Furthermore, healthy active subjects had blunted p66; Shc; expression and lower 3-nitrotyrosine plasma levels compared with healthy sedentary and sedentary subjects with ≥2 cardiovascular risk factors. Accordingly, hypomethylation of p66; Shc; promoter observed in healthy sedentary and sedentary subjects with ≥2 cardiovascular risk factors was not found in healthy active subjects.; Long-term physical activity-induced DNA methylation of p66; Shc; may represent a putative mechanistic link whereby active lifestyle promotes healthy microvascular ageing.