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. 2017 Aug 6;3(1):e000248.
doi: 10.1136/bmjsem-2017-000248. eCollection 2017.

Interval exercise increases angiogenic cell function in postmenopausal women

Affiliations

Interval exercise increases angiogenic cell function in postmenopausal women

Emma Harris et al. BMJ Open Sport Exerc Med. .

Abstract

Introduction: Exercise can help to negate the increased cardiovascular disease risk observed in women after the menopausal transition. This study sought to determine whether interval or continuous exercise has differential effects on endothelial function and circulating angiogenic cell (CAC) number and function in postmenopausal women.

Methods: Fifteen healthy postmenopausal women completed a 30 min acute moderate-intensity continuous (CON) and interval exercise (MOD-INT) session on a cycle ergometer on separate days. Nine participants completed a further single 30 min acute heavy-intensity interval (HEAVY-INT) exercise session. Brachial artery flow-mediated dilation (FMD) was assessed pre-exercise and 15 min post-exercise session. CAC number and colony-forming capacity in vitro were assessed post exercise and compared with resting levels.

Results: FMD and CAC number did not change post exercise regardless of exercise type (p>0.05). However, the number (mean±SD) of colony-forming units (CFUs) increased from visit 1 (12±10 CFUs/well) to post MOD-INT (32±30 CFUs/well) and post HEAVY-INT (38±23 CFUs/well) but not post CON (13±14 CFUs/well).

Conclusion: A single session of interval exercise is more effective than a continuous exercise session for increasing the intercellular communication of CACs, regardless of exercise intensity. The enhanced ability of CACs to form colonies may reflect an increased number and/or function of angiogenic T-cells. The repeated exertions to higher work rates during interval exercise may explain this response. Repeated exercise sessions might be required to improve FMD in postmenopausal women.

Keywords: circulating angiogenic cells; endothelial function; interval and continuous exercise; menopause.

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Conflict of interest statement

Competing interests: None declared.

Figures

Figure 1
Figure 1
The number (mean with 95% CI) of colony-forming units (CFUs) at visit 1 and following a 30 min moderate-intensity continuous (CON), moderate-intensity interval (MOD-INT) and heavy-intensity interval (HEAVY-INT) exercise bout. CFUs increased following the MOD-INT (n=14) and the HEAVY-INT (n=9) exercise bouts, but not following CON (n=14).

References

    1. Taddei S, Virdis A, Ghiadoni L, et al. . Menopause is associated with endothelial dysfunction in women. Hypertension 1996;28:576–82. 10.1161/01.HYP.28.4.576 - DOI - PubMed
    1. Rakobowchuk M, Harris E, Taylor A, et al. . Heavy and moderate interval exercise training alters low-flow-mediated constriction but does not increase circulating progenitor cells in healthy humans. Exp Physiol 2012;97:375–85. 10.1113/expphysiol.2011.062836 - DOI - PMC - PubMed
    1. Aragona CO, Imbalzano E, Mamone F, et al. . Endothelial Progenitor Cells for Diagnosis and Prognosis in Cardiovascular Disease. Stem Cells Int 2016;2016:1–12. 10.1155/2016/8043792 - DOI - PMC - PubMed
    1. Hill JM, Zalos G, Halcox JP, et al. . Circulating endothelial progenitor cells, vascular function, and cardiovascular risk. N Engl J Med 2003;348:593–600. 10.1056/NEJMoa022287 - DOI - PubMed
    1. Kunz GA, Liang G, Cuculi F, et al. . Circulating endothelial progenitor cells predict coronary artery disease severity. Am Heart J 2006;152:190–5. 10.1016/j.ahj.2006.02.001 - DOI - PubMed