Enforced physical inactivity increases endothelial microparticle levels in healthy volunteers

Am J Physiol Heart Circ Physiol. 2010 Aug;299(2):H248-56. doi: 10.1152/ajpheart.00152.2010. Epub 2010 May 14.

Abstract

A sedentary lifestyle has adverse effects on the cardiovascular system, including impaired endothelial functions. Subjecting healthy men to 7 days of dry immersion (DI) presented a unique opportunity to analyze the specific effects of enhanced inactivity on the endothelium. We investigated endothelial properties before, during, and after 7 days of DI involving eight subjects. Microcirculatory functions were assessed with laser Doppler in the skin of the calf. We studied basal blood flow and endothelium-dependent and -independent vasodilation. We also measured plasma levels of microparticles, a sign of cellular dysfunction, and soluble endothelial factors, reflecting the endothelial state. Basal flow and endothelium-dependent vasodilation were reduced by DI (22 + or - 4 vs. 15 + or - 2 arbitrary units and 29 + or - 6% vs. 12 + or - 6%, respectively, P < 0.05), and this was accompanied by an increase in circulating endothelial microparticles (EMPs), which was significant on day 3 (42 + or - 8 vs. 65 + or - 10 EMPs/microl, P < 0.05), whereas microparticles from other cell origins remained unchanged. Plasma soluble VEGF decreased significantly during DI, whereas VEGF receptor 1 and soluble CD62E were unchanged, indicating that the increase in EMPs was associated with a change in antiapoptotic tone rather than endothelial activation. Our study showed that extreme physical inactivity in humans induced by 7 days of DI causes microvascular impairment with a disturbance of endothelial functions, associated with a selective increase in EMPs. Microcirculatory endothelial dysfunction might contribute to cardiovascular deconditioning as well as to hypodynamia-associated pathologies. In conclusion, the endothelium should be the focus of special care in situations of acute limitation of physical activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholine / administration & dosage
  • Administration, Cutaneous
  • Biomarkers / blood
  • Blood Glucose / metabolism
  • Cell-Derived Microparticles / pathology*
  • E-Selectin / blood
  • Endothelial Cells / drug effects
  • Endothelial Cells / metabolism
  • Endothelial Cells / pathology*
  • Endothelium, Vascular / drug effects
  • Endothelium, Vascular / metabolism
  • Endothelium, Vascular / pathology*
  • Endothelium, Vascular / physiopathology
  • Humans
  • Iontophoresis
  • Laser-Doppler Flowmetry
  • Leg
  • Lipids / blood
  • Male
  • Microcirculation
  • Nitroprusside / administration & dosage
  • Sedentary Behavior*
  • Skin / blood supply*
  • Time Factors
  • Vascular Endothelial Growth Factor A / blood
  • Vascular Endothelial Growth Factor Receptor-1 / blood
  • Vasodilation
  • Vasodilator Agents / administration & dosage
  • Weightlessness Simulation
  • Young Adult

Substances

  • Biomarkers
  • Blood Glucose
  • E-Selectin
  • Lipids
  • VEGFA protein, human
  • Vascular Endothelial Growth Factor A
  • Vasodilator Agents
  • Nitroprusside
  • FLT1 protein, human
  • Vascular Endothelial Growth Factor Receptor-1
  • Acetylcholine