4.6 Article

Vascular response to 1 week of sleep restriction in healthy subjects. A metabolic response?

Journal

INTERNATIONAL JOURNAL OF CARDIOLOGY
Volume 190, Issue -, Pages 246-255

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.ijcard.2015.04.119

Keywords

Sleep; Inflammation; Endothelial function; Iontophoresis; Laser doppler; Sleep restriction

Funding

  1. French General Directorate for Armament (DGA, Ministry of Defence) [PDH-1-SMO-2-505/12co706]

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Background: Sleep loss may induce endothelial dysfunction, a key factor in cardiovascular risk. We examined the endothelial function during one week of sleep restriction and a recovery period (from 3-to-13 days) in healthy subjects, and its link to autonomic, inflammatory and/or endocrine responses. Methods: 12 men were followed at baseline (B1, 8-h sleep), after 2 (SR2) and 6 (SR6) days of SR (4-h sleep: 02:00-06:00) and after 1 (R1) and 12 (R12) recovery nights (8 h sleep). At 10: 00, we assessed changes in: arm cutaneous vascular conductance (CVC) induced by local application of methacholine (MCh), cathodal current (CIV) and heat (44 degrees C), finger CVC and skin temperature (Tfi) during local cold exposure (5 degrees C, 20-min) and passive recovery (22 degrees C, 20-min). Blood samples were collected at 08:00. Results: Compared with baseline (B1), MCh and heat-induced maximal CVC values (CVCpeak) were decreased at SR6 and R1. No effect of SRwas observed for Tfi and CVC during immersion whereas these values were lower during passive recovery on SR6 and R1. From SR2 to R12, plasma concentrations of insulin, IGF-1 (total and free) and MCP-1 were significantly increased while those of testosterone and prolactin were decreased. Whole-blood blood mRNA concentrations of TNF-alpha and IL-1 beta were higher than B1. No changes in noradrenaline concentrations, heart rate and blood pressure were observed. Conclusions: These results demonstrate that SR reduces endothelial-dependent vasodilatation and local tolerance to cold. This endothelial dysfunction is independent of blood pressure and sympathetic activity but associated with inflammatory and metabolic pathway responses. (C) 2015 Elsevier Ireland Ltd. All rights reserved.

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