4.5 Article

Optical coherence tomography in the assessment of acute changes in cutaneous vascular diameter induced by heat stress

Journal

JOURNAL OF APPLIED PHYSIOLOGY
Volume 121, Issue 4, Pages 965-972

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/japplphysiol.00918.2015

Keywords

skin microvessels; optical coherence tomography; laser Doppler

Funding

  1. National Health and Medical Research Council, Australia
  2. Chevron Australia
  3. Fiona Wood Foundation
  4. National Heart Foundation
  5. Australian Research Council [DP 130103793, DP 160104175]

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There are limited imaging technologies available that can accurately assess or provide surrogate markers of the in vivo cutaneous microvessel network in humans. In this study, we establish the use of optical coherence tomography (OCT) as a novel imaging technique to assess acute changes in cutaneous microvessel area density and diameter in humans. OCT speckle decorrelation images of the skin on the ventral side of the forearm up to a depth of 500 mu m were obtained prior to and following 20-25 min of lower limb heating in eight healthy men [30.3 +/- 7.6 (SD) yr]. Skin red blood cell flux was also collected using laser Doppler flowmetry probes immediately adjacent to the OCT skin sites, along with skin temperature. OCT speckle decorrelation images were obtained at both baseline and heating time points. Forearm skin flux increased significantly (0.20 +/- 0.15 to 1.75 +/- 0.38 cutaneous vascular conductance, P < 0.01), along with forearm skin temperature (32.0 +/- 1.2 to 34.3 +/- 1.0 degrees C, P < 0.01). Quantitative differences in the automated calculation of vascular area densities (26 +/- 9 to 49 +/- 19%, P < 0.01) and individual microvessel diameters (68 +/- 17 to 105 +/- 25 mu m, P < 0.01) were evident following the heating session. This is the first in vivo within- subject assessment of acute changes in the cutaneous microvasculature in response to heating in humans and highlights the use of OCT as an exciting new imaging approach for skin physiology and clinical research.

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