Literature DB >> 11181614

Cutaneous interstitial nitric oxide concentration does not increase during heat stress in humans.

C G Crandall1, D A MacLean.   

Abstract

Inhibition of cutaneous nitric oxide (NO) synthase reduces the magnitude of cutaneous vasodilation during whole body heating in humans. However, this observation is insufficient to conclude that NO concentration increases in the skin during a heat stress. This study was designed to test the hypothesis that whole body heating increases cutaneous interstitial NO concentration. This was accomplished by placing 2 microdialysis membranes in the forearm dermal space of 12 subjects. Both membranes were perfused with lactated Ringer solutions at a rate of 2 microl/min. In both normothermia and during whole body heating via a water perfused suit, dialysate from these membranes were obtained and analyzed for NO using the chemiluminescence technique. In six of these subjects, after the heat stress, the membranes were perfused with a 1 M solution of acetylcholine to stimulate NO release. Dialysate from these trials was also assayed to quantify cutaneous interstitial NO concentration. Whole body heating increased skin temperature from 34.6 +/- 0.2 to 38.8 +/- 0.2 degrees C (P < 0.05), which increased sublingual temperature (36.4 +/- 0.1 to 37.6 +/- 0.1 degrees C; P < 0.05), heart rate (63 +/- 5 to 93 +/- 5 beats/min; P < 0.05), and skin blood flow over the membranes (21 +/- 4 to 88 +/- 10 perfusion units; P < 0.05). NO concentration in the dialysate did not increase significantly during of the heat stress (7.6 +/- 0.7 to 8.6 +/- 0.8 microM; P > 0.05). After the heat stress, administration of acetylcholine in the perfusate significantly increased skin blood flow (128 +/- 6 perfusion units) relative to both normothermic and heat stress values and significantly increased NO concentration in the dialysate (15.8 +/- 2.4 microM). These data suggest that whole body heating does not increase cutaneous interstitial NO concentration in forearm skin. Rather, NO may serve in a permissive role in facilitating the effects of an unknown neurotransmitter, leading to cutaneous vasodilation during a heat stress.

Entities:  

Keywords:  NASA Discipline Cardiopulmonary; Non-NASA Center

Mesh:

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Year:  2001        PMID: 11181614     DOI: 10.1152/jappl.2001.90.3.1020

Source DB:  PubMed          Journal:  J Appl Physiol (1985)        ISSN: 0161-7567


  4 in total

1.  Venous but not skeletal muscle interstitial nitric oxide is increased during hypobaric hypoxia.

Authors:  Urs A Leuenberger; Douglas Johnson; Joseph Loomis; Kristen S Gray; David A MacLean
Journal:  Eur J Appl Physiol       Date:  2007-11-06       Impact factor: 3.078

2.  Nitric oxide is not permissive for cutaneous active vasodilatation in humans.

Authors:  Brad W Wilkins; Lacy A Holowatz; Brett J Wong; Christopher T Minson
Journal:  J Physiol       Date:  2003-03-21       Impact factor: 5.182

3.  Noninvasive assessment of vascular function in the posterior tibial artery of healthy humans.

Authors:  Christopher D Black; Bakari Vickerson; Kevin K McCully
Journal:  Dyn Med       Date:  2003-02-11

4.  The Effect of Being Aerobically Active vs. Inactive on Cutaneous Vascular Conductance during Local Heat Stress in an Older Population.

Authors:  Ulrike H Mitchell; Samantha Burton; Christopher Gordon; Gary W Mack
Journal:  Front Physiol       Date:  2017-10-31       Impact factor: 4.566

  4 in total

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