Venous but not skeletal muscle interstitial nitric oxide is increased during hypobaric hypoxia
Autor: | Urs A. Leuenberger, Joseph L. Loomis, Kristen S. Gray, David A. MacLean, Douglas Johnson |
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Rok vydání: | 2007 |
Předmět: |
Adult
Male Atmosphere Exposure Chambers medicine.medical_specialty Physiology Microdialysis Vasodilation Nitric Oxide Veins Nitric oxide chemistry.chemical_compound Physiology (medical) Internal medicine Extracellular fluid medicine Humans Orthopedics and Sports Medicine Hypoxia Muscle Skeletal Altitude Public Health Environmental and Occupational Health Skeletal muscle Extracellular Fluid Venous Plasma General Medicine Anatomy Hypoxia (medical) Adenosine Oxygen Forearm medicine.anatomical_structure Endocrinology chemistry Hypobaric chamber medicine.symptom medicine.drug |
Zdroj: | European Journal of Applied Physiology. 102:457-461 |
ISSN: | 1439-6327 1439-6319 |
DOI: | 10.1007/s00421-007-0601-x |
Popis: | Systemic hypoxia leads to peripheral vasodilation that serves to counteract the decrease in peripheral oxygen (O(2)) delivery. Skeletal muscle vasodilation associated with hypoxia is due to release of vasodilator substances such as adenosine and/or nitric oxide (NO). We hypothesized that skeletal muscle may act as a source of NO during exposure to hypoxia. Therefore, we measured NO in forearm venous plasma and in skeletal muscle interstitial dialysate in seven healthy young men during exposure to simulated altitude of 2,438 and 4,877 m (20 min at each level) in a hypobaric chamber. O(2) saturation (mean +/- SEM) fell from 98.0 +/- 0.2% at ambient conditions to 91.0 +/- 0.4% at 2,438 m and to 73.2 +/- 4.4% at 4,877 m (P < 0.05). While blood pressure remained unchanged, heart rate increased in a graded fashion (P < 0.05). Plasma NO (chemiluminescence method) rose from 11.6 +/- 1.3 to 16.9 +/- 2.9 microM at 2,438 m (P < 0.05) but remained similar at 16.4 +/- 2.3 microM at 4,877 m (NS). In contrast, skeletal muscle microdialysate NO levels were lower than plasma NO (P < 0.01) and did not change during simulated altitude. Thus, hypoxia produced by simulated high altitude exposure leads to an increase in plasma but not skeletal muscle interstitial NO. These data support an important role of NO in the peripheral vascular responses to hypoxia. The differential responses of plasma vs. interstitial NO during hypoxia suggest an endothelial or intravascular source of NO. |
Databáze: | OpenAIRE |
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