Neurosci Behav Physiol
Tissue Gas Exchange Physiology Group, I. P. Pavlov Institute of Physiology, Russian Academy of Sciences, 6 Makarov Bank, 199034, St. Petersburg, Russia.
Published: May 2009
Modified needle oxygen microelectrodes and vital microscopy were used to measure transmural oxygen tension gradients (PO2) in pial arterioles with lumen diameters of 20-90 microm. A relationship between the magnitude of the transmural PO2 gradient and arteriole wall tone was found: in control conditions, PO2 gradients were 1.17 +/- 0.06 mmHg/microm (n = 40), while in conditions of arteriolar wall dilation the transmural PO2 gradient decreased to 0.68 +/- 0.04 mmHg/microm (p < 0.001, n = 38). These data provide the first measurements of transmural PO2 gradients in pial arterioles of different calibers at different levels of vascular tone and have fundamental importance for assessing the role of arterial microvessels in tissue oxygen supply processes. The results obtained here provide evidence that oxygen consumption by the vessel wall is within the range characteristic of enveloping tissues and that oxygen consumption by the endothelial cell layer probably has no significant effect on the magnitude of the transmural PO2 gradient.
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http://dx.doi.org/10.1007/s11055-009-9142-6 | DOI Listing |
J Physiol
August 2020
Department of Kinesiology, Kansas State University Manhattan, KS.
Key Points: Within skeletal muscle the greatest resistance to oxygen transport is thought to reside across the short distance at the red blood cell-myocyte interface. These structures generate a significant transmural oxygen pressure (PO ) gradient in mixed fibre-type muscle. Increasing O flux across the capillary wall during exercise depends on: (i) the transmural O pressure gradient, which is maintained in mixed-fibre muscle, and/or (ii) elevating diffusing properties between microvascular and interstitial compartments resulting, in part, from microvascular haemodynamics and red blood cell distribution.
View Article and Find Full Text PDFMicrocirculation
July 2019
Departments of Anatomy & Physiology, Kinesiology, Kansas State University, Manhattan, Kansas.
The oxygen transport pathway from air to mitochondria involves a series of transfer steps within closely integrated systems (pulmonary, cardiovascular, and tissue metabolic). Small and finite O stores in most mammalian species require exquisitely controlled changes in O flux rates to support elevated ATP turnover. This is especially true for the contracting skeletal muscle where O requirements may increase two orders of magnitude above rest.
View Article and Find Full Text PDFJ Physiol
March 2018
Departments of Anatomy & Physiology, Kinesiology, Kansas State University, Manhattan, KS, USA.
Key Points: Oxygen pressure gradients across the microvascular walls are essential for oxygen diffusion from blood to tissue cells. At any given flux, the magnitude of these transmural gradients is proportional to the local resistance. The greatest resistance to oxygen transport into skeletal muscle is considered to reside in the short distance between red blood cells and myocytes.
View Article and Find Full Text PDFAm J Physiol Heart Circ Physiol
April 2018
Department of Biomedical Engineering, The George Washington University, Washington, District of Columbia.
The left ventricular working, crystalloid-perfused heart is used extensively to evaluate basic cardiac function, pathophysiology, and pharmacology. Crystalloid-perfused hearts may be limited by oxygen delivery, as adding oxygen carriers increases myoglobin oxygenation and improves myocardial function. However, whether decreased myoglobin oxygen saturation impacts oxidative phosphorylation (OxPhos) is unresolved, since myoglobin has a much lower affinity for oxygen than cytochrome c oxidase (COX).
View Article and Find Full Text PDFBasic Res Cardiol
November 2016
Division of Experimental Cardiology, Department of Cardiology, Thoraxcenter, Cardiovascular Research School COEUR, Erasmus University Medical Center, Rotterdam, The Netherlands.
Accelerated development of coronary atherosclerosis is a defining characteristic of familial hypercholesterolemia (FH). However, the recent data highlight a significant cardiovascular risk prior to the development of critical coronary stenosis. We, therefore, examined the hypothesis that FH produces coronary microvascular dysfunction and impairs coronary vascular control at rest and during exercise in a swine model of FH.
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