2012
DOI: 10.1111/j.1549-8719.2012.00165.x
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A Simple “Streak Length Method” for Quantifying and Characterizing Red Blood Cell Velocity Profiles and Blood Flow in Rat Skeletal Muscle Arterioles

Abstract: We present a means for quantifying blood flow in continuously branching skeletal muscle arterioles. Further, we provide an equation for calculating velocity ratios based on arteriolar diameter, which may be used by others for blood flow calculations.

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Cited by 25 publications
(55 citation statements)
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“…Centerline RBC velocities were acquired by taking multiple centerline streak length (camera exposure: 10 -20 ms depending on RBC velocity) measurements using ImageJ software (manual; ImageJ 1.43 u; National Institutes of Health, Bethesda, MD). Mean RBC velocity was calculated by correcting centerline streak lengths with a velocity ratio factor (Vratio) previously determined based on the arteriolar diameter of interest, where Vratio ϭ (0.0071 ϫ diameter) ϩ 1.15 (1). Blood flow was calculated as a product of mean RBC velocity and vessel cross-sectional area.…”
Section: Rat Gluteus Maximus Skeletal Muscle Modelmentioning
confidence: 99%
“…Centerline RBC velocities were acquired by taking multiple centerline streak length (camera exposure: 10 -20 ms depending on RBC velocity) measurements using ImageJ software (manual; ImageJ 1.43 u; National Institutes of Health, Bethesda, MD). Mean RBC velocity was calculated by correcting centerline streak lengths with a velocity ratio factor (Vratio) previously determined based on the arteriolar diameter of interest, where Vratio ϭ (0.0071 ϫ diameter) ϩ 1.15 (1). Blood flow was calculated as a product of mean RBC velocity and vessel cross-sectional area.…”
Section: Rat Gluteus Maximus Skeletal Muscle Modelmentioning
confidence: 99%
“…This stands in contrast to the bulk perfusion measurements acquired by laser Doppler perfusion imaging (9, 18, 43) and wide field applications of LSF (7, 18, 38). Second, where high resolution is available, such as in the recent development of optical imaging techniques including optical coherent tomography (13, 50), intravital microscopy of fluorescent particles (1, 30, 42), and multiphoton microscopy (24, 26), there are often limitations with respect to spatial coverage and the challenges of registering multiple fields of view. A similar difficulty is present in the more traditional microvascular tools of autocorrelation and dual-slit velocimeters (8, 46) in the experimental duration needed to capture hemodynamics throughout an entire network one vessel at a time.…”
Section: Discussionmentioning
confidence: 99%
“…The animal preparation and IVVM techniques used are described in detail in Ref. . Also described in Ref.…”
Section: Experimental Methodsmentioning
confidence: 99%