Literature DB >> 8321143

Interpretation of the laser Doppler flow signal from the liver of the rat.

A M Wheatley1, N E Almond, E T Stuart, D Zhao.   

Abstract

It has been proposed that the laser Doppler flow (LDF) signal from the surface of the rat liver is almost exclusively a measure of hepatic arterial and not of total liver blood flow and therefore that LDF is not a suitable technique for the measurement of blood flow in the hepatic microcirculation. The objective of the present study was twofold: (i) to establish that liver blood flow is homogeneously distributed and (ii) to assess the behavior of the LDF signal during changes in hepatic perfusion. When 51Cr-labeled microspheres were injected into the portal vein (n = 12), no significant differences in the relative flow (cpm/lobe to cpm/liver) to each of the liver lobes were found nor was there any difference in the ratio of flow to the outer 1-2 mm of lobe as compared to that to the "core" of the liver. Temporary occlusion of the hepatic artery and the portal vein caused approximately 13% (n = 7, P < 0.001) and approximately 74% (n = 7, P < 0.001) fall in LDF signal, respectively. Diversion of flow from the anterior to the posterior lobes (n = 5) caused a 97.9 +/- 21.1% (SD, P < 0.001) rise in LDF signal in the posterior lobes. Zero-flow LDF signal was found to represent 13.0 +/- 4.1% of maximum. Hemorrhage (in 1.5-ml aliquots) was associated with a fall in mean arterial pressure (MAP) and LDF signals. A linear relationship between MAP and the LDF signal (r > 0.9) was found. Reinfusion of blood caused both MAP and the LDF signal to return to normal. We conclude that (i) blood flow in rat liver is homogeneously distributed; (ii) the LDF signal from the liver surface responds in a manner predicted by conventional theories of hepatic hemodynamics during alteration, either independent or combined, in hepatic arterial and portal venous blood flow; and (iii) LDF may be used to measure relative changes in hepatic perfusion but problems associated with zero-flow signal and intersite variability preclude its quantification in absolute flow units.

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Year:  1993        PMID: 8321143     DOI: 10.1006/mvre.1993.1025

Source DB:  PubMed          Journal:  Microvasc Res        ISSN: 0026-2862            Impact factor:   3.514


  5 in total

1.  Age-related changes in the hepatic microcirculation in mice.

Authors:  Yoshiya Ito; Karen K Sørensen; Nancy W Bethea; Dmitri Svistounov; Margaret K McCuskey; Bård H Smedsrød; Robert S McCuskey
Journal:  Exp Gerontol       Date:  2007-04-29       Impact factor: 4.032

2.  A novel, microscope based, non-invasive laser Doppler flowmeter for choroidal blood flow assessment.

Authors:  C Strohmaier; R M Werkmeister; B Bogner; C Runge; F Schroedl; H Brandtner; W Radner; L Schmetterer; J W Kiel; G Grabner; H A Reitsamer
Journal:  Exp Eye Res       Date:  2011-04-01       Impact factor: 3.467

3.  Heterogeneous suppression of experimentally induced colon cancer metastasis in rat liver lobes by inhibition of extracellular cathepsin B.

Authors:  C J Van Noorden; T G Jonges; J Van Marle; E R Bissell; P Griffini; M Jans; J Snel; R E Smith
Journal:  Clin Exp Metastasis       Date:  1998-02       Impact factor: 5.150

4.  Laser speckle contrast imaging for intraoperative assessment of liver microcirculation: a clinical pilot study.

Authors:  Sam Eriksson; Jan Nilsson; Gert Lindell; Christian Sturesson
Journal:  Med Devices (Auckl)       Date:  2014-07-25

5.  Changes in tumour blood flow, oxygenation and interstitial fluid pressure induced by pentoxifylline.

Authors:  I Lee; Y Boucher; T J Demhartner; R K Jain
Journal:  Br J Cancer       Date:  1994-03       Impact factor: 7.640

  5 in total

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