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Am J Physiol Heart Circ Physiol (January 9, 2003). doi:10.1152/ajpheart.00741.2002
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Submitted on August 26, 2002
Accepted on December 30, 2002

A New Method for Assessing Arteriolar Diameter and Hemodynamic Resistance Using Image Analysis of Vessel Lumen

Karel Tyml1*, Donald Anderson2, Darcy Lidington1, and Hanif M. Ladak3

1 A.C. Burton Laboratory, Lawson Research Institute, London, Ontario, Canada; Department of Medical Biophysics, University of Western Ontario, London, Ontario, Canada
2 Department of Medical Biophysics, University of Western Ontario, London, Ontario, Canada
3 Imaging Research Labs, Robarts Research Institute, London, Ontario, Canada; Department of Medical Biophysics, University of Western Ontario, London, Ontario, Canada; Electrical and Computer Engineering, University of Western Ontario, London, Ontario, Canada

* To whom correspondence should be addressed. E-mail: ktyml{at}lhsc.on.ca.

To characterize blood vessel's non-uniform diameter response to a given stimulus (e.g., arteriolar conducted response), frequent, serial diameter measurements along the vessel length are required. We used an advanced image analysis algorithm (i.e., the "discrete dynamic contour") to develop a quick and reliable method for serial luminal diameter measurements along the arteriole visualized by intravital video microscopy. Using digitized image of the arteriole and computer graphics, the method required an operator to mark the image of the two inner edges of the arteriole at several places along the arteriolar length. The algorithm then "filled in" these marks to generate two continuous contours that "hugged" these edges. A computer routine used these contours to determine luminal diameters every 20 µm. Based on these diameters and on the Poiseuille's law, the routine also estimated the hemodynamic resistance of the blood vessel. To demonstrate the usefulness of the method, we examined the character of spatial decay of KCl-induced conducted constriction along ~500 µm long arteriolar segments, and the KCl-induced increase in hemodynamic resistance computed for these segments. The decay was only modestly fitted by a simple exponential, while the computed increase in resistance (i.e., 5 to 70 fold) was only modestly predicted by resistance increase based on our mathematical model involving measurements at two arteriolar sites (Tyml et al., Am J Physiol 281: H1397-H1406, 2001). We conclude that our method provides quick and reliable serial diameter measurements. Since the change in hemodynamic resistance could serve as a sensitive index of conducted response, employment of this index in studies of conducted response may lead to new mechanistic insights of the response.




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