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Am J Physiol Heart Circ Physiol (December 11, 2003). doi:10.1152/ajpheart.00120.2003
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Submitted on February 6, 2003
Accepted on December 10, 2003

Pattern differences between distributions of microregional myocardial flows in crystalloid- and blood-perfused rat hearts

Takeshi Matsumoto1*, Hiroyuki Tachibana2, Takahisa Asano2, Mami Takemoto2, Yasuo Ogasawara2, Keiji Umetani3, and Fumihiko Kajiya4

1 Department of Medical Engineering and Systems Cardiology, Kawasaki Medical School, Kurashiki, Okayama, Japan; Department of Mechanical Science and Bioengineering, Osaka University Graduate School of Engineering Science, Toyonaka, Osaka, Japan
2 Department of Medical Engineering and Systems Cardiology, Kawasaki Medical School, Kurashiki, Okayama, Japan
3 Life and Environmental Science Division, Japan Synchrotron Radiation Research Institute, Mikazuki, Hyogo, Japan
4 Department of Medical Engineering and Systems Cardiology, Kawasaki Medical School, Kurashiki, Okayama, Japan; Department of Cardiovascular Physiology, Okayama University Graduate School of Medicine and Dentistry, Okayama, Okayama, Japan

* To whom correspondence should be addressed. E-mail: matsumoto{at}me.kawasaki-m.ac.jp.

Regional myocardial flow distributions in Langendorff rat hearts under Tyrode and blood perfusion were assessed by digitalradiography (100-µm resolution) using tritiated desmethylimipramine as a molecular flow tracer. Spatial patterns of flow distribution during baseline and maximal hyperemia following a 60-sec flow cessation were evaluated by the coefficient of variation of regional flows (CV, related to global flow heterogeneity) and the correlation between adjacent regional flows (CA, inversely related to local flow randomness). These values were obtained for the original images (642 pixels) and for coarse-grained images (322, 162, and 82 blocks of nearby pixels, i.e., pixel aggregates). At a given point in time during baseline, both CV and CA were higher in blood (n=7) than in Tyrode perfusion (n=7) over all pixel aggregates (P<0.05, two-way ANOVA). During the maximal hyperemia, CV and CA were still significantly higher in blood (n=7) than in Tyrode perfusion (n=7); however, these values decreased substantially in blood perfusion and the CV- and CA-differences became smaller than those at baseline accordingly. During basal blood perfusion, the 60-sec averaged flow distribution (n=7) showed the smaller CV and CA than those at a given point in time (P<0.05, two-way ANOVA). Coronary flow reserve was significantly higher in blood than in Tyrode perfusion. In conclusion, the flow heterogeneity and the local flow similarity are both higher in blood than in Tyrode perfusion, probably due to both the different degree of coronary tone preservation and the presence or absence of blood corpuscles. Under blood perfusion, temporal flow fluctuations for short-term periods of 60-sec order are largely involved in shaping microregional flow distributions.




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