“…Furthermore, the dissociation between the RBC and plasma traces indicates a separation of the RBC and the plasma passages through the parenchymal microcirculation, which may be caused by plasma skimming and/or thoroughfare channels for RBC (Hasegawa et al, 1967;Hudetz et al, 1996;Safaeian et al, 2011). Although no significant differences in the RBC and plasma transit were observed for the appearance times in the present study, the disappearance times showed detectable differences.…”
Section: Implication For Flow Regulatory Mechanisms In the Parenchymacontrasting
“…Furthermore, the dissociation between the RBC and plasma traces indicates a separation of the RBC and the plasma passages through the parenchymal microcirculation, which may be caused by plasma skimming and/or thoroughfare channels for RBC (Hasegawa et al, 1967;Hudetz et al, 1996;Safaeian et al, 2011). Although no significant differences in the RBC and plasma transit were observed for the appearance times in the present study, the disappearance times showed detectable differences.…”
Section: Implication For Flow Regulatory Mechanisms In the Parenchymacontrasting
“…36 In contrast, the capillary networks located in the RGCL/sIPL and dIPL/sINL demonstrated a tortuous, 3-D architecture that resembled the Voronoi tessellation described in cortical capillary beds. 37 The variation in retinal capillary network morphology identified in the present study demonstrates important parallels to the human cerebral cortex, where the microcirculation is also altered according to neuronal layer. [38][39][40] Unlike the brain, the retina is readily accessible for investigating the physiological behavior of subcellular components within distinct neuronal layers.…”
Section: Capillary Density Varies Between Retinal Layers and Ismentioning
Capillary networks in the human perifovea are morphometrically heterogeneous. Morphometric features of regional capillary networks in the layered retina may serve a critical role in supporting neuronal homeostasis. Improved knowledge of these features may be important for understanding pathogenic mechanisms underlying retinal vascular diseases.
“…Morphological and hemodynamic parameters are calculated for the entire tumor vasculature and various regions of interest (ROI) of the tumor (Safaeian et al, 2010). These include:
Eq.…”
Induction of tumor angiogenesis is among the hallmarks of cancer and a driver of metastatic cascade initiation. Recent advances in high-resolution imaging enable highly detailed three-dimensional geometrical representation of the whole-tumor microvascular architecture. This enormous increase in complexity of image-based data necessitates the application of informatics methods for the analysis, mining and reconstruction of these spatial graph data structures. We present a novel methodology that combines ex-vivo high-resolution micro-computed tomography imaging data with a bioimage informatics algorithm to track and reconstruct the whole-tumor vasculature of a human breast cancer model. The reconstructed tumor vascular network is used as an input of a computational model that estimates blood flow in each segment of the tumor microvascular network. This formulation involves a well-established biophysical model and an optimization algorithm that ensures mass balance and detailed monitoring of all the vessels that feed and drain blood from the tumor microvascular network. Perfusion maps for the whole-tumor microvascular network are computed. Morphological and hemodynamic indices from different regions are compared to infer their role in overall tumor perfusion.
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