As the smallest arterioles are within this size range, they may also be undetectable. Thus, when the number of vessel

segments is plotted versus vessel diameter the curve has an inflection point, or “drops off” at the limit of detectability and essentially deletes small arterioles and capillaries from the segmented dataset (Figure 4C) [35]. This effect was well illustrated in the segmented rat liver vasculature, where a clear shift in this inflection point was shown when image resolution was increased [8]. The effect of image resolution on CHIR-99021 chemical structure arteriole detectability has also been observed in the mouse placenta [35], as well as in the rodent lung [43] and kidney [40]. Importantly, micro-CT measurements can be used to calculate a number of physiologically relevant variables given that blood flow rates through the fetoplacental arterial tree are low enough that a highly simplified pipe model is adequate to model blood flow [43]. In

this way, the distribution of pressures, flow rates, and wall shear stresses within each vessel segment, Endocrinology antagonist as well as the total arterial vascular resistance can be calculated [36, 43]. Micro-CT analysis of the fetoplacental tree in mice has been used to generate quantitative information, which has been statistically evaluated to determine changes during development, and caused by environmental or genetic abnormalities. The fetoplacental arterial tree in mice is supplied by a single umbilical artery, which branches into chorionic arteries localized at the fetal surface of the placenta within the chorionic plate [37, 1]. From these superficial arteries, the fetoplacental arteries branch and delve deeply into the labyrinthine exchange region traversing to the distal surface, near the relatively avascular junctional zone (Figure 5A) [37, 1]. At this point, the arterial tree supplies a mass of interconnecting capillaries (Figure 5A) that extend back toward the chorionic surface where the collecting veins are located [1]. The labyrinthine exchange Aprepitant region is also perfused by maternal blood, which passes through

a sponge-like network of fine sinusoids that give the labyrinth its name. The sinusoids receive maternal blood from maternal arterial canals, which in turn are supplied by spiral arteries located in the decidua (the maternal portion of the placenta) and the uterine artery (Figure 5B) [1]. Perfusion of the fetoplacental arterial tree begins at ~gd 9.5, when Doppler blood velocity is first routinely detected in the umbilical artery [30, 33]. Fetal growth is accompanied by progressive increases in umbilical artery diameter [37] and umbilical artery blood velocity from gd 9.5 to term (gd 18.5) [30, 33]. Micro-CT analysis shows that elaboration of the fetoplacental arterial tree is nearly complete by gd 13.