Maxwell L C, Shepherd A P, McMahan C A
Am J Physiol. 1985 Feb;248(2 Pt 2):H217-24. doi: 10.1152/ajpheart.1985.248.2.H217.
Significant quantities of 9-micron microspheres (20-30%) are not trapped in the intestine following intracardiac or intra-arterial injection, but reach venous blood. Some investigators propose that the passage of 9-micron spheres measures blood flow through noncapillary connections. Because frequency distributions of intestinal capillary diameters and 9-micron spheres overlap, microspheres could simply pass through capillaries. Therefore, we developed simple probabilistic models to predict both the size distribution and the percentage of injected spheres [9 +/- 1 (SD) micron] that should appear in venous blood. Chief assumptions in models are that microsphere delivery and sphere diameter are independent and that microspheres pass through capillaries of equal or larger size. The passage predicted by the models was consistent with values in canine intestinal circulation, demonstrating that passage through capillaries [7.38 +/- 1.4 (SD) micron] adequately accounts for spheres in venous blood. Because the diameters of nominal 9-micron spheres were distributed too narrowly to show a marked sieving effect on passage through the intestinal circulation, we also injected microspheres varying from 5 to 20 micron in diameter. This mixture demonstrated a marked sieving effect. The predicted frequency distribution for microsphere diameters in venous blood agreed with the observed distribution. Our models demonstrate that the passage of 9-micron spheres through capillaries, rather than through "shunts," adequately accounts for the appearance of spheres in venous blood and suggests that the frequency distribution of venous microspheres can provide an in vivo method for estimating the frequency distribution of intestinal capillary diameters.
心内或动脉内注射后,大量9微米的微球(20%-30%)未被肠道捕获,而是进入静脉血。一些研究者提出,9微米微球的通过可测量非毛细血管连接的血流。由于肠道毛细血管直径和9微米微球的频率分布重叠,微球可能只是简单地穿过毛细血管。因此,我们建立了简单的概率模型来预测静脉血中注射微球[9±1(标准差)微米]的大小分布和百分比。模型的主要假设是微球传递和球直径是独立的,且微球穿过大小相等或更大的毛细血管。模型预测的通过情况与犬肠道循环中的值一致,表明通过毛细血管[7.38±1.4(标准差)微米]足以解释静脉血中的微球。由于标称9微米微球的直径分布过窄,无法显示出对通过肠道循环的明显筛分效应,我们还注射了直径从5到20微米不等的微球。这种混合物显示出明显的筛分效应。静脉血中微球直径的预测频率分布与观察到的分布一致。我们的模型表明,9微米微球通过毛细血管而非“分流”,足以解释静脉血中微球的出现,并表明静脉微球的频率分布可为估计肠道毛细血管直径的频率分布提供一种体内方法。