Friedman J J, Hing C T
Microvasc Res. 1985 Jul;30(1):45-55. doi: 10.1016/0026-2862(85)90036-6.
The effect of long-term (4 hr) intraarterial norepinephrine (NOR) infusion on vascular resistance (R), transcapillary fluid movement (Jv), and protein transport (Js) was determined in the isolated hindlimb of the dog. The limb was isolated by an occluding tourniquet and perfused at constant pressure with blood from the opposite femoral artery. Tissue volume changes were detected with a Whitney (1953) mercury-in-rubber strain gauge and protein transport assessed by direct monitoring of the rate of accumulation of 125I-albumin in the tissue. Periodically venous pressure (Pv) was elevated 20 mm Hg in order to estimate the capillary filtration coefficient (Kf) and to determine whether or not prolonged NOR exposure modified the microcirculatory response to increased pressure. Infusing NOR at a delivered dose ranging from 0.026 to 0.13 micrograms/ml significantly elevated R for the entire infusion period. Tissue volume and radioactivity declined transiently and then returned to the control level within 15 min and remained at this level for the remainder of the infusion period. These changes were attributed to blood volume shifts. Elevating Pv during NOR infusion further increased R to an extent which exceeded that during control. Jv and Js were elevated to a greater extent than during control with the delta Js exceeding delta Jv. The changes in Jv are probably due to an increase in microvascular surface area as reflected in an elevated Kf. The greater increase in Js is due in part to an increase in convective transport across a greater microvascular surface area. However, since the ratio of Js/Jv increased with Pv elevation following NOR, the increased Js may represent a change in microvascular permeability produced by the increased Pv. It is also possible that due to myogenic activity or a venous-arteriolar reflex, the microvascular pressure profile was shifted toward the venous side where the reflection coefficient is lower.
在犬离体后肢中,测定了长期(4小时)动脉内输注去甲肾上腺素(NOR)对血管阻力(R)、跨毛细血管液体移动(Jv)和蛋白质转运(Js)的影响。通过止血带阻断使后肢离体,并用对侧股动脉的血液在恒定压力下进行灌注。用惠特尼(1953年)的橡胶汞应变仪检测组织体积变化,并通过直接监测组织中125I-白蛋白的积累速率来评估蛋白质转运。为了估计毛细血管滤过系数(Kf)并确定长时间暴露于NOR是否会改变微循环对压力升高的反应,定期将静脉压(Pv)升高20 mmHg。以0.026至0.13微克/毫升的给药剂量输注NOR,在整个输注期间显著升高R。组织体积和放射性短暂下降,然后在15分钟内恢复到对照水平,并在输注期的剩余时间内保持在该水平。这些变化归因于血容量的改变。在输注NOR期间升高Pv会进一步使R升高,升高程度超过对照期间。Jv和Js的升高幅度大于对照期间,且ΔJs超过ΔJv。Jv的变化可能是由于微血管表面积增加,这反映在Kf升高上。Js的更大升高部分归因于对流运输在更大的微血管表面积上增加。然而,由于NOR后Js/Jv比值随Pv升高而增加,Js的增加可能代表Pv升高导致的微血管通透性变化。也有可能由于肌源性活动或静脉-小动脉反射,微血管压力分布向反射系数较低的静脉侧偏移。