Driessen G, Rütten W, Inhoffen W, Scheidt H, Heidtmann H
Institut für Physiologie der RWTH Aachen, FRG.
Int J Microcirc Clin Exp. 1990 May;9(2):141-61.
To assess oxygen transport as a function of hematocrit, microcirculatory red blood cell flux (microflux) was measured by laser Doppler flowmetry (LDF) in the isolated rat mesentery as well as in cat sartorius muscle. The hematocrit value was varied from 0.5 to 50% while the perfusion pressure ranged from about 2.7 to 13 kPa. Simultaneously macroflux which is the volume flow times the systemic hematocrit value was determined. The curves LDF versus pressure showed saturation at several hematocrit values conveying the impression of autoregulation of microflux. The macroflux curves, on the other hand, curved upward. To clarify whether this discrepancy had a physiological cause, pressure-microflux as well as pressure-macroflux curves were collected in a flow chamber model where regulatory effects are absent. In the model the same discrepancies between micro- and macroflux as in vivo were observed. These discrepancies are explained by maximum values in velocity of about 3 mm/s and in hematocrit value of less than or equal to 20% which the LDF can discern. The limit in velocity is explained by the low pass filter of 12 kHz of the LDF instrument, the limit in hematocrit measurement is probably caused by the light scattering properties of red blood cell suspensions. A complicated combination of effects appears to be responsible for the linearity of the LDF signal versus macroflux at normal hematocrit value.
为了评估氧运输作为血细胞比容的函数,通过激光多普勒血流仪(LDF)在离体大鼠肠系膜以及猫的缝匠肌中测量了微循环红细胞通量(微通量)。血细胞比容值在0.5%至50%之间变化,而灌注压力范围约为2.7至13 kPa。同时测定了宏观通量,即体积流量乘以全身血细胞比容值。LDF与压力的曲线在几个血细胞比容值处显示出饱和,给人一种微通量自动调节的印象。另一方面,宏观通量曲线向上弯曲。为了阐明这种差异是否有生理原因,在一个不存在调节作用的流动腔模型中收集了压力-微通量以及压力-宏观通量曲线。在该模型中观察到与体内相同的微通量和宏观通量之间的差异。这些差异可以通过LDF能够识别的约3 mm/s的最大速度值和小于或等于20%的血细胞比容值来解释。速度限制是由LDF仪器的12 kHz低通滤波器解释的,血细胞比容测量的限制可能是由红细胞悬液的光散射特性引起的。在正常血细胞比容值下,LDF信号与宏观通量的线性关系似乎是由多种复杂效应共同作用导致的。