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Biomedical subjects

W Rütten

Publications and source records attributed to W Rütten.

7 recordsLinked to original sources

Active and passive modulation of cutaneous red cell flux as measured by laser Doppler anemometry.

1) We have found that the fluctuations in blood motion and blood content in cutaneous microvessels in man can be related to either active vasomotion (an order parameter for this system) or to a passive penetration of arterial (or venous, not shown) pressure waves (the control parameters for the microvascular blood motion). Arterial, respiratory (not shown), neuronal and myogenic rhythms can be clearly differentiated. 2) Spectral analysis of the signal fluctuations of a LDA method (monitoring phasic shifts in blood velocity) in combination with a photoplethysmographic method (monitoring shifts in blood content) can be used to identify the "normal state". In normal human subjects, it is characterized by broad band synergetic liberty (a wide spectrum of rhythmic activities between 0.01 and 5 Hz). The spectrum readily responds to changes in thermoregulatory state and/or myogenic activation by positional changes of the extremity. 3) The spectral analysis of LDA and photoplethysmographic records of the volar finger reveals predominance of active vasoconstriction during heat conserving thermoregulatory reflexes (18 degrees C ambient), predominantly passive reactions are seen at 27 degrees C. At 21-24 degrees C ("thermoregulatory indifference temperature range"), a mixed reaction pattern is seen. 4) Functional or irreversible elimination of the activity of subsystems leads to the elimination of circumscript spectral bands and/or potentiation of others. The functional differentiation of active and passive components can be utilized in the future for differential diagnosis of vascular and nervous disease state on the basis of spectral shifts and/or spectral narrowing.

Blood Flow Velocity↗

[Computer simulation of the dynamics of the arterial system for various cardiovascular situations].

The simulation model describes the basic characteristics of the pulse in a wide range of arterial vessels. By comparison of simulated stenosis with photoplethysmographic registered curves of patients suffering from stenosis, it could be shown, that also pathologic hemodynamics can be adequately described. A new sight of dicrotic pulse generation was derived by the simulated removal of large arteries. This led to the hypothesis of decoupled, autonomous multiple reflections in the arteries of the arm, the leg and the head.

Arterial Occlusive Diseases↗

Is the laser Doppler flow signal a measure of microcirculatory cell flux?

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.

Animals↗