Perfusion (blood flow)
Perfusion is the volume of blood flowing through certain mass (or volume) of tissue per unit time. Blood flow is usually given in units mL/(100 g * min) or mL/(mL * min).
Tissue perfusion can be measured noninvasively with positron emission tomography using the following general techniques:
- Clearance or uptake of an inert and diffusible tracer
- Equilibrium imaging of a short-lived, inert, and diffusible tracer
- Uptake of a labelled agent that is trapped in capillaries or diffusible tracer that is metabolically trapped in cells.
The methods to measure perfusion with diffusible and inert tracers are based on the principle of exchange of inert gas between blood and tissues (Kety and Schmidt, 1945; Kety, 1985), and on the Fick’s principle. External detection of radioactive 85Kr and 133Xe has been used to measure regional perfusion in the brain (Lassen & Ingvar, 1961; Ingvar & Lassen, 1962; Glass & Harper, 1963). 133Xe clearance method has been widely used, but it will only give an estimate of the total blood flow (both nutritive and non-nutritive), and is dependent on the tissue-blood -partition coefficient, which is dependent on the relative water and fat contents. The clearance methods were used also with [15O]H2O and [15O]O2 (Ter-Pogossian et al., 1969). Usage of short-lived isotopes allows perfusion measurement with equilibrium analysis during constant infusion (Huang et al., 1979). Kety model is not applicable to extracellular contrast media that are used in CT and MR imaging, but the model of Morales and Smith (1948) can be used instead (Brix et al., 1999).
Radiotracers that remain in vascular space cannot be used to measure blood flow (Lassen, 1984). Without an accurate deconvolution method with known local unit impulse residue function, at its best, such tracer can provide an estimate of plasma or blood volume in the tissue, which may vary in the same direction as the plasma flow, and thus appear to correlate with blood flow (Lassen, 1984). For instance, contrast agent based CT perfusion measurements provide variable results depending on the deconvolution method (Ibaraki et al., 2015).
The term blood flow commonly refers to the volume of blood passing through arteries and veins per unit time. Arterial bulk flow can end up in tissue capillaries (nutritive capillary blood flow), or flow into veins through shunts or arterio-venous anastomoses (nonnutritive blood flow). Depending on the blood flow measurement technique, and site of measurement, nutritive and nonnutritive flow may contribute to bulk blood flow with varied shares. For instance, indicator-dilution methods (Meier & Zierler, 1954) estimate the total blood flow. Blood perfusion refers to nutritive capillary blood flow.
When perfusion is measured using diffusible PET tracers, such as [15O]H2O, the nonnutritive (noneffective) fraction of blood flow (blood flowing through shunts is not included in the perfusion estimate. The fraction of nonnutritive flow is especially high the in the skin. By definition, in shunts arterial and venous blood concentrations are equal, Ca - Cv = 0, and thus it has no effect on the concentration in tissue, based on the Fick’s principle.
However, nonnutritive blood flow will increase the estimate of arterial blood volume, because both the arterial and venous fraction of the shunt volume will have the same kinetics.
Microspheres of different diameters can be used in animal studies to measure nutritive and nonnutritive blood flow.
Tissue perfusion has two conflicting effects on the uptake of the radiotracer: delivery of the tracer molecules is directly proportional to the perfusion, but, once delivered, chances of tissue extraction of the tracer molecule decreases with increasing perfusion. Depending on the relative rates of blood flow and transport, the effect of perfusion can range between two extremes: the uptake rate can be determined entirely by perfusion (perfusion-limited), or it can be essentially independent of perfusion and determined only by transport (Holden, 1985). Tracers that meet the first condition are perfect for measurement of perfusion, but useless for anything else. Most PET radiotracers are in the middle-ground. Capillary walls and endothelial cells can be very different in different organs. Blood-brain barrier limits the transport of most tracers, making the uptake less perfusion-dependent, but in another tissue the uptake may be perfusion-limited, and therefore useless for measuring any step beyond perfusion step. Uptake can be transport- or diffusion-limited at high blood flow, but perfusion-limited at low blood flow (Peters & Jamar, 1998).
- Fick’s principle
- Analysis instructions by tracer
- Dynamic processes
- Compartmental model
- Compartmental model for radiowater
- ARG method
- Vascular system
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Updated at: 2019-01-16
Created at: 2014-04-07
Written by: Vesa Oikonen