The increasing use of thallium-201 (201Tl) in myocardial imaging studi
es during the last two decades, has justified a re-examination of the
metabolism of this metal compound. It was found that about 4% of an in
jected dose was rapidly distributed to the healthy human myocardium, w
hich is in agreement with previous reports. Apparent similarities exis
t between the transport of ionic thallium and potassium through cell m
embranes. Upon clinical use, myocardial perfusion scintigraphy is rout
inely carried out after iv administration of the agent. It is generall
y accepted that the rapid myocardial extraction of circulating Tl-201,
during the initial 30 min, depends upon an unimpaired blood perfusion
; whereas the prolonged uptake/redistribution during the next 3 h refl
ects myocardial viability. In the present paper, the reliability of Tl
-201 scintigraphy to disclose insufficient myocardial perfusion is ill
ustrated by the examination of biological samples from patients, that
were also studied by the classical coronary angiographic technique, th
e two methods showed an acceptable degree of agreement.