Positron emission tomography (PET) is one type of nuclear imaging that utilises
short-lived positron-emitting isotopes to allow visualisation and quantification
of biological processes or drug kinetics. Positron-emitting isotopes such
as [15O] (t1/2=2 min), [11C] (t1/2=20
min), [18F] (t1/2=109 min), [124I] (t1/2=
4.2 days) can be incorporated into many compounds of biological interest
to produce a radiotracer/radioligandsuch as [18F] fluorodeoxyglucose,
[11C] raclopride and [15O]H2O for PET studies.
A PET study begins with the injection or inhalation of a radiotracer followed
by scanning. When the radiotracer decays, it emits a positron that travels
a short distance and annihilates with an electron. Annihilation produces
two 511 keV photons, which propagate in nearly opposite directions and can
be detected within a short time window (the coincidence time window; ~10
ns). Many such events are summed to provide the distribution of the radiotracer.
Radiotracer transport, washout and retention can be monitored by PET; if
calibrated, PET images can yield quantitative estimates of the amount of
radiotracer in specific parts of the body. Additional information of blood
radioactivity levels or radioactivity in 'reference regions' enable calculation
of exchange rate constants/parameters such as receptor binding potential
that correlate with various physiological or pharmacological processes.
Application of PET to Study Biology of Small Animals
New developments in detector technologies have led to the commercialisation
of dedicated small animal scanners. It is now possible to perform PET studies
in animal models, thus, bridging the gap between in vitro science
and clinical studies. The potential of this technology to study biology
is huge and we are only beginning to realise this. Several of the radiotracers
employed clinically can be used to study the biology of animal models
and effects of therapy. In addition the PET is well suited to in vivo
functional genomic studies. Application in each setting (transgenics, tumour
models, lesioned rodents) requires a level of ex vivo validation
to appreciate the relationship between the PET imaging parameter and ex
vivo biochemistry/genetics.