Validation of the vesicular acetylcholine transporter (VAChT) and the neuro
nal vesicular monoamine transporter (VMAT2) as important molecular targets
in the cholinergic and dopamine neurons, respectively, has sparked interest
in the development of radiotracers for studying these markers in vitro and
in vivo. Currently, a number of selective high-affinity radiotracers are a
vailable for studying these targets in vivo with positron emission tomograp
hy (PET) or single photon emission computed tomography (SPECT), PET studies
of VMAT2 in neuropathology reveal changes in the density of this marker th
at can be verified independently. Similarly, in vivo studies with VAChT lig
ands suggest that the latter are potentially useful in detecting cholinergi
c lesions in vivo; however, additional development is required to fully rea
lize the potential of these radioligands.