Purpose: Our goal was to demonstrate the feasibility of an in vivo noninvas
ive method for imaging spinal cord cholinergic terminals using (+)-4-[F-18]
fluorobenzyltrozamicol ([F-18]FBT) and PET.
Method: In vitro and in vivo experiments in rats were conducted to demonstr
ate the specific binding characteristics, localization, and time course of
[H-3]FBT binding in the spinal cord. PET imaging was then performed on seve
n rhesus monkeys.
Results: The rat studies demonstrate high specific binding in the spinal co
rd with a distribution coinciding with the known distribution of cholinergi
c terminals. In vivo tracer concentrations in the spinal cord and basal gan
glia were of the same magnitude. With use of [F-18]FBT and PET in the rhesu
s monkey, the spinal cord was clearly visualized, with tracer concentration
in the spinal cord being approximately one-fourth of that seen in the basa
l ganglia.
Conclusion: This work demonstrates the feasibility of imaging cholinergic t
erminals in vivo in the spinal cord using [F-18]FBT and PET.