Our previous solution studies of the proton relaxation properties of g
lycogen H1 have shown significant dipolar cross-relaxation with intra-
ring H2 and inter-ring H4' protons characterized by a correlation time
tau(c) = 2.7 x 10(-9) s. This leads to a significant negative Nuclear
Overhauser Enhancement (NOE) of glycogen H1 following either transien
t or steady state perturbations of the longitudinal magnetization of d
ipolar coupled protons, especially H2 and H4'. Here we use the NOE to
edit selectively the H1 resonance of glycogen in the rat liver in vivo
using a surface coil probe. The approach shows the possibility of mea
suring glycogen in vivo with high sensitivity using H-1 NMR.