Metabolic characteristics of colon mucosa, submucosa, muscularis and t
umour specimens from four control (n=105) and nine carcinogen (azoxyme
thane)-treated (n=91) Sprague-Dawley rats were investigated by ex vivo
H-1 MRS, Ninety-seven per cent of pure mucosa samples (n=59) yielded
spectra with narrow lipid resonances (chemical shift delta of -(CH2)(n
)-, 1.3 ppm; linewidth at half-height nu(1/2), 30-50 Hz), Eighty-two p
er cent of control mucosa samples with histologically proven submucosa
contamination (n=11) and 46% of control cross-sections (containing mu
cosa, submucosa and muscularis; n=57) yielded spectra with broad lipid
resonances (delta -(CH2)(n)-, 1.5 ppm; nu(1/2), 80-100 Hz) identical
to those of adipose tissue surrounding rat colon, Thirty per cent of t
umour samples (n=10) yielded spectra with narrow lipid resonances whil
e 70% contained no significant amount of MR visible lipids. We conclud
e that (i) lipids giving rise to broad resonances are in the heterogen
eously distributed adipocytes of submucosa, (ii) lipids giving rise to
narrow resonances are within the mucosa in an unknown structural envi
ronment, and (iii) the type and distribution of lipids in human and ra
t colon are similar, Tumours contained significantly more taurine than
pure control mucosa (n=15; p<0.004) and pure mucosa containing aberra
nt crypt foci (putative preneoplasm, n=36; p<0.002). Our results sugge
st that the rat colon is a good model for H-1 MR investigations of hum
an colon carcinogenesis.