“…The radioactivity of the applied labeled precursor would be diluted by acetyl-CoA through glycogen degradation. This last assumption is supported by the following facts: first, in vivo, the inhibitory effect appears only in liver and not in the carcass or in adipose tissue with cAMP or its dibutyryl derivative [3] or with cGMP [4] ; second, the two successive administrations of db cAMP failed to inhibit the liver fatty acid synthesis in vivo. Thus when the animals have been deprived of glycogen by a first injection of db cAMP, the inhibitory effect of this compound disappears.…”