1) The enzymatic desamination of 13 homologous fatty acid amides and 2 ω-phenyl fatty acid amides in the liver extract of rats on hepatic carcinogens, 4-dimethylaminoazobenzene or 2-acetylaminofluorene, has been investigated.
2) Aqueous homogenate of normal liver had the marked activity to evolve ammonia from the above mentioned substrates, although the amount differed according to the sorts of substrates employed.
3) The pathological but non-cancerous liver showed the appropriate activity even in the case of marked alteration, as long as the neoplastic transformations had not taken place.
4) Hepatoma had very low activity, scarcely reaching about 1/4 to 1/30 that of normal liver according to the sorts of substrate employed.
5) So far as the straight chained fatty acid amides which could be used as aqueous solutions are concerned, the more easily they were cleaved by liver extracts the richer they are in carbon atoms, and the straight chained compounds were decomposed more readily than the branched with corresponding molecular weight.
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