PubMed · 1977 · 16 citations · 23 references
HepatologyBiochemistryMedicineLiver PhysiologyHyperplastic Liver LesionsHistopathologyPreneoplastic LiverPathologyToxicologyHyperplastic FociHepatotoxicityExperimental ToxicologyMetabolismPharmacologyRedox Biology3,3'-Diaminobenzidine ReactionToxicological MechanismOxidative Stress
Histochemical investigations used the 3,3'-diaminobenzidine reaction to demonstrate the catalase activity and thus variations in numbers of peroxisomes, and electron microscopic examinations were made of hyperplastic liver lesions in rats fed 0.06%3'-methyl-4-dimethylaminoazobenzene. At the 10th week of carcinogen feeding, hyperplastic lesions (hyperplastic foci, areas, and nodules) appeared and advanced to further stages. Most of the foci and some of the areas and nodules showed very low catalase activity and, correspondingly, a small number of peroxisomes. When rats were administered ethyl-alpha-p-chlorophenoxyisobutyrate, most of the foci, areas, and nodules showed a moderate increase in catalase activity and in peroxisome number. Hyperplastic foci seemed to grow larger with time to form hyperplastic areas and/or nodules, mostly accompanying maturation as well as proliferation of the hepatocytes involved. Maturation is well characterized by an increase in the endogenous level of catalase and in the number of peroxisomes, as well as by an enhancement of the responsiveness to ethyl-alpha-p-chlorophenoxyisobutyrate. However, there was a small proportion of lesions in which all cells or some cells did not mature and thus were considered persistently altered. It is suggested that these altered cells serve mainly as intimate precursors of hepatomas.
23
MICROBODIES IN EXPERIMENTALLY ALTERED CELLS
Donald J. Svoboda, Harold Grady, Daniel L. Azarnoff · The Journal of Cell Biology · 1967 · 231 citations · Full text
Sheldon M. Epstein, Nobuyuki Ito, Leonard P. Merkow et al. · PubMed · 1967 · 195 citations
J. M. Price, John W. Harman, E. C. Miller et al. · PubMed · 1952 · 170 citations