
pmid: 1412517
The mechanism by which hypolipidemic drugs and industrial plasticizers cause hepatic tumors in rodents remains unknown. Protein kinase C is elevated during hepatic cell turnover, and sustained cellular replication has been shown to correlate with an increase in hepatic tumors. Therefore, the effect of [4-chloro-6-(2,3-xylidino)-2-pyrimidinylthio]acetic acid (Wy-14,643) on protein kinase C activity was examined. Female Sprague-Dawley rats were given 100 mg/kg Wy-14,643 in olive oil (i.g.), while control rats received equal volumes of oil vehicle. After 24 h, the activity of protein kinase C was estimated in isolated hepatic fractions by measuring the binding of 3H-phorbol-12,13-dibutyrate, a specific ligand for protein kinase C. Administration of Wy-14,643 significantly increased protein kinase C activity nearly 2-fold in microsomal fractions. Thus, it is possible that Wy-14,643 increases cell proliferation and causes tumors by mechanisms involving protein kinase C.
Anticholesteremic Agents, Administration, Oral, Rats, Enzyme Activation, Rats, Sprague-Dawley, Pyrimidines, Microsomes, Liver, Animals, Female, Protein Kinase C
Anticholesteremic Agents, Administration, Oral, Rats, Enzyme Activation, Rats, Sprague-Dawley, Pyrimidines, Microsomes, Liver, Animals, Female, Protein Kinase C
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