Abstract
No single test gave unequivocal evidence of liver damage for all three compounds, the conventional liver function tests, alanine transaminase, aspartate transaminase, and alkaline phosphatase, whose plasma activities are usually reported in toxicity studies, were not the most sensitive indicators of the minimal liver cell damage caused by the drugs used in this experiment, knowledge of the intracellular location of the diagnostic enzyme makes it possible to describe, at least in part, the nature of the changes within the liver, measurement of plasma cholesterol and triglyceride levels can provide information about disruption in lipid metabolism, the times at which blood samples are taken are most important if transient drug effects on the liver are to be detected.