The relations between the urinary excretion of acid-soluble peptide (ASP)-form amino acids, the rate of whole body protein synthesis and plasma immunoreactive insulin-like growth factor-1 /somatomedin C concentration were investigated in rats. The urinary ASP-form leucine plus valine excretion correlated well with the rate of whole body protein synthesis and with the plasma immunoreactive insulin-like growth factor-1 concentration. The results provide further evidence for the hypothesis that urinary excretion of ASP is an excellent index of the status of protein metabolism in animals.Insulin-like growth factor-1 : Protein synthesis : Acid-soluble peptides : Rat Previously we reported that the urinary excretion of acid-soluble peptides (ASP) is potentially an excellent index of whole body protein degradation (Noguchi et a/. 1982(Noguchi et a/. , 1988. Based on observations of the relationship between urinary excretion of ASP and total nitrogen under various nutritional conditions, we proposed a hypothesis for the assessment of protein metabolism. The hypothesis contained two assumptions : the first was that urinary excretion of ASP is proportional to the rate of whole body protein degradation, the second was that the ratio of urinary N: ASP is linearly correlated with the efficiency of dietary N utilization at the recommended requirement level of dietary protein.(i.e. If the dietary protein level exceeded the recommended level, the ratio increased according to the increase in dietary protein content, even in the rats fed on the casein diets.) It has been shown by several authors that the fractional rate of tissue (for example, muscle) or whole body protein synthesis (or fractional rate of tissue growth or protein gain) is positively correlated with the fractional rate of their protein degradation (i.e. tissues which are actively synthesizing their proteins also degrade their proteins actively) if animals are not suffering from special degenerative diseases or are not given drugs such as glucocorticoid or thyroid hormones (Millward et a/.