Rats were injected with Se 75 -sodium selenite, Se75-sodium selenate, and Se75-selenomethionine, and the distributions of Se75 in tissues, and in proteins isolated from plasma, liver supernatants, and kidney supernatants, were studied as a function of time.The livers of rats injected with selenite had a much greater initial Se75 concentration than those from rats receiving selenate. Kidneys of rats injected with selenite had a peak Se 75 concentration in the sample taken 1 hr after injection; this was followed by a rapid decline. Kidneys from rats injected with selenate had an almost constant Se75 level in all samples from 1 hr to 7 days. In other tissues the Se 75 activities for rats injected with selenite were similar to those for rats injected with selenate. As has been reported elsewhere the tissues retaining the highest Se 75 levels were the livers, kidneys, and adrenals.Rats injected with selenomethionine contained greater Se 75 concentrations in the pancreas than rats injected with selenite or selenate.Dialysis of plasma and liver and kidney supernatants against isotonic saline showed that at I hr after injection selenomethionine was associated with protein to a greater extent than was selenite or selenate. Disulphide-cleaving reagents (mercaptoethanol and cysteine) and urea were effective in releasing Se75 from liver, kidney, and plasma proteins from rats injected with either selenomethionine, selenite, or selenate. Se i ;, distribution patterns in liver. kidney, and plasma proteins separated by gel filtration or disc-electrophoresis were very similar for samples collected at I day, 3 days, and 7 days after injection of rats with either selenite, selenate, or selenomethionine. If, as has been rroposed, selenium from selenite or selenate is present in protein as selenotrisulphide, this finding suggests that selenomethionine may not be incorporated into protein intact.115