A B S T R A C T After oral administration of [2,4-3H]-cholyl [S]taurine to eight healthy subjects with indwelling nasoduodenal tubes, the specific activity of the cholyl and taurine moieties and the distribution of radioactivity in biliary bile acid and urinary metabolites, as well as total urinary and fecal 'S and 'H, vere measured at intervals for 4-8 days. Similar measurements were made after ["S]taurine was given orally or intravenously or instilled into the distal intestine. The daily fractional turnover rate of the taurine moiety of cholyltaurine was low and similar to that of the cholyl moiety, indicating that deconjugation occurring during enterohepatic cycling was less than half that previously observed for glycine-conjugated bile acids. Some of the cholyl moiety was absorbed but, since reconjugation occurred predominantly with glycine, little reincorporation into the cholyltaurine pool was observed. Some of the taurine moiety was also absorbed intact but entered large taurine pools, and little reincorporation into the cholyltaurine pool was seen. Oral administration of taurine expanded the cholyltaurine pool and induced a decrease in the fractional turnover rate of the cholyl moiety of cholyltaurine, interpreted to indicate a greater reincorporation of the cholyl moiety because of increased reconjugation with taurine. Taurine moiety not absorbed as taurine appeared to be absorbed largely as sulfate which, like taurine, entered large endogenous pools. Little fecal excretion of 'S occurred. 'S was excreted in urine as taurine and sulfate, and excretion in the first 24 h (as per-
INTRODUCTIONWe have previously defined the metabolism of the steroid and amino acid moieties of glycine-conjugated bile acids (1, 2) in man. About 18% of the pool of glycineconjugated bile acids is deconjugated in each enterohepatic cycle and about two-thirds of the steroid moiety liberated is conserved and reconjugated, predominantly with glycine in the liver. Consequently, the synthesis of bile acid glycine is about three times that of the steroid moiety. The glycine liberated from cholyl[1-14C]glycine in the gastrointestinal tract is either converted to 4CO2 in the intestinal lumen or, if absorbed, enters the large body pool of glycine; virtually none of the glycine liberated in the intestinal lumen can be detected in the glycine used for conjugation with free bile acids in the liver.In man, about one-quarter of the biliary bile acids are conjugated with taurine (3). Garbutt, Wilkins, Lack, and Tyor (4) administered [24--4C]cholyltaurine and calculated its half-life as well as its rate of 7-dehydroxylation after bacterial deconjugation, but they gave no information on the taurine moiety. In this paper we