RT Journal Article
SR Electronic
T1 RELATIONSHIPS AMONG PLASMA [2-<sup>13</sup>C]URACIL CONCENTRATIONS, BREATH <sup>13</sup>CO<sub>2</sub> EXPIRATION, AND DIHYDROPYRIMIDINE DEHYDROGENASE (DPD) ACTIVITY IN THE LIVER IN NORMAL AND DPD-DEFICIENT DOGS
JF Drug Metabolism and Disposition
JO Drug Metab Dispos
FD American Society for Pharmacology and Experimental Therapeutics
SP 381
OP 387
DO 10.1124/dmd.104.001032
VO 33
IS 3
A1 Makoto Inada
A1 Yukihiro Hirao
A1 Toshihisa Koga
A1 Minoru Itose
A1 Jun-ichi Kunizaki
A1 Takefumi Shimizu
A1 Hitoshi Sato
YR 2005
UL http://dmd.aspetjournals.org/content/33/3/381.abstract
AB Dihydropyrimidine dehydrogenase (DPD), the first enzyme in the sequential metabolism of pyrimidine, regulates blood concentrations of 5-fluorouracil and is deeply involved in its toxicity. This study was designed to examine the effects of a DPD inhibitor on blood concentrations of [2-13C]uracil ([13C]uracil) and 13CO2 concentration (Δ13C) expired in breath after oral or intravenous administration of [13C]uracil to DPD-suppressed dogs prepared by pretreatment with 5-(trans-2-bromovinyl)uracil (BVU), a DPD inhibitor. Area under the curve (AUCt) of [13 C]uracil after oral administration at 20 μmol/kg to dogs pretreated with BVU at 2, 5, and 40 μmol/kg were 37-, 88- and 120-fold higher than those of the control dogs, respectively. In contrast, breath AUCt values of Δ13C were reduced to 0.88-, 0.47- and 0.13-fold the control values, respectively. Upon intravenous administration of [13C]uracil at 20 μmol/kg to dogs pretreated with BVU at 0.5, 2, and 40 μmol/kg, blood AUCt values of [13C]uracil were 1.4-, 4.2-, and 13-fold higher than those of the control group, respectively, whereas breath AUCt values were reduced to 1.0-, 0.83-, and 0.07-fold the respective control values. DPD activities in the liver cytosol of dogs pretreated with BVU at 0.5, 2, 5, and 40 μmol/kg were decreased to 0.71-, 0.12-, 0.06-, and 0.04-fold those of the control dogs, respectively. These findings demonstrate that breath output (Δ13C) is a good marker of hepatic DPD activity in vivo. The American Society for Pharmacology and Experimental Therapeutics