TY - JOUR
T1 - Significance of renal γ-butyrobetaine hydroxylase for carnitine biosynthesis in man
AU - Rebouche, C. J.
AU - Engel, A. G.
N1 - Copyright:
Copyright 2004 Elsevier B.V., All rights reserved.
PY - 1980
Y1 - 1980
N2 - Carnitine biosynthesis was studied in man and rat. Three healthy adult men were given intravenous injections of 1 mCi of [methyl-3H]ε-N-trimethyl-L-lysine, a precursor of carnitine. Labeled metabolites of this compound were monitored in serum and urine at 2, 6, 12, 24, and 48 h. At least nine radioactive metabolites were detected. For each collection period, the specific activity of urinary carnitine exceeded the average serum specific activity. In man the amount of labeled carnitine in urine was 2 to 8 times greater than labeled γ-butyrobetaine (the immediate precursor of carnitine). In similar experiments in rats (intravenous injection of 0.1 mCi of [methyl-3H]ε-N-trimethyl-L-lysine the specific activity of carnitine in urine was always lower than the corresponding average specific activity in serum. Between 0 and 2 h after administration of labeled precursor , the animals excreted large amounts of labeled γ-butyrobetaine but with labeled carnitine. Significant γ-butyrobetaine, 2-oxoglutarate dioxygenase (EC 1.14.11.1) activity was found in human kidney but this activity was absent in rat kidney. The results indicate that in man and rat the kidney accumulates intravenously administered [methyl-3H]ε-N-trimethyl-L-lysine This compound is metabolized predominantly to γ-butyrobetaine in rat kidney and to carnitine in human kidney. In both species, the synthesized products are at least partially leaked (either by secretion or by passive diffusion down a concentration gradient) into the renal tubular lumen from which they are either reabsorbed into the circulation for distribution to other tissues or excreted.
AB - Carnitine biosynthesis was studied in man and rat. Three healthy adult men were given intravenous injections of 1 mCi of [methyl-3H]ε-N-trimethyl-L-lysine, a precursor of carnitine. Labeled metabolites of this compound were monitored in serum and urine at 2, 6, 12, 24, and 48 h. At least nine radioactive metabolites were detected. For each collection period, the specific activity of urinary carnitine exceeded the average serum specific activity. In man the amount of labeled carnitine in urine was 2 to 8 times greater than labeled γ-butyrobetaine (the immediate precursor of carnitine). In similar experiments in rats (intravenous injection of 0.1 mCi of [methyl-3H]ε-N-trimethyl-L-lysine the specific activity of carnitine in urine was always lower than the corresponding average specific activity in serum. Between 0 and 2 h after administration of labeled precursor , the animals excreted large amounts of labeled γ-butyrobetaine but with labeled carnitine. Significant γ-butyrobetaine, 2-oxoglutarate dioxygenase (EC 1.14.11.1) activity was found in human kidney but this activity was absent in rat kidney. The results indicate that in man and rat the kidney accumulates intravenously administered [methyl-3H]ε-N-trimethyl-L-lysine This compound is metabolized predominantly to γ-butyrobetaine in rat kidney and to carnitine in human kidney. In both species, the synthesized products are at least partially leaked (either by secretion or by passive diffusion down a concentration gradient) into the renal tubular lumen from which they are either reabsorbed into the circulation for distribution to other tissues or excreted.
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M3 - Article
C2 - 6773946
AN - SCOPUS:0019129839
SN - 0021-9258
VL - 255
SP - 8700
EP - 8705
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 18
ER -