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. 1999 Mar;47(3):299-305.
doi: 10.1046/j.1365-2125.1999.00890.x.

Cytochrome P450 isoform selectivity in human hepatic theobromine metabolism

S Gates  1 , J O Miners
Affiliations

Cytochrome P450 isoform selectivity in human hepatic theobromine metabolism

S Gates et al. Br J Clin Pharmacol. 1999 Mar.

Abstract

Aims: The plasma clearance of theobromine (TB; 3,7-dimethylxanthine) is known to be induced in cigarette smokers. To determine whether TB may serve as a model substrate for cytochrome P450 (CYP) 1A2, or possibly other isoforms, studies were undertaken to identify the individual human liver microsomal CYP isoforms responsible for the conversion of TB to its primary metabolites.

Methods: The kinetics of formation of the primary TB metabolites 3-methylxanthine (3-MX), 7-methylxanthine (7-MX) and 3,7-dimethyluric acid (3,7-DMU) by human liver microsomes were characterized using a specific hplc procedure. Effects of CYP isoform-selective xenobiotic inhibitor/substrate probes on each pathway were determined and confirmatory studies with recombinant enzymes were performed to define the contribution of individual isoforms to 3-MX, 7-MX and 3,7-DMU formation.

Results: The CYP1A2 inhibitor furafylline variably inhibited (0-65%) 7-MX formation, but had no effect on other pathways. Diethyldithiocarbamate and 4-nitrophenol, probes for CYP2E1, inhibited the formation of 3-MX, 7-MX and 3,7-DMU by approximately 55-60%, 35-55% and 85%, respectively. Consistent with the microsomal studies, recombinant CYP1A2 and CYP2E1 exhibited similar apparent Km values for 7-MX formation and CYP2E1 was further shown to have the capacity to convert TB to both 3-MX and 3,7-DMU.

Conclusions: Given the contribution of multiple isoforms to 3-MX and 7-MX formation and the negligible formation of 3,7-DMU in vivo, TB is of little value as a CYP isoform-selective substrate in humans.

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Figures

Figure 1
Figure 1
Pathways of theobromine metabolism in humans.
Figure 2
Figure 2
Representative Eadie-Hofstee plots for the conversion of TB to 3-methylxanthine and, 7-methylxanthine (panel a), and 3,7-dimethyluric acid (panel b) by human liver microsomes (liver #1). Points are experimentally derived values while the solid lines in panel a show the model-generated curves of best fit.
Figure 3
Figure 3
Eadie-Hofstee plots for the conversion of TB to 7-MX by recombinant CYP1A2 (panel a) and CYP2E1 (panel b). Points are experimentally derived values while the solid lines show the model-generated curves of best fit.
See this image and copyright information in PMC

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