Inhibition of cytochrome P-450 2E1 by diallyl sulfide and its metabolites

• Published in: Chemical research in toxicology 1991-11, Vol.4 (6), p.642-647
• Main Authors: Brady, John F, Ishizaki, Hiroyuki, Fukuto, Jon M, Lin, Marie C, Fadel, Addi, Gapac, Jeanne M, Yang, Chung S
• Format: Article
• Language: English
• Subjects: Allyl Compounds - pharmacology; Animals; Biological and medical sciences; Carcinogenesis, carcinogens and anticarcinogens; Cytochrome P-450 CYP2E1; Cytochrome P-450 Enzyme Inhibitors; General aspects; Male; Medical sciences; Mixed Function Oxygenases - antagonists & inhibitors; Rats; Rats, Inbred Strains; Sulfides - metabolism; Sulfides - pharmacology; Sulfones - pharmacology; Sulfoxides - pharmacology; Tumors
• ISSN: 0893-228X; 1520-5010
• DOI: 10.1021/tx00024a008

Diallyl sulfide, a major flavor ingredient from garlic, was previously shown to inhibit chemically induced carcinogenesis and cytotoxicity in animal model systems. It modulated cytochrome P-450 compositions by inactivating P-450 2E1 and inducing P-450 2B1. The present studies examined the inhibition of P-450 2E1 mediated p-nitrophenol hydroxylase activity by diallyl sulfide and its putative metabolites diallyl sulfoxide and diallyl sulfone (DASO2). Each compound displayed competitive inhibition of p-nitrophenol hydroxylase activity in incubations using liver microsomes from acetone-pretreated male Sprague-Dawley rats. Preincubation of the microsomes with DASO2 inactivated p-nitrophenol hydroxylase activity in a process that was time- and NADPH-dependent and saturable, exhibited pseudo-first-order kinetics, was protected by alternate substrate, was accompanied by a loss of microsomal P-450-CO binding spectrum, and was unaffected by exogenous nucleophile. The Ki value for DASO2 was 188 microM and the maximal rate of inactivation was 0.32 min-1. DASO2 was ineffective in the inactivation of ethoxyresorufin dealkylase, pentoxyresorufin dealkylase, or benzphetamine demethylase activity. Purified P-450 2E1 in a reconstituted system was inactivated in a time- and NADPH-dependent manner by DASO2. The metabolic conversion of diallyl sulfide to the sulfoxide and sulfone was observed in vivo and in vitro. The results suggest that diallyl sulfide inhibits the metabolism of P-450 2E1 substrates by competitive inhibition mechanisms and by inactivating P-450 2E1 via a suicide-inhibitory action of DASO2.