In vitro inhibition of dihydropyridine oxidation and aflatoxin B1 activation in human liver microsomes by naringenin and other flavonoids

Abstract

Recent in vivo studies in humans have shown a dramatic effect of grapefruit juice in blocking the oxidation of dihydropyridine calcium channel blockers. The flavonold naringin is the most abundant natural product specific for grapefruit and related citrus-the aglycone naringenin, known to be readily formed from naringin in humans, was found to inhibit the oxidation of the dlhydropyridines nifedipine and felodipine in human liver microsomal preparations. These observations were of interest in light of the knowledge that the same human liver cytochrome P450 (IIIA4) appears to be a major catalyst in both nifedipine oxidation and aflatoxin B₁ activation. Several flavones inhibited the in vitro activation of alfatoxin B₁ in a system employing umuC gene activation due to DNA damage in Salmonlla typhimurium TA1535/pSK1OO2, with naringenin being as effective as any. The high concentration of derivatives of naringenin in certain citrus fruits may be of relevance to cancer chemoprevention involving those carcinogens that are activated by cytochrome P-450IIIA4.