Inhibition of Cytochrome P450 2C9 Expression and Activity In Vitro by Allyl Isothiocyanate

Abstract

The growing interest in the use of natural herbal products and dietary supplements to treat and prevent diseases raises the question of medicinal drug safety. Allyl isothiocyanate, a hydrolysis product of a glucosinolate, sinigrin, has multiple beneficial properties, and based on this fact, allyl isothiocyanate-containing dietary supplements have been developed. To date, no studies of the effects of this compound on the cytochrome P450 2C9 have been reported. In this study, we found that allyl isothiocyanate reduced catalytic activity, messenger ribonucleic acid, and protein expression of cytochrome P450 2C9 in HepaRG cells. An investigation of the transcriptional activity of the pregnane X receptor and the constitutive androstane receptor revealed that allyl isothiocyanate disrupted the transcriptional coregulation effects of the pregnane X receptor/constitutive androstane receptor with several important coregulators and interfered with the assembly of transcriptional complexes of the cytochrome P450 2C9 pregnane X receptor/constitutive androstane receptor-response element. The decrease of cytochrome P450 2C9 expression and activity mediated by allyl isothiocyanate suggested that this agent could alter the metabolism of drugs metabolized by cytochrome P450 2C9. This may cause food/dietary supplement-drug interactions or alter the therapeutic effects, and even the toxicity of drugs coadministered with allyl isothiocyanate. Since the consumption of allyl isothiocyanate-containing food/dietary supplements continues to increase, it is important to predict and ultimately avoid interactions with concomitant drugs. It is required that these possible pharmacokinetic interactions be characterized and the recommendations available to patients and healthcare professionals be improved.

In vitro inhibitory effects of cepharanthine on human liver cytochrome P450 enzymes

“…As previous studies reported, CYP2E1 and CYP2C9 play a vital role in the metabolism of many drugs (He et al 2009;Lim et al 2014;Xu et al 2017;Bedada and Neerati 2018). There are also many drugs inhibiting the activity of CYP2E1 and CYP2C9 (Pan et al 2010;Jiang et al 2016;Liu et al 2017;Hao et al 2018), and we get similar results in the study of CEP.…”

In vitro Inhibitory Effects of Cynaroside on Human Liver Cytochrome P450 Enzymes

“…CYP2C9 is also playing an important role in the metabolism of many drugs [25]. Our study showed that cynaroside competitively inhibited human liver microsomal CYP2C9 activity.…”

“…However, the results also indicated that cynaroside is a timedependent inhibitor for CYP3A4 with K inact /K I value of 0.049/11.62 μmol/L -1 min -1 , which revealed that cynaroside would inhibit the activity of CYP3A4 with increase of preincubation time of concentration. Therefore, in order to avoid adverse drug interactions, cynaroside should not be used with other drugs metabolized by CYP3A4, such as amiodarone, acetaminophen, cyclosporin A, lansoprazole, felodipine, meloxicam, and ketoconazole [25].…”

In vitro inhibitory effects of kaempferitrin on human liver cytochrome P450 enzymes

“…CYP2C9 also plays an important role in the metabolism of many drugs (Lim et al. 2014). Our study showed that KF competitively inhibited human liver microsomal CYP2C9 activity.…”