Effect of ethanol on spectral binding, inhibition, and activity of CYP3A4 with an antiretroviral drug nelfinavir

• Published in: Biochemical and biophysical research communications 2010-11, Vol.402 (1), p.163-167
• Main Authors: Kumar, Santosh, Earla, Ravinder, Jin, Mengyao, Mitra, Ashim K., Kumar, Anil
• Format: Article
• Language: English
• Subjects: Alcohol; Alcoholism; Alcoholism - complications; Alcoholism - enzymology; Anti-Retroviral Agents - pharmacokinetics; Anti-Retroviral Agents - pharmacology; Binding Sites - drug effects; CYP3A4; Cytochrome P-450 CYP3A - chemistry; Cytochrome P-450 CYP3A - metabolism; Cytochrome P-450 CYP3A Inhibitors; Ethanol - metabolism; Ethanol - pharmacology; HIV Infections - complications; HIV Infections - drug therapy; HIV Infections - enzymology; Human immunodeficiency virus; Humans; Inactivation, Metabolic; Inhibition; Liver - enzymology; Metabolism; Nelfinavir; Nelfinavir - pharmacokinetics; Nelfinavir - pharmacology; Protein Binding - drug effects; Spectral binding
• ISSN: 0006-291X; 1090-2104
• DOI: 10.1016/j.bbrc.2010.10.014

► Methanol, ethanol, isopropanol, isobutanol, and isoamyl alcohol exhibit type I spectra with CYP3A4, and ethanol shows the highest binding affinity for CYP3A4. ► Ethanol increases the spectral binding affinity of nelfinavir to CYP3A4. ► Ethanol increases the inhibition of CYP3A4 by nelfinavir. ► Ethanol decreases the catalytic efficiency of nelfinavir metabolism. Cytochrome P450 3A4 (CYP3A4) is the most abundant CYP enzyme in the liver and metabolizes approximately 50% of the drugs, including antiretrovirals. Although CYP3A4 induction by ethanol and impact of CYP3A4 on drug metabolism and toxicity is known, CYP3A4-ethanol physical interaction and its impact on drug binding, inhibition, or metabolism is not known. Therefore, we studied the effect of ethanol on binding and inhibition of CYP3A4 with a representative protease inhibitor, nelfinavir, followed by the effect of alcohol on nelfinavir metabolism. Our initial results showed that methanol, ethanol, isopropanol, isobutanol, and isoamyl alcohol bind in the active site of CYP3A4 and exhibit type I spectra. Among these alcohol compounds, ethanol showed the lowest K D (5.9 ± 0.34 mM), suggesting its strong binding affinity with CYP3A4. Ethanol (20 mM) decreased the K D of nelfinavir by >5-fold (0.041 ± 0.007 vs. 0.227 ± 0.038 μM). Similarly, 20 mM ethanol decreased the IC 50 of nelfinavir by >3-fold (2.6 ± 0.5 vs. 8.3 ± 3.1 μM). These results suggest that ethanol facilitates binding of nelfinavir with CYP3A4. Furthermore, we performed nelfinavir metabolism using LCMS. Although ethanol did not alter k cat, it decreased the K m of nelfinavir, suggesting a decrease in catalytic efficiency ( k cat/ K m). This is an important finding because alcoholism is prevalent in HIV-1-infected persons and alcohol is shown to decrease the response to antiretroviral therapy.