Open AccessEffect of Erythromycin and Itraconazole on the Pharmacokinetics of Oral Lignocaine
Author(s) -
Isnhanni Mika H.,
Neuvonen Pertti J.,
Olkkola Klaus T.
Publication year - 1999
Publication title -
pharmacology & toxicology
Language(s) - English
Resource type - Journals
eISSN - 1600-0773
pISSN - 0901-9928
DOI - 10.1111/j.1600-0773.1999.tb00890.x
Subject(s) - itraconazole , pharmacokinetics , erythromycin , pharmacology , cyp3a4 , chemistry , bioavailability , oral administration , placebo , ketoconazole , crossover study , area under the curve , medicine , cytochrome p450 , metabolism , antibiotics , antifungal , biochemistry , alternative medicine , dermatology , pathology
Lignocaine is metabolized by cytochrome P450 3A4 enzyme (CYP3A4), and has a moderate to high extraction ratio resulting in oral bioavailability of 30%. We have studied the possible effect of two inhibitors of CYP3A4, erythromycin and itraconazole, on the pharmacokinetics of oral lignocaine in nine volunteers using a cross‐over study design. The subjects were given erythromycin orally (500 mg three times a day), itraconazole (200 mg once a day) or placebo for four days. On day 4, each subject ingested a single dose of 1 mg/kg of oral lignocaine. Plasma samples were collected until 10 hr and concentrations of lignocaine and its major metabolite, monoethylglycinexylidide were measured by gas chromatography. Both erythromycin and itraconazole increased the area under the lignocaine plasma concentration‐time curve [AUC(0–∞)] and lignocaine peak concentrations by 40–70% (P<0.05). Compared to placebo and itraconazole, erythromycin increased monoethylglycinexylidide peak concentrations by approximately 40% (P<0.01) and AUC(0–∞) by 60% (P<0.01). The clinical implication of this study is that erythromycin and itraconazole may significantly increase the plasma concentrations and toxicity of oral lignocaine. The extent of the interaction of lignocaine with these CYP3A4 inhibitors was, however, less than that of, e.g. midazolam or buspirone, and it did not correlate with the CYP3A4 inhibiting potency of erythromycin and itraconazole.