Pioglitazone: effect on CYP3A4 activity
Autor: | Sandra N. Nowak, Anthony Clarke, David J. Edwards, Linda A. Jaber, Gail D. Anderson |
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Rok vydání: | 2002 |
Předmět: |
Adult
Male medicine.medical_specialty Hydrocortisone medicine.drug_class Urinary system Urine Pharmacokinetics Cytochrome P-450 Enzyme System Internal medicine medicine Cytochrome P-450 CYP3A Humans Hypoglycemic Agents Pharmacology (medical) Prospective Studies Thiazolidinedione Prospective cohort study Chromatography High Pressure Liquid Aged Pharmacology CYP3A4 Pioglitazone Chemistry Troglitazone Thiazoles Endocrinology Female Thiazolidinediones medicine.drug |
Zdroj: | Journal of clinical pharmacology. 42(12) |
ISSN: | 0091-2700 |
Popis: | Clinical studies demonstrate CYP3A4 enzyme induction with troglitazone, a thiazolidinedione derivative structurally related to pioglitazone. The objective of this prospective, open-label study conducted in healthy volunteers was to evaluate the influence of multiple-dose pioglitazone therapy on the urinary excretion ratio of 6-beta-hydroxycortisol to cortisol, an endogenous marker of CYP3A4 activity. Twelve subjects were given pioglitazone hydrochloride 45 mg daily for 14 days. Urine was collected over a 24-hour period before pioglitazone and after administration of the last tablet. Baseline and posttreatment CYP3A4 activity was assessed with the urinary 6-beta-hydroxycortisol/cortisol ratio. The mean +/- SD 6-beta-hydroxycortisol/cortisol ratios before and after treatment were 8.3 +/- 4.4 and 9.4 +/- 4.0, respectively (p = 0.29). The mean change from baseline was a nonsignificant 20.2%. Nine subjects had a small increase and 3 subjects had a reduction in the ratio. Using the ratio as a marker of CYP3A4 activity, the data support a lack of inductive effect on CYP3A4 by multiple-dose pioglitazone therapy. Thus, administration of pioglitazone should not result in clinically significant effects on the pharmacokinetics of other CYP3A4 substrates. |
Databáze: | OpenAIRE |
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