TY - JOUR T1 - GALACTOSAMINE PREVENTS ETHINYLESTRADIOL-INDUCED CHOLESTASIS JF - Drug Metabolism and Disposition JO - Drug Metab Dispos SP - 993 LP - 997 DO - 10.1124/dmd.106.009308 VL - 34 IS - 6 AU - Fernando A. Crocenzi AU - José M. Pellegrino AU - Viviana A. Catania AU - Marcelo G. Luquita AU - Marcelo G. Roma AU - Aldo D. Mottino AU - Enrique J. Sánchez Pozzi Y1 - 2006/06/01 UR - http://dmd.aspetjournals.org/content/34/6/993.abstract N2 - Ethinylestradiol (EE) induces intrahepatic cholestasis in experimental animals being its derivative, ethinylestradiol 17β-glucuronide, a presumed mediator of this effect. To test whether glucuronidation is a relevant step in the pathogenesis of cholestasis induced by EE (5 mg/kg b.wt. s.c. for 5 consecutive days), the effect of simultaneous administration of galactosamine (200 mg/kg b.wt. i.p.) on biliary secretory function was studied. A single injection of this same dose of galactosamine was able to decrease hepatic UDP-glucuronic acid (UDP-GA) levels by 85% and excretion of EE-17β-glucuronide after administration of a tracer dose of [3H]EE by 40%. Uridine (0.9 g/kg b.wt. i.p.) coadministration reverted the effect of galactosamine on hepatic UDP-GA levels and restored the excretion of [3H]EE-17β-glucuronide. When administered for 5 days, galactosamine itself did not alter any of the serum markers of liver injury studied (aspartate aminotransferase, alanine aminotransferase, and alkaline phosphatase) or biliary secretory function. When coadministered with EE, galactosamine partially prevented the impairment induced by this estrogen in total bile flow, the bile-salt-independent fraction of bile flow, basal bile salt secretion, and the secretory rate maximum of tauroursodeoxycholate. Uridine coadministration partially prevented galactosamine from exerting its anticholestatic effects. In conclusion, galactosamine administration partially prevented EE-induced cholestasis by a mechanism involving decreased UDP-GA availability for subsequent formation of EE 17β-glucuronide. The evidence thus supports the hypothesis that EE 17β-glucuronide is involved in the pathogenesis of EE cholestasis. The American Society for Pharmacology and Experimental Therapeutics ER -