Yamamoto T, Pierce W M, Hurst H E, Chen D, Waddell W J
Department of Pharmacology and Toxicology, University of Louisville School of Medicine, KY 40292.
Drug Metab Dispos. 1988 May-Jun;16(3):355-8.
Ethanol has been shown to inhibit the localization of [ethyl-1-14C] urethane in the male mouse, but the effect of ethanol on the metabolism of urethane has not been clarified. Consequently, the concentration of unchanged urethane was determined in the blood of male mice up to 11 hr after oral administration of urethane with or without ethanol. A high and constant blood level of urethane persisted for 8 hr after the administration of an ethanolic solution of [ethyl-1-14C] urethane (125 mumol/kg, 10 muCi/20 g of mouse, 5 g of ethanol per kg, po); the blood level of ethanol was at or above 150 mg/dl during these 8 hr. In contrast, rapid clearance of radioactivity was observed in mice treated with [ethyl-1-14C]urethane dissolved in water. Coadministration of ethanol with urethane decreased the rate of 14CO2 expiration; furthermore, covalent binding with liver protein was delayed about 8 hr and was less than that in the group treated with urethane in water. The metabolism of urethane and production of 14CO2 from [carbonyl-14C]urethane by mouse liver homogenate in vitro were inhibited by the presence of ethanol (greater than 10 mM); these concentrations of ethanol in vitro are about the same as those that are inhibitory in vivo, but the extent of inhibition suggests that the liver is not the only site of metabolism of urethane. These results indicate that ethanol can inhibit the initial metabolism of urethane, prevent the formation of active metabolites, and allow urethane to persist in blood.
乙醇已被证明可抑制雄性小鼠体内[乙基-1-¹⁴C]氨基甲酸乙酯的定位,但乙醇对氨基甲酸乙酯代谢的影响尚未明确。因此,在雄性小鼠口服氨基甲酸乙酯(无论是否同时给予乙醇)后长达11小时的血液中,测定了未变化的氨基甲酸乙酯的浓度。给予[乙基-1-¹⁴C]氨基甲酸乙酯乙醇溶液(125 μmol/kg,每20克小鼠10 μCi,每千克含5克乙醇,经口给药)后,氨基甲酸乙酯在血液中维持了8小时的高且稳定的水平;在这8小时内,乙醇的血液水平处于或高于150 mg/dl。相比之下,在给予溶于水的[乙基-1-¹⁴C]氨基甲酸乙酯的小鼠中,观察到放射性快速清除。乙醇与氨基甲酸乙酯共同给药降低了¹⁴CO₂呼出率;此外,与肝蛋白的共价结合延迟了约8小时,且低于给予溶于水的氨基甲酸乙酯的组。体外实验中,乙醇(大于10 mM)的存在抑制了小鼠肝脏匀浆对氨基甲酸乙酯的代谢以及[羰基-¹⁴C]氨基甲酸乙酯产生¹⁴CO₂的过程;体外这些乙醇浓度与体内具有抑制作用的浓度大致相同,但抑制程度表明肝脏并非氨基甲酸乙酯代谢的唯一部位。这些结果表明,乙醇可抑制氨基甲酸乙酯的初始代谢,防止活性代谢产物的形成,并使氨基甲酸乙酯在血液中持续存在。