Armbrecht Harvey J, Lakshmi Vijaya M, Wickstra Jason, Hsu Fong Fu, Zenser Terry V
Geriatric Center (11G-JB), St. Louis VA Medical Center, St. Louis, MO 63125, USA.
Drug Metab Dispos. 2007 Apr;35(4):633-9. doi: 10.1124/dmd.106.013532. Epub 2007 Jan 24.
The incidence of colon cancer increases with age, and this may be related to altered metabolism and disposition of carcinogens. One such carcinogen implicated in colon cancer is the heterocyclic amine found in well done meat, 2-amino-3-methylimidazo[4,5-f]quinoline (IQ). The purpose of these studies was to determine whether the disposition and metabolism of IQ changes with age, comparing young (3-month) and old (22- to 24-month) male F344 rats. Animals were treated with vehicle or beta-naphthoflavone (BNF), an inducer of drug-metabolizing cytochromes P450. Disposition and metabolism of IQ were determined after i.p. injection of radiolabeled IQ. Urinary IQ metabolites were identified and quantitated by high-performance liquid chromatography and mass spectroscopy. In BNF-treated animals, total radiolabeled IQ excretion by old rats was less than half that of young rats. Binding of radiolabeled IQ metabolites by the old kidney was 10 times higher than that of the young. There were no age differences in intestinal and hepatic binding. There was a significant age-related increase in IQ conjugation to glucuronic acid and a decrease in conjugation to sulfate regardless of treatment. The induction of renal CYP1A1, a major P450 involved in IQ metabolism, by BNF did not change with age. Changes in IQ metabolism with age along with altered renal function may contribute to the decreased urinary excretion and increased renal binding of IQ and/or its metabolites seen in the old animals.
结肠癌的发病率随年龄增长而增加,这可能与致癌物的代谢和处置改变有关。一种与结肠癌有关的致癌物是在熟透的肉类中发现的杂环胺,即2-氨基-3-甲基咪唑[4,5-f]喹啉(IQ)。这些研究的目的是比较年轻(3个月)和年老(22至24个月)的雄性F344大鼠,以确定IQ的处置和代谢是否随年龄变化。动物接受载体或β-萘黄酮(BNF,一种药物代谢细胞色素P450的诱导剂)处理。腹腔注射放射性标记的IQ后,测定IQ的处置和代谢情况。通过高效液相色谱和质谱法鉴定并定量尿液中的IQ代谢物。在接受BNF处理的动物中,老年大鼠放射性标记IQ的总排泄量不到年轻大鼠的一半。老年大鼠肾脏对放射性标记IQ代谢物的结合能力比年轻大鼠高10倍。肠道和肝脏的结合能力没有年龄差异。无论是否接受处理,与葡萄糖醛酸的IQ结合随年龄显著增加,与硫酸盐的结合减少。BNF对参与IQ代谢的主要细胞色素P450 CYP1A1的诱导作用不随年龄变化。IQ代谢随年龄的变化以及肾功能的改变可能导致老年动物尿液排泄减少以及IQ和/或其代谢物在肾脏中的结合增加。