黄酮类化合物诱导大鼠肝脏药物代谢酶活性的时间过程。

M. Siess, Mastropaolo Jp, M. Canivenc-Lavier, M. Suschetet
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引用次数: 40

摘要

研究了连续饲喂黄酮类化合物(黄酮、黄酮和橘皮素)对大鼠肝脏药物代谢酶的影响,以确定饲喂多长时间才能达到最大诱导,并确定是否能长期维持最大诱导。在第一个实验中,大鼠接受含有10 mmol类黄酮/kg干物质的日粮,持续4、8、16和32 d。第二个实验旨在观察前4 d诱导的时间过程。诱导动力学取决于类黄酮的化学结构,并且不同酶的诱导动力学不同。黄酮增加P450 1A和P450 2B载脂蛋白,刺激多种酶活性。P450 1A1/2蛋白、乙氧基间苯二酚o -去乙基化酶(EROD)和甲氧基间苯二酚o -去甲基化酶(MROD)活性早在第一次给药后6 h就出现了显著升高,并在饲喂第4 d逐渐升高。P450 2B1/2蛋白与P450 1A1/2蛋白相比,P450 2B1/2蛋白和戊氧基间苯二酚o -去烯基化酶(PROD)活性也有所增加,但有滞后期。第4 d, EROD和MROD活性下降,第32 d, PROD活性保持稳定。谷胱甘肽转移酶(GST)和对硝基苯酚udp -葡萄糖醛酸转移酶(UGT)活性也有所提高。UGT在饲喂第4 d达到最大诱导,GST在饲喂较长时间(16 d)后达到最大诱导。黄酮处理主要诱导P450 2B1/2蛋白和PROD、GST和UGT活性。饲喂4 d后,P450 2B1/2蛋白和PROD活性下降,而GST和UGT活性保持稳定。橘皮素治疗产生的变化与黄酮相似,但幅度较小,延迟时间较长。
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Time course of induction of rat hepatic drug-metabolizing enzyme activities following dietary administration of flavonoids.
Effects of continuous feeding flavonoids (flavone, flavanone, and tangeretin) on drug-metabolizing enzymes in rat liver were investigated to ascertain how long feeding is required to reach maximal induction and to determine whether maximal induction is maintained for a long period of feeding. In the first experiment rats received a diet containing 10 mmol flavonoid/kg dry matter for 4, 8, 16, or 32 d. The second experiment was designed to examine the time course for induction during the first 4 d. The kinetics of induction depended on the chemical structure of the flavonoid and was different from one enzyme to another. Flavone increased P450 1A and P450 2B apoproteins and stimulated many enzyme activities. A significant increase of P450 1A1/2 proteins, ethoxyresorufin O-deethylase (EROD), and methoxyresorufin O-demethylase (MROD) activities occurred as early as 6 h after the first administration, and a gradual increase was observed up to 4 d of feeding. P450 2B1/2 proteins and pentoxyresorufin O-depentylase (PROD) activity were also increased but after a lag period when compared with P450 1A1/2 proteins. EROD and MROD activities declined after 4 d, whereas PROD activity remained steady during 32 d of flavone feeding. Glutathione transferase (GST) and p-nitrophenol UDP-glucuronosyl transferase (UGT) activities were also increased. The maximal induction was reached by 4 d of feeding for UGT and after a longer duration of feeding (16 d) for GST. Flavanone treatment induced mostly P450 2B1/2 proteins and PROD, GST, and UGT activites. After 4 d of feeding, P450 2B1/2 proteins and PROD activity declined whereas GST and UGT activities remained steady. Tangeretin treatment produced changes similar to flavone but of lesser magnitude and after a longer delay.
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