Karageorgou M, Vasiliou V, Nebert D W, Marselos M
Department of Pharmacology, University of Ioannina Medical School, Greece.
Biochem Pharmacol. 1995 Dec 22;50(12):2113-7. doi: 10.1016/0006-2952(95)02085-3.
Using six ligands that bind to four different receptors in the nuclear steroid/thyroid hormone superfamily, we have examined the effects of these chemicals on induction of the cytosolic aldehyde dehydrogenase (ALDH3c) activity by 3-methylcholanthrene (3MC) in rat liver and uterus. In contrast to negligible activities in the untreated rat, ALDH3c enzyme activities are induced after a single dose of 3MC. Hepatic ALDH3c induction is decreased 60% to 90% when 3MC is administered together with any of the following ligands: estradiol, testosterone, progesterone, hydrocortisol, diethylstilbestrol, or tamoxifen. None of these same doses of chemicals, administered alone, affects ALDH3c enzyme activity. In addition, when these ligands are injected 2 days after 3MC, no changes are observed in liver or uterus ALDH3c induction. These results suggest that ligands that bind to different receptors in the nuclear steroid/thyroid hormone superfamily might inhibit the ALD3H3c induction process by polycyclic aromatic hydrocarbons; the molecular mechanism(s) of this inhibitory effect is not yet understood.
我们使用了六种与核甾体/甲状腺激素超家族中的四种不同受体结合的配体,研究了这些化学物质对3-甲基胆蒽(3MC)诱导大鼠肝脏和子宫中胞质醛脱氢酶(ALDH3c)活性的影响。与未处理大鼠中可忽略不计的活性相反,单次给予3MC后可诱导ALDH3c酶活性。当3MC与以下任何一种配体一起给药时,肝脏中ALDH3c的诱导降低60%至90%:雌二醇、睾酮、孕酮、氢化可的松、己烯雌酚或他莫昔芬。这些相同剂量的化学物质单独给药时,均不影响ALDH3c酶活性。此外,当这些配体在3MC注射2天后注射时,肝脏或子宫中ALDH3c的诱导未观察到变化。这些结果表明,与核甾体/甲状腺激素超家族中不同受体结合的配体可能会抑制多环芳烃对ALD3H3c的诱导过程;这种抑制作用的分子机制尚不清楚。