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大鼠肝脏中UDP-葡萄糖醛酸基转移酶对甲状腺激素的活性:各种酶诱导剂处理后对血清甲状腺激素水平的诱导作用及影响

Hepatic UDP-glucuronyltransferase(s) activity toward thyroid hormones in rats: induction and effects on serum thyroid hormone levels following treatment with various enzyme inducers.

作者信息

Saito K, Kaneko H, Sato K, Yoshitake A, Yamada H

机构信息

Environmental Health Science Laboratory, Sumitomo Chemical Co., Ltd., Osaka, Japan.

出版信息

Toxicol Appl Pharmacol. 1991 Oct;111(1):99-106. doi: 10.1016/0041-008x(91)90138-5.

Abstract

Induction of hepatic UDP-glucuronyltransferase(s) (hUDP-GT(s] activity toward thyroid hormones and the relationship between the activity and the serum thyroid hormones or the thyroid stimulating hormone (TSH) level were examined in male Sprague-Dawley rats after four consecutive ip doses of various hepatic enzyme inducers at 75-150 mg/kg/day. hUDP-GT activity toward thyroxine (T4; hUDP-GT-T4) was induced by treatment with beta-naphthoflavone, 3-methylcholanthrene (3-MC), polychlorinated biphenyls, or pregnenolone-16 alpha-carbonitrile. However, no significant induction was observed for isosafrole administration and in the cases of phenobarbital and 1,1,1-trichloro-2,2-bis(p-chlorophenyl)ethane slight decreases were found. The induction profile of hUDP-GT-T4 for these inducers was approximately the same as that of hUDP-GT activity toward triiodothyronine (T3; hUDP-GT-T3), indicating that these two thyroid hormones (T4 and T3) are glucuronidated by the same hUDP-GT(s). Moreover, the induction profile of both hUDP-GT-T4 and hUDP-GT-T3 was similar to that of hUDP-GT toward 1-naphthol, but not chloramphenicol, suggesting that T4 and T3 belong to the so-called group-1 substrates which are preferentially glucuronidated by hUDP-GT(s) inducible by treatment with 3-MC. Decreases in serum T4 levels clearly correlated with an increase in hUDP-GT-T4 activity, indicating that serum T4 levels are directly affected by hUDP-GT-T4 activity. However, no direct correlation between decrease in thyroid hormone levels and compensatory increase in TSH levels was found.

摘要

在雄性Sprague-Dawley大鼠中,连续4天腹腔注射剂量为75 - 150 mg/kg/天的各种肝酶诱导剂后,检测肝UDP-葡萄糖醛酸基转移酶(hUDP-GT)对甲状腺激素的诱导作用以及该酶活性与血清甲状腺激素或促甲状腺激素(TSH)水平之间的关系。用β-萘黄酮、3-甲基胆蒽(3-MC)、多氯联苯或孕烯醇酮-16α-腈处理可诱导hUDP-葡萄糖醛酸基转移酶对甲状腺素(T4;hUDP-GT-T4)的活性。然而,给予异黄樟素未观察到明显的诱导作用,而给予苯巴比妥和1,1,1-三氯-2,2-双(对氯苯基)乙烷时,hUDP-GT-T4活性略有下降。这些诱导剂对hUDP-GT-T4的诱导模式与hUDP-葡萄糖醛酸基转移酶对三碘甲状腺原氨酸(T3;hUDP-GT-T3)的活性诱导模式大致相同,表明这两种甲状腺激素(T4和T3)由相同的hUDP-GT进行葡萄糖醛酸化。此外,hUDP-GT-T4和hUDP-GT-T3的诱导模式与hUDP-葡萄糖醛酸基转移酶对1-萘酚而非氯霉素的诱导模式相似,这表明T4和T3属于所谓的1组底物,它们优先被3-MC诱导的hUDP-GT进行葡萄糖醛酸化。血清T4水平的降低与hUDP-GT-T4活性的增加明显相关,表明血清T4水平直接受hUDP-GT-T4活性的影响。然而,未发现甲状腺激素水平降低与TSH水平的代偿性升高之间存在直接相关性。

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