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多氯联苯(氯丹-500)对大鼠和小鼠血清甲状腺激素水平的影响。

Effects of polychlorinated biphenyls, kanechlor-500, on serum thyroid hormone levels in rats and mice.

作者信息

Kato Yoshihisa, Haraguchi Koichi, Yamazaki Tomoaki, Ito Yuriko, Miyajima Shoji, Nemoto Kiyomitsu, Koga Nobuyuki, Kimura Ryohei, Degawa Masakuni

机构信息

School of Pharmaceutical Sciences, University of Shizuoka, 52-1, Yada, Shizuoka 422-8526, Japan.

出版信息

Toxicol Sci. 2003 Apr;72(2):235-41. doi: 10.1093/toxsci/kfg025.

Abstract

Effects of a commercial polychlorinated biphenyls mixture, Kanechlor-500 (KC500), on the levels of serum thyroid hormones such as total thyroxine (T4) and triiodothyronine (T3) were examined comparatively in male Wistar rats and ddy mice. Serum T4 levels were significantly decreased in both rats and mice 4 days after a single ip injection of KC500 (100 mg/kg body weight), whereas decreased levels of T3 were observed in mice but not in rats. In addition, no significant change in the level of serum thyroid stimulating hormone was observed in either rats or mice. Hepatic UDP-glucuronosyltransferases (UDP-GTs) UGT1A1 and UGT1A6, which efficiently mediate glucuronidation of T4 and promote the excretion of the hormones, were induced by KC500 in rats but not in mice. Hepatic microsomal cytochrome P450 (P450) content and the microsomal activity for 7-ethoxy-, 7-pentoxy-, and 7-benzoyloxy-resorufin dealkylations were significantly increased by KC500 in both rats and mice, although the magnitude of increase in the enzyme activities was higher in rats than in mice. The difference in the increase in the activity of microsomal enzymes, including UDP-GT and P450, between KC500-treated rats and mice was not correlated with that in the level of hepatic methylsulfonyl-PCB metabolites. In the present study, we found for the first time that the decrease in serum T4 levels by KC-500 in mice occurred without increase in hepatic UDP-GTs, UGT1A1 and UGT1A6, responsible for T4 glucuronidation. The present findings further suggested that although the decrease in serum T4 levels in KC500-treated rats would occur at least in part through the induction of the UDP-GTs, it might not be dependent on only the increase in the enzymes.

摘要

在雄性Wistar大鼠和ddy小鼠中,比较研究了市售多氯联苯混合物氯丹-500(KC500)对血清甲状腺激素水平(如总甲状腺素(T4)和三碘甲状腺原氨酸(T3))的影响。单次腹腔注射KC500(100mg/kg体重)4天后,大鼠和小鼠的血清T4水平均显著降低,而小鼠的T3水平降低,大鼠则未出现这种情况。此外,大鼠和小鼠的血清促甲状腺激素水平均未观察到显著变化。肝脏尿苷二磷酸葡萄糖醛酸转移酶(UDP-GTs)UGT1A1和UGT1A6可有效介导T4的葡萄糖醛酸化并促进激素排泄,KC500可诱导大鼠的这两种酶,但对小鼠无此作用。KC500可使大鼠和小鼠肝脏微粒体细胞色素P450(P450)含量以及微粒体对7-乙氧基、7-戊氧基和7-苯甲酰氧基试卤灵脱烷基的活性显著增加,尽管大鼠酶活性的增加幅度高于小鼠。KC500处理的大鼠和小鼠之间,包括UDP-GT和P450在内的微粒体酶活性增加的差异与肝脏甲基磺酰基多氯联苯代谢物水平的差异无关。在本研究中,我们首次发现,KC-500使小鼠血清T4水平降低,而负责T4葡萄糖醛酸化的肝脏UDP-GTs、UGT1A1和UGT1A6并未增加。本研究结果进一步表明,虽然KC500处理的大鼠血清T4水平降低至少部分是通过诱导UDP-GTs实现的,但可能不仅仅取决于这些酶的增加。

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