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一种可能的机制,解释 2,3,7,8-四氯二苯并对二恶英样多氯联苯同系物 3,3',4,4',5-五氯联苯在小鼠体内导致血清甲状腺素水平降低的原因。

A possible mechanism for the decrease in serum thyroxine level by a 2,3,7,8-tetrachlorodibenzo-p-dioxin-like polychlorinated biphenyl congener, 3,3',4,4',5-pentachlorobiphenyl in mice.

机构信息

Kagawa School of Pharmaceutical Sciences, Tokushima Bunri University, Sanuki, Kagawa, Japan.

出版信息

Drug Metab Dispos. 2010 Jan;38(1):150-6. doi: 10.1124/dmd.109.029348.

Abstract

Serum total thyroxine (T(4)) and free T(4) levels were markedly decreased 7 days after treatment with 3,3',4,4',5-pentachlorobiphenyl (CB126) (2.5 mg/kg i.p.) in 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD)-sensitive C57BL/6 mice but not in TCDD-resistant DBA/2 mice. At the same time, the level and activity of hepatic T(4)-UDP-glucuronosyltransferase (T(4)-UGT) were significantly increased in C57BL/6 mice but not in DBA/2 mice. Furthermore, the amounts of biliary [(125)I]T(4) and [(125)I]T(4) glucuronide after injection of [(125)I]T(4) were increased by CB126 pretreatment in C57BL/6 mice but not in DBA/2 mice. Clearance of [(125)I]T(4) from serum was also promoted by CB126 pretreatment in C57BL/6 mice but not in DBA/2 mice. On the other hand, no significant changes in the steady-state volumes of distribution of [(125)I]T(4) and in the concentration ratio (K(p) value) of the liver to serum by CB126 pretreatment were observed in either strain of mice. Because liver weight was increased by CB126 pretreatment in C57BL/6 mice but not in DBA/2 mice, hepatic total [(125)I]T(4) was increased only in C57BL/6 mice. The present findings indicate that CB126-mediated decrease in serum T(4) occurs through the increase in hepatic T(4)-UGT and the enhanced accumulation of hepatic T(4) along with development of liver hypertrophy.

摘要

血清总甲状腺素(T(4))和游离 T(4)水平在 3,3',4,4',5-五氯联苯(CB126)(2.5 mg/kg,ip)治疗后 7 天明显降低在对 2,3,7,8-四氯二苯并对二恶英(TCDD)敏感的 C57BL/6 小鼠中,但在 TCDD 抗性 DBA/2 小鼠中则不然。同时,肝 T(4)-UDP-葡糖醛酸基转移酶(T(4)-UGT)的水平和活性在 C57BL/6 小鼠中显著增加,但在 DBA/2 小鼠中则不然。此外,在 C57BL/6 小鼠中,注射[(125)I]T(4)后胆汁中[(125)I]T(4)和[(125)I]T(4)葡萄糖醛酸的量增加,但在 DBA/2 小鼠中则不然。CB126 预处理也促进了 C57BL/6 小鼠血清中[(125)I]T(4)的清除,但在 DBA/2 小鼠中则不然。另一方面,在两种品系的小鼠中,CB126 预处理对[(125)I]T(4)的稳态分布容积和肝/血清浓度比(K(p)值)没有显著影响。因为 CB126 预处理增加了 C57BL/6 小鼠的肝重,但没有增加 DBA/2 小鼠的肝重,所以只有 C57BL/6 小鼠的肝总[(125)I]T(4)增加。本研究结果表明,CB126 介导的血清 T(4)降低是通过增加肝 T(4)-UGT 和增强肝 T(4)的积累以及肝肥大的发展而发生的。

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