首页> 外文期刊>Drug Metabolism and Disposition: The Biological Fate of Chemicals >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.
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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.

机译:小鼠血清中2,3,7,8-四氯二苯并-对-二恶英样多氯联苯同源物3,3',4,4',5-五氯联苯的甲状腺素水平降低的可能机制。

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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.
机译:用3,3',4,4',5-五氯联苯(CB126)(2.5 mg / kg ip)处理后2天,血清总甲状腺素(T(4))和游离T(4)水平显着降低, 3,7,8-四氯二苯并-对-二恶英(TCDD)敏感的C57BL / 6小鼠,但对TCDD耐药的DBA / 2小鼠不敏感。同时,肝T(4)-UDP-葡萄糖醛酸转移酶(T(4)-UGT)的水平和活性在C57BL / 6小鼠中显着增加,但在DBA / 2小鼠中则没有。此外,通过在C57BL / 6中进行CB126预处理,注射[(125)I] T(4)后胆汁中[[125] I] T(4)和[(125)I] T(4)葡萄糖醛酸的含量增加小鼠,但不是DBA / 2小鼠。在C57BL / 6小鼠中,通过CB126预处理也可促进从血清中清除[(125)I] T(4),而在DBA / 2小鼠中则没有。另一方面,通过CB126预处理未观察到[(125)I] T(4)的稳态分布体积和肝脏与血清的浓度比(K(p)值)的显着变化。任一种小鼠。因为在C57BL / 6小鼠中CB126预处理增加了肝脏重量,但在DBA / 2小鼠中却没有,因此仅在C57BL / 6小鼠中肝脏总[[125] I] T(4)增加。目前的发现表明,CB126介导的血清T(4)的降低是通过肝T(4)-UGT的增加和肝T(4)的积累以及肝肥大的发展而发生的。

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