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给予三碘甲状腺原氨酸后大鼠肝脏细胞核三碘甲状腺原氨酸受体及线粒体α-磷酸甘油脱氢酶活性的序贯变化

Sequential changes in rat liver nuclear tri-iodothyronine receptors and mitochondrial alpha-glycerophosphate dehydrogenase activity after administration of tri-iodothyronine.

作者信息

Nakamura H, Hamada S, Imura H

出版信息

Biochem J. 1979 Aug 15;182(2):377-82. doi: 10.1042/bj1820377.

Abstract

The dynamics of the induction of nuclear tri-iodothyronine receptors and mitochondrial alpha-glycerophosphate dehydrogenase were studied in rat liver after a single injection of tri-iodothyronine. The maximal binding capacity (C(max.)) and association constant (K(a)) of the nuclear receptors were determined by Scatchard analyses with and without correction for the endogenous tri-iodothyronine measured by radioimmunoassay. The administration of tri-iodothyronine induced sequential increases in the concentration of nuclear receptors and alpha-glycerophosphate dehydrogenase activity in the liver. The nuclear-receptor concentration was increased to 2.5 times that in the hypothyroid rat 1 day after the administration of hormone, and then decreased, with a half-life of about 2 days. alpha-Glycerophosphate dehydrogenase activity changed in parallel with the nuclear-receptor concentration, showing a delayed response. The total amount of non-histone protein in the liver was significantly increased 3 days after the administration. It seems likely therefore that the tri-iodothyronine-induced increase in nuclear-receptor concentration is responsible, at least in part, for the induction of this enzyme. The possibility is also suggested that nuclear receptors may be one of the non-histone proteins selectively synthesized at an early stage of the hormonal stimulation. Throughout the time course, the K(a) values of the nuclear receptors for tri-iodothyronine remained unchanged, when corrected for endogenous tri-iodothyronine bound to the non-histone proteins, although they were apparently changed when the correction was not made. The results obtained provide further evidence for hormonal modulation of the nuclear receptors which is closely linked with the hormonal effect.

摘要

单次注射三碘甲状腺原氨酸后,对大鼠肝脏中核三碘甲状腺原氨酸受体和线粒体α-甘油磷酸脱氢酶的诱导动力学进行了研究。通过Scatchard分析测定核受体的最大结合容量(C(max.))和缔合常数(K(a)),分析时对通过放射免疫测定法测得的内源性三碘甲状腺原氨酸进行或不进行校正。三碘甲状腺原氨酸的给药导致肝脏中核受体浓度和α-甘油磷酸脱氢酶活性依次增加。给药后1天,核受体浓度增加至甲状腺功能减退大鼠的2.5倍,然后下降,半衰期约为2天。α-甘油磷酸脱氢酶活性与核受体浓度平行变化,显示出延迟反应。给药3天后,肝脏中非组蛋白的总量显著增加。因此,三碘甲状腺原氨酸诱导的核受体浓度增加似乎至少部分地导致了这种酶的诱导。还提出了一种可能性,即核受体可能是在激素刺激早期选择性合成的非组蛋白之一。在整个时间进程中,当对与非组蛋白结合的内源性三碘甲状腺原氨酸进行校正时,核受体对三碘甲状腺原氨酸的K(a)值保持不变,尽管在未进行校正时它们明显发生了变化。所获得的结果为与激素效应密切相关的核受体的激素调节提供了进一步的证据。

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