首页> 美国卫生研究院文献>The Journal of Clinical Investigation >Decreased serum triiodothyronine in starving rats is due primarily to diminished thyroidal secretion of thyroxine.
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Decreased serum triiodothyronine in starving rats is due primarily to diminished thyroidal secretion of thyroxine.

机译:饥饿的大鼠血清三碘甲状腺素减少主要是由于甲状腺素甲状腺分泌减少所致。

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摘要

Although thyroxine (T4) 5'-deiodinase activity is diminished in liver homogenates of starved rats, no information is available regarding the effect of starvation on net T4 to triiodothyronine (T3) conversion in the intact rat. It appeared important to clarify this relationship since rat liver homogenates are widely used as a model for the study of the factors responsible for reduced circulating T3 in chronically ill and calorically deprived patients. In contrast to the expected selective decrease in circulating T3 levels in calorically restricted humans due to diminished T4 to T3 conversion, 5 d of starvation of two groups of male Sprague-Dawley rats resulted, paradoxically, in a greater decrease in serum T4 than in serum T3 levels. Kinetic studies show that starvation is associated with no change in the metabolic clearance rate (MCR) of T3, a 20% increase in the MCR of T4, a 67% reduction in turnover rate of T4, but only a 58% reduction in the turnover rate of T3. Moreover, in the first group of rats studied, direct chromatographic analysis of the isotopic composition of total body homogenates after the injection of 125I-T4 showed that 21.8% of T4 is converted to T3 in control rats and 28.8% in starved rats, suggesting that virtually all extrathyroidal T3 in starved and control rats is derived from the peripheral conversion of T4, and that there is little or no direct thyroidal secretion of T3. Our findings strongly point to a reduced thyroidal secretion of T4 as the primary cause of the observed reduction in circulating T3. Since the mechanisms leading to reduced levels of plasma T3 differ in humans and rats, it may be important to reexamine the use of liver homogenate preparations as models for study of the pathogenesis of the "low T3 syndrome" in humans.
机译:尽管在饥饿的大鼠的肝匀浆中甲状腺素(T4)5'-脱碘酶的活性降低,但是在完整大鼠中,饥饿对净T4转化为三碘甲状腺素(T3)的影响尚无相关信息。阐明这种关系似乎很重要,因为大鼠肝匀浆被广泛用作研究慢性病和热量缺乏患者中循环T3降低的因素的模型。与由于T4到T3转化减少导致热量受限的人体内循环T3水平的选择性降低相反,两组雄性Sprague-Dawley大鼠饥饿5 d矛盾的是,血清T4的降低大于血清中的T4的降低。 T3级。动力学研究表明,饥饿与T3的代谢清除率(MCR)不变,T4的MCR增加20%,T4的周转率降低67%,但周转率仅降低58%有关T3的比率。此外,在研究的第一组大鼠中,注射125I-T4后对全身匀浆的同位素组成进行直接色谱分析,结果表明,在对照组中,有21.8%的T4转化为T3;在饥饿的大鼠中有28.8%的T4转化为T3。实际上,饥饿和对照大鼠中的所有甲状腺外T3都源自T4的外周转化,并且很少或没有T3的直接甲状腺分泌。我们的发现强烈指出,T4甲状腺分泌减少是观察到的循环T3减少的主要原因。由于导致人类和大鼠血浆T3水平降低的机制不同,因此重新检查肝匀浆制剂作为研究人类“低T3综合征”发病机理的模型可能很重要。

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