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“小个子”小鼠中的生长激素缺乏会导致身体成分异常、胰岛素样生长因子-I和胰岛素样生长因子结合蛋白-3(IGFBP-3)减少,但不影响IGFBP-2、-1或-4。

Growth hormone deficiency in 'little' mice results in aberrant body composition, reduced insulin-like growth factor-I and insulin-like growth factor-binding protein-3 (IGFBP-3), but does not affect IGFBP-2, -1 or -4.

作者信息

Donahue L R, Beamer W G

机构信息

Jackson Laboratory, Bar Harbor, Maine 04609.

出版信息

J Endocrinol. 1993 Jan;136(1):91-104. doi: 10.1677/joe.0.1360091.

Abstract

Although GH is known to regulate somatic growth during development, its role in regulating adult body composition is less well defined. The effects of GH on individual body compartments--water, fat, protein and mineral--are achieved both by the action of GH and by a GH-induced hormone, insulin-like growth factor-I (IGF-I). We used a genetic model of GH deficiency, the 'little' (gene symbol lit) mouse, to determine the GH regulation of IGF-I and its insulin-like growth factor-binding proteins (IGFBPs) and to define the interaction between these hormones and each body compartment in adults. Our results showed that GH-deficient lit/lit mice had reduced levels of serum IGF-I (range 38-130 micrograms/l) compared with normal lit/+ littermates (range 432-567 micrograms/l) between 2 and 52 weeks of age. The lit/lit mice did not experience the fivefold increase in IGF-I between 2 and 4 weeks of age that was seen in lit/+ mice. In lit/lit serum, overall binding of 125I-labelled IGF-I to the four IGFBPs was reduced, solely in response to a reduced amount of IGFBP-3. No overall differences were found between lit/lit and lit/+ mice in the binding of 125I-labelled IGF-I to IGFBP-2, -1 or -4. Age-related declines in IGF-I and IGFBPs were seen in lit/lit mice. However, adult levels of IGF-I were maintained in lit/+ mice to at least 52 weeks of age, as were levels of IGFBP-1 and -4, while IGFBP-3 and -2 declined with age. With respect to body composition, comparison of lit/lit with lit/+ mice showed that the lit/lit mice were characterized by abnormally large adipose tissue stores and reduced body water, protein and mineral from 2 weeks onward. These changes occurred despite normal energy intake in lit/lit mice up to 52 weeks of age, indicating that neither undernutrition nor hyperphagia is characteristic of this GH-induced model of obesity. Furthermore, lit/lit males accrued more body fat beginning at an earlier age than lit/lit females. With advancing age, the per cent body fat increased in both lit/lit and lit/+ mice, while the per cent body water and mineral declined. In lit/lit but not lit/+ mice, per cent protein also declined with age. The changes in body water and fat are attributable to lack of adequate GH in the genetically GH-deficient lit/lit mouse. On the other hand, the changes in body protein are more likely to be effects of IGF-I.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

尽管已知生长激素(GH)在发育过程中调节躯体生长,但其在调节成人体成分方面的作用尚不太明确。GH对个体身体成分(水、脂肪、蛋白质和矿物质)的影响是通过GH的作用以及一种由GH诱导的激素——胰岛素样生长因子-I(IGF-I)来实现的。我们利用一种生长激素缺乏的遗传模型——“小个子”(基因符号lit)小鼠,来确定GH对IGF-I及其胰岛素样生长因子结合蛋白(IGFBPs)的调节作用,并明确这些激素与成体中每个身体成分之间的相互作用。我们的结果显示,与正常的lit/+同窝小鼠(2至52周龄时范围为432 - 567微克/升)相比,生长激素缺乏的lit/lit小鼠血清IGF-I水平降低(范围为38 - 130微克/升)。lit/lit小鼠在2至4周龄时未经历lit/+小鼠中出现的IGF-I五倍增加。在lit/lit血清中,125I标记的IGF-I与四种IGFBPs的总体结合减少,这仅仅是由于IGFBP-3量的减少。在125I标记的IGF-I与IGFBPs -2、-1或 -4的结合方面,lit/lit和lit/+小鼠之间未发现总体差异。在lit/lit小鼠中观察到IGF-I和IGFBPs随年龄下降。然而,lit/+小鼠中IGF-I的成体水平至少维持到52周龄,IGFBP-1和 -4的水平也是如此,而IGFBP-3和 -2随年龄下降。关于身体成分,lit/lit与lit/+小鼠的比较表明,从2周龄起,lit/lit小鼠的特征是脂肪组织储存异常大,身体水分、蛋白质和矿物质减少。尽管lit/lit小鼠在52周龄前能量摄入正常,但仍发生了这些变化,这表明营养不良和食欲过盛都不是这种由GH诱导的肥胖模型的特征。此外,lit/lit雄性小鼠比lit/lit雌性小鼠更早开始积累更多身体脂肪。随着年龄增长,lit/lit和lit/+小鼠的体脂百分比均增加,而身体水分和矿物质百分比下降。在lit/lit小鼠而非lit/+小鼠中,蛋白质百分比也随年龄下降。身体水分和脂肪的变化归因于基因上生长激素缺乏的lit/lit小鼠中缺乏足够的GH。另一方面,身体蛋白质的变化更可能是IGF-I的作用。(摘要截断于400字)

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