用双能x线吸收法在体内评价表达肌肉生长抑制素原结构域的转基因小鼠的身体组成变化。

Growth Development and Aging Pub Date : 2007-01-01
A D Mitchell, R J Wall
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引用次数: 0

摘要

肌肉生长抑制素(MLC-pro)前域的过度表达会干扰肌肉生长抑制素的功能,从而促进肌肉生长。本研究的目的是利用双能x射线吸收仪(DXA)在体内监测10 ~ 91日龄对照组和转基因MLC-pro (TG)小鼠体成分的变化过程。通过G-3雄性TG小鼠与非TG雌性小鼠交配产生MLC-pro TG小鼠(n = 32)和同窝对照组小鼠(n = 28)。在第10天、第20天和此后的每周至第62天,最后在第91天对小鼠进行麻醉和DXA扫描。第34天,雄性TG小鼠体重明显高于对照组,且瘦质量(LM)较大,脂肪率(%F)较低(P < 0.05)。第91天,雄性TG小鼠体重增加15.6%,LM增加19.4%,%F减少22.4%,骨矿物质增加11.5%,骨密度增加4.4% (P < 0.05)。TG小鼠中较低的%F主要是由于LM的增加,而不是FM的减少。雌性小鼠TG与对照组无显著差异(P > 0.05)。兴趣区域分析被用来提供对后肢的单独测量。本研究通过DXA测定了MLC-pro TG与同窝对照小鼠体成分的发生和差异程度。
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In vivo evaluation of changes in body composition of transgenic mice expressing the myostatin pro domain using dual energy X-ray absorptiometry.

Over expression of the pro domain of myostatin (MLC-pro) interferes with myostatin function, thus promoting muscle growth. The purpose of this study was to use dual energy X-ray absorptiometry (DXA) to monitor, in vivo, the course of changes in body composition of control and MLC-pro transgenic (TG) mice between 10 and 91 days of age. MLC-pro TG (n = 32) and littermate control (n = 28) mice were produced by mating G-3 male TG mice with non-TG females. At days 10, 20 and weekly thereafter to day 62, and finally at day 91, the mice were anesthetized and scanned by DXA. By day 34, the body weight of the male TG mice was more than that of the control mice and was accompanied by a larger lean mass (LM) and a lower percentage of fat (%F) (P < 0.05). At day 91, the male TG mice had 15.6% greater body weight, 19.4% more LM, 22.4% lower %F, 11.5% more bone mineral, and 4.4% higher bone density (P < 0.05). The lower %F in the TG mice was due mainly to an increase in LM, rather than reduced FM. Measurements of the TG female mice were not different (P > 0.05) from those of control female mice. A region-of-interest analysis was used to provide a separate measure of the hind limb. By using DXA, this study determined the onset and degree of differences in body composition of MLC-pro TG and littermate control mice.

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