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生长中大鼠的后肢卸载:一种预测太空飞行期间骨骼变化的模型。

Hindlimb unloading of growing rats: a model for predicting skeletal changes during space flight.

作者信息

Morey-Holton E R, Globus R K

机构信息

Life Sciences Division, NASA-Ames Research Center, Moffett Field, CA 94035-1000, USA.

出版信息

Bone. 1998 May;22(5 Suppl):83S-88S. doi: 10.1016/s8756-3282(98)00019-2.

Abstract

A model that uses hindlimb unloading of rats was developed to study the consequences of skeletal unloading and reloading as occurs during and following space flight. Studies using the model were initiated two decades ago and further developed at National Aeronautics and Space Administration (NASA)-Ames Research Center. The model mimics some aspects of exposure to microgravity by removing weightbearing loads from the hindquarters and producing a cephalic fluid shift. Unlike space flight, the forelimbs remain loaded in the model, providing a useful internal control to distinguish between the local and systemic effects of hindlimb unloading. Rats that are hindlimb unloaded by tail traction gain weight at the same rate as pairfed controls, and glucocorticoid levels are not different from controls, suggesting that systemic stress is minimal. Unloaded bones display reductions in cancellous osteoblast number, cancellous mineral apposition rate, trabecular bone volume, cortical periosteal mineralization rate, total bone mass, calcium content, and maturation of bone mineral relative to controls. Subsequent studies reveal that these changes also occur in rats exposed to space flight. In hindlimb unloaded rats, bone formation rates and masses of unloaded bones decline relative to controls, while loaded bones do not change despite a transient reduction in serum 1,25-dihydroxyvitamin D (1,25D) concentrations. Studies using the model to evaluate potential countermeasures show that 1,25D, growth hormone, dietary calcium, alendronate, and muscle stimulation modify, but do not completely correct, the suppression of bone growth caused by unloading, whereas continuous infusion of transforming growth factor-beta2 or insulin-like growth factor-1 appears to protect against some of the bone changes caused by unloading. These results emphasize the importance of local as opposed to systemic factors in the skeletal response to unloading, and reveal the pivotal role that osteoblasts play in the response to gravitational loading. The hindlimb unloading model provides a unique opportunity to evaluate in detail the physiological and cellular mechanisms of the skeletal response to weightbearing loads, and has proven to be an effective model for space flight.

摘要

为了研究太空飞行期间及之后发生的骨骼卸载和重新加载的后果,开发了一种使用大鼠后肢卸载的模型。使用该模型的研究始于二十年前,并在美国国家航空航天局(NASA)艾姆斯研究中心进一步发展。该模型通过去除后肢的负重负荷并产生头向体液转移来模拟暴露于微重力的某些方面。与太空飞行不同,模型中的前肢仍承受负荷,这为区分后肢卸载的局部和全身效应提供了有用的内部对照。通过尾部牵引进行后肢卸载的大鼠体重增加速度与配对喂养的对照组相同,糖皮质激素水平与对照组无差异,这表明全身应激最小。与对照组相比,卸载的骨骼显示松质骨成骨细胞数量减少、松质骨矿物质沉积率降低、小梁骨体积减小、皮质骨膜矿化率降低、总骨量减少、钙含量降低以及骨矿物质成熟度降低。随后的研究表明,这些变化也发生在暴露于太空飞行的大鼠身上。在后肢卸载的大鼠中,相对于对照组,卸载骨骼的骨形成率和骨量下降,而尽管血清1,25 - 二羟基维生素D(1,25D)浓度暂时降低,但承受负荷的骨骼并未改变。使用该模型评估潜在对策的研究表明,1,25D、生长激素、膳食钙、阿仑膦酸盐和肌肉刺激可改变但不能完全纠正卸载引起的骨生长抑制,而持续输注转化生长因子 - β2或胰岛素样生长因子 - 1似乎可防止卸载引起的一些骨骼变化。这些结果强调了局部因素而非全身因素在骨骼对卸载反应中的重要性,并揭示了成骨细胞在对重力负荷反应中所起的关键作用。后肢卸载模型为详细评估骨骼对负重负荷反应的生理和细胞机制提供了独特的机会,并且已被证明是一种有效的太空飞行模型。

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