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在无机械负荷环境下,体内示踪剂在大鼠骨骼腔隙小管系统中的转运。

In vivo tracer transport through the lacunocanalicular system of rat bone in an environment devoid of mechanical loading.

作者信息

Knothe Tate M L, Niederer P, Knothe U

机构信息

Institute of Biomedical Engineering and Medical Informatics, University and Swiss Federal Institute of Technology, Zurich.

出版信息

Bone. 1998 Feb;22(2):107-17. doi: 10.1016/s8756-3282(97)00234-2.

Abstract

Although diffusion has been shown to be the major contributing mechanism for molecular transport in the extravascular spaces of organs and soft tissues, it is unlikely that diffusion alone can account for molecular transport in the porous, yet relatively impermeable matrix of bone. Rather, it has been proposed that fluid flow induced by the deformations that bone is subjected to during daily activities may promote molecular transport through convective mixing of fluids or enhancement of molecular transport from the capillaries to the outermost osteocytes within a given osteon. As the relative contribution of diffusive and convective transport in the bone matrix has not yet been elucidated, we conducted experiments to study the primary role of diffusion for molecular transport within bone and to establish a baseline for fluid transport whereby mechanical loading effects are negligible. Procion red and microperoxidase were utilized as short-term (i.e., low MW, transported on the order of minutes) and long-term (i.e., comparatively high MW, transported on the order of hours) molecular tracers, respectively, to elucidate in vivo the pathways and extent of transport in the metacarpus and tibia of 60-day-old (i.e., skeletally immature) and 180-day-old (i.e., skeletally mature) animals. The tracers were introduced intravenously and the animals were maintained in an anesthetized state for the duration of the experiment to prevent physiological loading. In short-term studies, procion red tracer distribution was highly dependent on bone structure, demarcating spaces apposing the vascular pathways in the trabecular bone of immature animals and vascular and extravascular pathways (i.e., specifically, the lacunocanalicular system) within compact bone of mature animals. In longer term studies using microperoxidase, reaction product was concentrated in soft tissues as well as along a subperiosteal and subendosteal band of bone. In contrast, little peroxidase reaction product was observed in the metacarpal and tibial cortices of either immature or mature animals. Based on the results of these studies, diffusive transport mechanisms may suffice to insure an adequate supply of small molecules, such as amino acids, to osteocytes in the midcortex within minutes. In contrast, diffusion alone may not be efficient for transport of larger molecules. Thus, another mechanism of transport, such as convective transport by means of load-induced fluid flow, may be necessary to provide a sufficient supply of larger molecules, such as proteins to osteocytes for the maintenance of metabolic activity, as well as for activation or suppression of modeling processes.

摘要

尽管扩散已被证明是器官和软组织血管外间隙中分子运输的主要作用机制,但仅靠扩散不太可能解释分子在多孔但相对不透水的骨基质中的运输。相反,有人提出,日常活动中骨骼所承受的变形引起的流体流动,可能通过流体的对流混合或增强分子从毛细血管到给定骨单位内最外层骨细胞的运输,来促进分子运输。由于扩散和对流运输在骨基质中的相对作用尚未阐明,我们进行了实验,以研究扩散在骨内分子运输中的主要作用,并建立一个流体运输的基线,在此基线中机械负荷效应可忽略不计。分别使用普施安红和微过氧化物酶作为短期(即低分子量,运输时间约为几分钟)和长期(即相对高分子量,运输时间约为几小时)分子示踪剂,以在体内阐明60日龄(即骨骼未成熟)和180日龄(即骨骼成熟)动物掌骨和胫骨中的运输途径和范围。示踪剂通过静脉注射引入,并且在实验期间动物保持麻醉状态以防止生理负荷。在短期研究中,普施安红示踪剂的分布高度依赖于骨结构,在未成熟动物小梁骨中划定与血管途径相邻的空间,在成熟动物密质骨中划定血管和血管外途径(即,具体来说,骨陷窝小管系统)。在使用微过氧化物酶的长期研究中,反应产物集中在软组织以及沿骨的骨膜下和骨内膜带。相比之下,在未成熟或成熟动物的掌骨和胫骨皮质中几乎未观察到过氧化物酶反应产物。基于这些研究结果,扩散运输机制可能足以确保在几分钟内为中皮质内的骨细胞提供足够的小分子供应,如氨基酸。相比之下,仅靠扩散对于较大分子的运输可能效率不高。因此,可能需要另一种运输机制,如通过负荷诱导的流体流动进行对流运输,以向骨细胞提供足够的较大分子供应,如蛋白质,以维持代谢活动,以及激活或抑制塑形过程。

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