Prolonged unloading in growing rats reduces cortical osteocyte lacunar density and volume in the distal tibia.

Autor: Britz HM; University of Saskatchewan, Saskatoon, Canada., Carter Y, Jokihaara J, Leppänen OV, Järvinen TL, Belev G, Cooper DM
Jazyk: angličtina
Zdroj: Bone [Bone] 2012 Nov; Vol. 51 (5), pp. 913-9. Date of Electronic Publication: 2012 Aug 16.
DOI: 10.1016/j.bone.2012.08.112
Abstrakt: Bone dynamically adapts its structure to the environmental demands placed upon it. Load-related stimuli play an important role in this adaptation. It has been postulated that osteocytes sense changes in these stimuli and initiate adaptive responses, across a number of scales, through a process known as mechanotransduction. While much research has focused on gross and tissue-level adaptation, relatively little is known regarding the relation between cellular-level features (e.g. osteocyte lacunar density, volume and shape) and loading. The increasing availability of high resolution 3D imaging modalities, including synchrotron-based techniques, has made studying 3D cellular-level features feasible on a scale not previously possible. The primary objective of this study was to test the hypothesis that unloading (sciatic neurectomy) during growth results in altered osteocyte lacunar density in the tibial diaphysis of the rat. Secondarily, we explored a potential effect of unloading on mean lacunar volume. Lacunar density was significantly (p<0.05) lower in immobilized bones (49,642 ± 11,955 lacunae per mm(3); n=6) than in control bones (63,138 ± 1956 lacunae per mm(3); n=6). Mean lacunar volume for immobilized bones (209 ± 72 μm(3); n=6) was significantly smaller (p<0.05) than that for the control bones (284 ± 28 μm(3); n=6). Our results demonstrate that extreme differences in loading conditions, such as those created by paralysis, do indeed result in changes in osteocyte lacunar density and volume. Further investigation is warranted to examine relations between these measures and more subtle variation in loading as well as pathological states, which have been linked to alterations in mechanotransduction.
(Copyright © 2012 Elsevier Inc. All rights reserved.)
Databáze: MEDLINE
Externí odkaz: