Prolonging disuse in aged mice amplifies cortical but not trabecular bones' response to mechanical loading
File(s)J257_DeSouza_JMNI_2017_as_accepted.pdf (3.44 MB)
Accepted version
Author(s)
Type
Journal Article
Abstract
Objective:
Short-term neurectomy-induced disuse (SN) has been shown to restore load responses in aged mice. We examined whether this restoration was further enhanced in both cortical and trabecular bone by simply extending the SN.
Methods:
Following load: strain calibration, tibiae in female C57BL/J6 mice at 8, 14 and 20 weeks and 18 months (n=8/group) were loaded and bone changes measured. Effects of long-term SN examined in twenty-six 18 months-old mice, neurectomised for 5 or 100 days with/without subsequent loading. Cortical and trabecular responses were measured histomorphometrically or by micro-computed tomography.
Results:
Loading increased new cortical bone formation, elevating cross-sectional area in 8, 14 and 20 week-old (p <0.05), but not 18 month-old aged mice. Histomorphometry showed that short-term SN reinstated load-responses in aged mice, with significant 33% and 117% increases in bone accrual at 47% and 37%, but not 27% of tibia length. Cortical responses to loading was heightened and widespread, now evident at all locations, following prolonged SN (108, 167 and 98% at 47, 37 and 27% of tibial length, respectively). In contrast, loading failed to modify trabecular bone mass or architecture.
Conclusions:
Mechanoadaptation become deficient with ageing and prolonging disuse amplifies this response in cortical but not trabecular bone.
Short-term neurectomy-induced disuse (SN) has been shown to restore load responses in aged mice. We examined whether this restoration was further enhanced in both cortical and trabecular bone by simply extending the SN.
Methods:
Following load: strain calibration, tibiae in female C57BL/J6 mice at 8, 14 and 20 weeks and 18 months (n=8/group) were loaded and bone changes measured. Effects of long-term SN examined in twenty-six 18 months-old mice, neurectomised for 5 or 100 days with/without subsequent loading. Cortical and trabecular responses were measured histomorphometrically or by micro-computed tomography.
Results:
Loading increased new cortical bone formation, elevating cross-sectional area in 8, 14 and 20 week-old (p <0.05), but not 18 month-old aged mice. Histomorphometry showed that short-term SN reinstated load-responses in aged mice, with significant 33% and 117% increases in bone accrual at 47% and 37%, but not 27% of tibia length. Cortical responses to loading was heightened and widespread, now evident at all locations, following prolonged SN (108, 167 and 98% at 47, 37 and 27% of tibial length, respectively). In contrast, loading failed to modify trabecular bone mass or architecture.
Conclusions:
Mechanoadaptation become deficient with ageing and prolonging disuse amplifies this response in cortical but not trabecular bone.
Date Issued
2017-09-01
Date Acceptance
2017-06-26
Citation
JOURNAL OF MUSCULOSKELETAL & NEURONAL INTERACTIONS, 2017, 17 (3), pp.218-225
ISSN
1108-7161
Publisher
JMNI
Start Page
218
End Page
225
Journal / Book Title
JOURNAL OF MUSCULOSKELETAL & NEURONAL INTERACTIONS
Volume
17
Issue
3
Copyright Statement
© Journal of Musculoskeletal and Neuronal Interactions. This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported (https://creativecommons.org/licenses/by-nc-sa/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Identifier
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000410545600011&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=1ba7043ffcc86c417c072aa74d649202
Subjects
Science & Technology
Life Sciences & Biomedicine
Neurosciences
Physiology
Neurosciences & Neurology
Mechanical Loading
Osteoporosis
Sciatic Neurectomy
Bone
Ageing
ADAPTIVE RESPONSE
RESORPTION
C57BL/6
1109 Neurosciences
1116 Medical Physiology
Endocrinology & Metabolism
Publication Status
Published