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. 2018 Jan 9;8:173. doi: 10.1038/s41598-017-18037-y

Occlusal disharmony-induced stress causes osteopenia of the lumbar vertebrae and long bones in mice

Yasuhiro Shimizu 1, Masud Khan 2,3,4, Genki Kato 4, Kazuhiro Aoki 2,✉, Takashi Ono 1
PMCID: PMC5760568  PMID: 29317698

Abstract

Excessive exposure to glucocorticoids causes osteoporosis in children and adults. Occlusal disharmony is known to induce an increase in serum corticosteroid levels in murine models, but the influence of occlusal disharmony-induced stress on the bone mass during the growth period has not yet been clarified. The purpose of this study was to investigate whether occlusal disharmony-induced stress decreases bone mass. Five-week-old C57BL/6J male mice were used. A 0.5-mm increase in the vertical height of occlusion was used to induce occlusal disharmony for a period of 7 days. Serum corticosterone levels were significantly higher on post-induction day 7, with radiological evidence of osteopenia of the third lumbar vertebra and long bones of the hind limbs. Osteopenia was associated with a reduction of the mechanical properties of the tibia and femur, with significant suppression of bone formation parameters and an increase in bone resorption parameters, as evaluated by bone histomorphometric analysis of the tibial/femur metaphysis. Our findings at the level of bones were supported by our assessment of serum markers of systemic metabolism. Therefore, occlusal disharmony-induced stress may lead to osteopenia and reduce the mechanical strength of bone through an increase in serum glucocorticoid levels in mice.

Introduction

Occlusal disharmony frequently occurs during growth due to mixed dentition, as the primary dentition is changing to permanent dentition. Several lines of evidence indicate that occlusal disharmony increases serum corticosteroid levels in young animals. As the serum corticosteroid level is considered to be a marker of ‘stress’ in rodents, it is plausible that occlusal disharmony would cause stress1–4. The high frequency of bruxism (teeth grinding) during the period of growth further suggests the possible existence of occlusal disharmony-induced stress in childhood5–7. By contrast, it is well known that excessive exposure to glucocorticoids causes osteopenia8. As an example, the use of steroid medications in children for the treatment of immune-related diseases, such as asthma and skin allergies, commonly results in bone-related side effects, including fractures and slowed bone growth9. Given the significant effects of stress-induced hormone on bone metabolism10, evaluation of the effect of occlusal disharmony-induced stress on skeletal tissue is warranted.

Our aim in this study was to use a mouse model of occlusal disharmony to evaluate the effects of occlusal disharmony-induced stress on bone mass and bone mineral density, as well as on the mechanical properties of the long bones and lumbar vertebrae, which are expected to be differentially affected by mechanical loading11–13.

Results

Increase in serum corticosterone level with occlusal disharmony

Serum corticosterone levels were measured at baseline and after the induction of occlusal disharmony (Fig. 1). Serum corticosterone levels were significantly higher in the disharmony than in the control group on post-induction days 1, 3 and 7 (Fig. 2, Supplementary Fig. S1).

Figure 1.

Figure 1

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The occlusal disharmony model, showing (a) the experimental protocol and (b) the occlusal height adjustment, using a composite resin to increase the occlusal height. The height of the lower incisors was adjusted by 0.5 mm in the vertical direction. Ctr, control group; Dis, occlusal disharmony group.

Figure 2.

Figure 2

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Measurements of serum corticosterone levels (a) on day 1 after induction of occlusal disharmony, and (b) on post-induction day 7. Values are expressed as the mean ± SD; Ctr, control group; Dis, occlusal disharmony group; *p < 0.05 versus the control group (Ctr).

Osteopenia associated with occlusal disharmony

Micro-computed tomography (CT) analysis provided evidence of osteopenia of the third lumbar vertebra in the disharmony group, which was associated with a significant decrease in structural parameters (bone volume and trabecular thickness), as well as an increase in trabecular bone pattern factor (TBPf, 1/mm), which is indicative of a disconnected trabecular structure (Fig. 3). The association between occlusal disharmony and osteopenia was confirmed at the femoral neck, an area known to be influenced by excessive exposure to glucocorticoids8.

Figure 3.

Figure 3

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Representative three-dimensional micro-CT images of the structural changes of the trabecular bone of the third lumbar vertebra is shown (a); the bars represent 600 μm and 200 μm in low and high magnified images, respectively. The bone structural parameters are shown in (b): the percentage of bone volume per tissue volume (BV/TV, %), trabecular thickness (Tb.Th, μm), trabecular number (Tb.N, 1/mm), and trabecular bone pattern factor (TBPf, 1/mm). Values are expressed as the mean ± SD; Ctr, control group; Dis, occlusal disharmony group; *p < 0.05 versus the control group (Ctr).

Decrease in bone mineral density and the mechanical parameters of long bones with occlusal disharmony

Effects of occlusal disharmony on the mechanical properties of long bones, and specifically on cortical and trabecular bone, were evaluated by pQCT analysis. Total bone mineral density, the trabecular index of bone mineral density and cortex-related indices, namely cortical bone area and cortical thickness, were significantly suppressed in the tibial metaphysis of mice in the disharmony group, compared to those in the control group (Fig. 4a–e). The mechanical strength indices (SSI and torsion index) of the tibial metaphysis were also significantly lower in the disharmony group than in the control group (Fig. 4f,g). Similarly, the total bone mineral density, the trabecular related index, the cortex-related indices, and the mechanical strength parameters were also significantly lower in the distal femur of mice in the disharmony group than those in the control group. Lower total bone mineral density and cortex-related indices were also observed in the region of the femur (Supplementary Fig. S2).

Figure 4.

Figure 4

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A representative pQCT image of the proximal tibia for quantitative analyses (bar, 1 mm) is shown in (a). The colour calibration for bone mineral density is shown in the right bar. The reduction in maximum bone mineral density with occlusal disharmony is indicated. Other measured variables of bone structure are shown as follows: total mineral density of the proximal tibia (b); total mineral density of tibia (c); cortical bone area of the proximal tibia (d); cortical thickness of the proximal tibia (e); trabecular density of the proximal tibia (f); strength strain index (SSI) of the proximal tibia (g); and torsion index of the proximal tibia. Values are expressed as the mean ± SD; Ctr, control group; Dis, occlusal disharmony group; *p < 0.05; **p < 0.01 versus the control group (Ctr).

Decreased bone formation parameters in the secondary spongiosa of the tibial metaphysis with occlusal disharmony

Calcein injections were administered on the day of induction and on post-induction day 6 to evaluate effects of occlusal disharmony on bone formation activity. Evaluation of un-decalcified thin sections under fluorescent microscopy revealed a decrease in the distance between the calcein double labels in disharmony group, compared to the control group (Fig. 5a). A bone histomorphometric study was performed to confirm these histological observations. The mineral apposition rate (MAR), which is indicative of the bone formation capacity of osteoblasts, was significantly decreased in the disharmony group, compared to the control group (Fig. 5b), along with a smaller mineralizing surface per bone surface (MS/BS; Fig. 5c). Consequently, changes in the bone formation rate (BFR), which reflects the total amount of bone formation in a day, were in the same direction as those in MAR and MS/BS (BFR is calculated as MS/BS × MAR), being significantly lower in the occlusal disharmony than in the control group (Fig. 5d). Serum osteocalcin levels were measured to clarify effects of occlusal disharmony on systemic bone formation activity, with significant decreases in serum levels identified on post-induction day 1 (Fig. 5e).

Figure 5.

Figure 5

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Bone formation parameters, with calcein injections administered at the time of induction of occlusal disharmony (day 0) and on post-induction (day 6). Measured parameters were as follows: (a) magnified images of calcein double labelling of trabecular bone (bar, 10 μm); (b) mineral apposition rate (MAR); (c) mineralizing surface per bone surface (MS/BS); (d) bone formation rate (BFR); (e) serum osteocalcin level on day 1; and (f) serum osteocalcin level on day 7. Values are expressed as the mean ± SD; Ctr, control group; Dis, occlusal disharmony group; *p < 0.05 versus the control group (Ctr); ****p < 0.0001 versus the control group (Ctr).

The osteoclast surface (Oc.S/BS) and the number of osteoclasts (N.Oc/BV) were comparable between the disharmony and control groups (Fig. 6a,b). Serum TRACP 5b level, which is indicative of bone resorption activity, was not modified on post-induction day 1, but did decrease significantly in the disharmony group on post-induction day 7 (Fig. 6c and d). Urine CTX levels were comparable between the disharmony and control groups on day 0 and on post-induction day 1 (Fig. 7a and b).

Figure 6.

Figure 6

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Bone resorption parameters showing: (a) the osteoclast surface (Oc.S/BS); (b) the number of osteoclasts (N.Oc/BV); (c) serum TRACP 5b level on day 1.; and (d) serum TRACP 5b level on day 7. Values are expressed as the mean ± SD; Ctr, control group; Dis, occlusal disharmony group; *p < 0.05 versus the control group (Ctr).

Figure 7.

Figure 7

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(a) Urine CTX levels of the control (Ctr) group on days 0 and 1. (b) Urine CTX levels of group Dis on days 0 and 1. Values are expressed as the mean ± SD; Ctr, control group; Dis, occlusal disharmony group.

High-turnover bone remodelling in the middle of the observation period in the occlusal disharmony group

Histopathological examination of the cortical bone of the femur showed an increase in bone formation in the experimental group on day 7 (Supplementary Figs S3 and S4a). Moreover, the serum level of TRACP 5b, obtained in the middle of the period of observation, was indicative of a significant increase in bone resorption activity in the disharmony group on post-induction day 5 (Supplementary Fig. S4b). These results are suggestive of a high turnover rate of bone remodelling in the middle of the observation period.

Increased osteocyte apoptosis in the cortical bone area in the occlusal disharmony group

Histological examination of the cortical bone area of the femur, using nuclear staining with DNA-specific fluorescent Hoechst 33258 on post-induction day 3, revealed an increase in chromatin condensation in osteocytes in the occlusal disharmony group (Supplementary Fig. S4b).

Discussion

Our aim was to evaluate potential effects of occlusal disharmony during growth, using an animal model that has previously been used in research. Our research was motivated by the knowledge of the negative impact of high serum glucocorticoid levels, as well as inadequate nutrition and low physical activity, on the development of peak bone mass in early life8,9,14–17. We provide evidence of an increase in serum corticosterone levels with occlusal disharmony, with secondary effects on the bone, which are consistent with previously reported findings1–4. Faecal corticosterone levels were not influenced by the modification in diet, namely from pellet to powder, in either the disharmony or the control group. Moreover, as all other experimental conditions, except the use of the composite resin, were comparable between the disharmony and control groups, the measured increase in serum corticosterone levels can only be explained by the induction of occlusal disharmony. The increase in serum levels of corticosterone in the disharmony group exceeded the 200 ng/ml threshold considered to reflect ‘stress’ in rodents (Fig. 2)3,18.

Following the induction of occlusal disharmony, body weight decreased for several days, with animals subsequently recovering to a level where there was no significant difference in body weight between animals in the disharmony and control group, as has been previously reported. Certainly, the acute decrease in food consumption following induction of occlusal disharmony might have influenced the bone loss in the experimental group. Previous studies, using an OVX model, have reported an initial increase in bone resorption markers immediately following a decrease in calcium intake, which was followed by an increase in the level of bone formation markers19. However, we did not identify this trend in our model, with no increase in either bone formation or resorption markers on post-induction day 1, indicating that the increase in glucocorticoid levels was the main cause of bone loss.

Serum levels of corticosterone were increased after induction of occlusal disharmony, with a 2.4-fold increase in the disharmony group compared with the control group on post-induction day 1, a 2.3-fold increase on post-induction day 3 and a 1.5-fold increase on post-induction day 7 (Fig. 2, Supplementary Fig. S1). It is possible that serum levels of corticosterone would continue to decrease over time in the disharmony group, as animals adapt to the stress of occlusal disharmony. However, we have confirmed the induction of significantly higher serum corticosterone levels in our model during the experimental period, with the corticosteroid level in the experimental group significantly decreasing on day 7, compared to initial stage (day 1 and 3) of occlusal disharmony, this difference confirmed by multiple intergroup comparisons using Fisher’s protected least significant difference (PLSD) as a post hoc test (Supplementary Fig. S5). We also observed that the increase in bone resorption marker identified on day 5 in the occlusal disharmony group was no longer evident on day 7, a result which might be comparable to using a GR antagonist treatment (Supplementary Fig. S8). Further research is warranted, including the use of GR antagonist treatment, to clarify the causal effect of increased serum corticosteroid levels on bone in the occlusal disharmony group.

Previous studies have reported that, following an initial adaptation to stress, occlusal disharmony increases the response of the hypothalamic–pituitary–adrenal (HPA) axis to subsequent new stress. Therefore, eliminating stress induced by malocclusion during the period of growth could be important to optimize bone growth and the development of peak bone mass, thereby, lowering the risk for future osteoporotic fractures3,8,9,14–17.

One of the factors that induces bone loss is a reduction of locomotor activity11. Certainly, previous studies have reported a decrease in locomotor activity associated with an increase in stress12. However, locomotor activity is not considered to be a significant factor of vertebral bone loss in murine models13. Moreover, in our study, bone loss in the third lumbar vertebra was comparable to the loss in the long bones of the hind limbs, indicative that the increase in glucocorticoid levels was the main factor inducing bone loss in our model.

Occlusal disharmony was induced by increasing occlusal height. The resultant increase in serum corticosterone level led to a reduction in both cortical and trabecular bone mass of the long bones of the hind limb. In our previous models of osteopenia, including mice fed with a low-calcium diet, we reported a significant reduction in trabecular bone within the first week, with the cortical bone being less affected by the interventions20,21. In comparison to these previous models of osteopenia, the stress induced by occlusal disharmony appears to exert a more severe effect on bone metabolism, with both cortex-related and trabecular indices being significantly decreased. The reduction in the mechanical strength of long bones, which is known to be proportionally correlated to cortical bone-related parameters22, confirmed the severe changes in bone metabolism in the occlusal disharmony model.

Our histomorphometric analyses showed that occlusal disharmony-induced stress reduced bone mass in the long bones of the hind limbs of mice through a decrease in bone formation parameters. Specifically, serum levels of systemic metabolic markers were significantly lower in the disharmony group than in the control group (p < 0.0001), indicative of a decrease in bone formation parameters, but without an increase in bone resorption parameters (Figs 5–7), which was consistent with the findings of previous studies that have evaluated the effects of glucocorticoids in rodents23–25. Some previous studies, however, have reported an effect of glucocorticoids on bone resorption26–28. We examined bone resorption markers in the middle of the experimental period of observation. The serum level of TRACP 5b, which is indicative of bone resorption activity, did increase significantly in the disharmony group on post-induction day 5 (Supplementary Fig. S4b). We also examined the expression levels of Rankl, Opg, Dkk1 and Sost mRNA expression in the tibia and observed a trend to increasing levels in the Rankl/Opg mRNA expression ratio, with decreasing levels in the Dkk1 and Sost mRNA expression ratio, on post-induction day 5 (Supplementary Figs S6 and S7). Furthermore, histopathological examination of cortical bone in the femur was indicative of a high turnover rate of bone remodelling in the middle of the observation period (Supplementary Figs S3 and S4).

In conclusion, occlusal disharmony-induced stress could decrease bone formation and increase bone resorption, leading to osteopenia and reduced mechanical strength of bones, through its effect in increasing serum glucocorticoid levels. To our knowledge, this is the first report to have addressed the possible pathological effects of occlusal disharmony-induced stress on the bone mass and mechanical strength.

Methods

Animals

Five-week-old male C57BL/6J mice were obtained from Sankyo Labo Service Co., Ltd. (Tokyo, Japan). Mice were maintained in our animal care facility under room temperature (21 ± 1 °C), with a 12-h light/12-h dark cycle. The experimental procedures were reviewed and approved by the Institutional Animal Care and Use Committee of the Tokyo Medical and Dental University (Tokyo, Japan, approved number; #0130279A) and all experiments were performed in accordance with relevant guidelines and regulations. Since the mice in the occlusal disharmony group could not easily eat the standard (pellet) diet, the standard diet was changed to a powdered diet on the third day after the standard diet was provided. The mice had three- and six-day acclimation periods, respectively, to adapt to the powdered diet and single cages prior to the experimental intervention (day 0; Fig. 1).

Mice were randomly divided into two groups: a control group (n = 5) and an occlusal disharmony (disharmony) group (n = 5). In the disharmony group, the occlusal height was increased by 0.5 mm, using a composite resin (MI FIL, GC Co. Ltd., Tokyo, Japan), with the mice under anaesthesia, as per methods that have previously been described, but with some modifications2,3 (Fig. 1). The mice were subjected to anaesthesia using medetomidine hydrochloride (0.5 mg/kg; Domitor, Meijiseika, Tokyo, Japan) and ketamine hydrochloride (50 mg/kg; Ketalar, Sankyo, Tokyo, Japan). The same anaesthetic was used in mice in the control group, without any intervention. Atipamezole hydrochloride (the antagonist of medetomidine hydrochloride, 2.5 mg/kg; Nippon Zenyaku Kogyo Co., Ltd., Japan) was administered to all animals to reduce the stress from the anaesthesia29.

Serum corticosterone measurements

The serum was separated from blood samples collected from the orbital vein under anaesthesia on days 1, 3 and day 7 after induction of occlusal disharmony. Each blood sampling procedure was completed within 30 s from the time of contact with a mouse. The separated serum sample was frozen at −80 °C until corticosterone measurements were performed. The serum corticosterone levels were determined using the Corticosterone HS EIA kit (Immunodiagnostic Systems Ltd., UK), according to the manufacturer’s instructions.

Three-dimensional micro-CT analysis

After sacrifice, the tibiae, femurs and the third lumbar vertebrae were dissected, and the soft tissues were roughly removed. Bones were fixed in PBS-buffered glutaraldehyde (0.25%)-formalin (3.7%) solution (pH 7.4) for 2 days at 4 °C, and washed with PBS for radiological analysis.

A desktop X-ray micro-CT system (SMX-100CT, Shimadzu, Kyoto, Japan) was used to investigate the structural changes of the trabecular bone of the lumbar vertebra. The region of interest (ROI) for structural morphometry was the third lumbar vertebra, as shown in Fig. 3a. To separate trabecular bone from the bone marrow, the same threshold level was applied in the three-dimensional image analysis software program (TRI/3-D-BON, Ratoc System Engineering, Tokyo, Japan). The bone volume fraction was measured as the percentage of bone volume per tissue volume (BV/TV, %). Trabecular thickness (Tb.Th, μm), trabecular number (Tb.N, 1/mm), and the trabecular bone pattern factor (TBPf, 1/mm) were also measured.

Bone mineral density measurements

The bone mineral density of the proximal metaphysis of the tibia and the distal- and mid-shaft regions of the femurs were measured by peripheral quantitative computed tomography (pQCT; XCT Research SA + , Stratec Medizintechnik GmbH, Pforzheim, Germany). We also evaluated the strength-strain index (SSI) and torsion index, which provide a measure of bone strength and strength under torsion, respectively22.

Biochemical markers of bone formation/resorption-related parameters

Serum levels of tartrate-resistant acid phosphatase 5b (TRACP 5b) and osteocalcin were analysed using EIA kits (TRACP 5b; MBL CO., LTD, Nagoya-city, Japan, osteocalcin; Takara-Bio Inc, Otsu-city, Japan). The urine carboxy-terminal collagen crosslink (CTX) level was measured using Rat Laps (CTX-I) EIA kit (MBL CO., LTD, Nagoya-city, Japan), according to the manufacturers’ instructions. CTX levels were measured in both groups of mice, before and after occlusal disharmony induction.

Histological assessment

Tibial bones were embedded in glycol methacrylate monomer (GMA). In brief, polymerization was performed at 4 °C. Standard un-decalcified sections (3 μm) were prepared using a fully automated rotary microtome Leica RM2255 device (Leica Biosystems, Nussloch GmbH, Germany). The direction of the cuts made in the bones was guided by μCT images of embedded samples before the sections were made. The sections were then stained with tartrate-resistant acid phosphatase (TRAP) and counterstained with toluidine blue. Histomorphometric analyses were performed using an image analysis system (KS400; Carl Zeiss, Jena, Germany), as per methods previously described30,31.

Bone histomorphometry of the tibial metaphysis

To investigate secondary effects of occlusal disharmony on bone, a standard histomorphometric analysis of the tibial metaphysis was performed using the KS400 image analysing system31–33.

Statistical analysis

The Kolmogorov–Smirnov test was used as a goodness of fit test to confirm the normal distribution of the data. Differences in measured outcomes between the control and disharmony group were evaluated using un-paired Student’s t-tests. A p-value < 0.05 was considered statistically significant.

Electronic supplementary material

Supplementary information (1,015.2KB, pdf)

Acknowledgements

This work was supported by JSPS KAKENHI Grant Number 24890062 and 26861771. We thank Dr. Hiroaki Saito (University Medical Center Hamburg-Eppendorf), Dr. Hitoyata Shimokawa (Department of Pediatric Dentistry, Tokyo Medical and Dental University), and Dr. KEO Preksa (Department of Orthodontic Science, Tokyo Medical and Dental University) for their technical support.

Author Contributions

Y.S. and K.A. designed, organized and performed the experiments, analysed the data, generated the figures, and wrote the manuscript. Y.S. performed the experiments and radiological, histological, and biochemical analyses and drafted the manuscript. M.K. and G.K. performed the experiments and histological analyses. K.A. and T.O. contributed to the helpful discussions, edited the manuscript, and commented on the manuscript. All authors have read and approved the final manuscript.

Competing Interests

The authors declare that they have no competing interests.

Footnotes

Electronic supplementary material

Supplementary information accompanies this paper at 10.1038/s41598-017-18037-y.

Publisher's note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

  • 1.Mori D, Katayama T, Miyake H, Fujiwara S, Kubo K. Occlusal disharmony leads to learning deficits associated with decreased cellular proliferation in the hippocampal dentate gyrus of SAMP8 mice. Neurosci Lett. 2013;534:228–232. doi: 10.1016/j.neulet.2012.12.004. [DOI] [PubMed] [Google Scholar]
  • 2.Yoshihara T, Yawaka Y. Lesions of the ventral ascending noradrenergic bundles decrease the stress response to occlusal disharmony in rats. Neurosci Lett. 2011;503:43–47. doi: 10.1016/j.neulet.2011.08.004. [DOI] [PubMed] [Google Scholar]
  • 3.Yoshihara T, Taneichi R, Yawaka Y. Occlusal disharmony increases stress response in rats. Neurosci Lett. 2009;452:181–184. doi: 10.1016/j.neulet.2009.01.059. [DOI] [PubMed] [Google Scholar]
  • 4.Yoshihara T, Matsumoto Y, Ogura T. Occlusal disharmony affects plasma corticosterone and hypothalamic noradrenaline release in rats. J Dent Res. 2001;80:2089–2092. doi: 10.1177/00220345010800121301. [DOI] [PubMed] [Google Scholar]
  • 5.Carra MC, et al. Prevalence and risk factors of sleep bruxism and wake-time tooth clenching in a 7- to 17-yr-old population. Eur J Oral Sci. 2011;119:386–394. doi: 10.1111/j.1600-0722.2011.00846.x. [DOI] [PubMed] [Google Scholar]
  • 6.Cheifetz AT, Osganian SK, Allred EN, Needleman HL. Prevalence of bruxism and associated correlates in children as reported by parents. J Dent Child. 2005;72:67–74. [PubMed] [Google Scholar]
  • 7.Serra-Negra JM, Paiva SM, Seabra AP, Pordeus IA. Prevalence of sleep bruxism in a group of Brazilian schoolchildren. Eur Arch Paediatr Dent. 2010;11:192–195. doi: 10.1007/BF03262743. [DOI] [PubMed] [Google Scholar]
  • 8.Walker-Bone K. Recognizing and treating secondary osteoporosis. Nat Rev Rheumatol. 2012;8:480–492. doi: 10.1038/nrrheum.2012.93. [DOI] [PubMed] [Google Scholar]
  • 9.Burnham JM. Inflammatory diseases and bone health in children. Curr Opin Rheumatol. 2012;24:548–553. doi: 10.1097/BOR.0b013e328356b0c2. [DOI] [PubMed] [Google Scholar]
  • 10.Yu H, Watt H, Kesavan C, Mohan S. The negative impact of single prolonged stress (SPS) on bone development in mice. Stress. 2013;16:564–570. doi: 10.3109/10253890.2013.806908. [DOI] [PubMed] [Google Scholar]
  • 11.Bourrin S, Palle S, Genty C, Alexandre C. Physical exercise during remobilization restores a normal bone trabecular network after tail suspension-induced osteopenia in young rats. J Bone Miner Res. 1995;10:820–828. doi: 10.1002/jbmr.5650100520. [DOI] [PubMed] [Google Scholar]
  • 12.Sawada T, et al. Reduction in levels of amphiphysin 1 mRNA in the hippocampus of aged rats subjected to repeated variable stress. Neurosci. 2004;126:461–466. doi: 10.1016/j.neuroscience.2004.03.001. [DOI] [PubMed] [Google Scholar]
  • 13.Miyagawa K, et al. A novel underuse model shows that inactivity but not ovariectomy determines the deteriorated material properties and geometry of cortical bone in the tibia of adult rats. J Bone Miner Metab. 2011;29:422–436. doi: 10.1007/s00774-010-0241-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Ondrak KS, Morgan DW. Physical activity, calcium intake and bone health in children and adolescents. Sports Med. 2007;37:587–600. doi: 10.2165/00007256-200737070-00003. [DOI] [PubMed] [Google Scholar]
  • 15.Ruiz JC, Mandel C, Garabedian M. Influence of spontaneous calcium intake and physical exercise on the vertebral and femoral bone mineral density of children and adolescents. J Bone Miner Res. 1995;10:675–682. doi: 10.1002/jbmr.5650100502. [DOI] [PubMed] [Google Scholar]
  • 16.Mølgaard C, Thomsen BL, Michaelsen KF. The influence of calcium intake and physical activity on bone mineral content and bone size in healthy children and adolescents. Osteoporos Int. 2001;12:887–894. doi: 10.1007/s001980170042. [DOI] [PubMed] [Google Scholar]
  • 17.Courteix D, Jaffré C, Lespessailles E, Benhamou L. Cumulative effects of calcium supplementation and physical activity on bone accretion in premenarchal children: a double-blind randomised placebo-controlled trial. Int J Sports Med. 2005;26:332–338. doi: 10.1055/s-2004-821040. [DOI] [PubMed] [Google Scholar]
  • 18.Voorhees JL, Powell ND, Moldovan L, Mo X, Eubank TD, Marsh CB. Chronic restraint stress upregulates erythropoiesis through glucocorticoid stimulation. PLoS One. 2013;8:e77935. doi: 10.1371/journal.pone.0077935. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Seto H, Aoki K, Kasugai S, Ohya K. Trabecular bone turnover, bone marrow cell development, and gene expression of bone matrix proteins after low calcium feeding in rats. Bone. 1999;25:687–695. doi: 10.1016/S8756-3282(99)00229-X. [DOI] [PubMed] [Google Scholar]
  • 20.Aoki K, et al. A TNF receptor loop peptide mimic blocks RANK ligand-induced signaling, bone resorption, and bone loss. J Clin Invest. 2006;116:1525–1534. doi: 10.1172/JCI22513. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Sato K, et al. Regulation of osteoclast differentiation and function by the CaMK-CREB pathway. Nat Med. 2006;12:1410–1416. doi: 10.1038/nm1515. [DOI] [PubMed] [Google Scholar]
  • 22.Ferretti JL. Perspectives of pQCT technology associated to biomechanical studies in skeletal research employing rat models. Bone. 1995;17:353S–364S. doi: 10.1016/8756-3282(96)87956-7. [DOI] [PubMed] [Google Scholar]
  • 23.Lin S, et al. Glucocorticoid-induced osteoporosis in growing rats. Calcif Tissue Int. 2014;95:362–373. doi: 10.1007/s00223-014-9899-7. [DOI] [PubMed] [Google Scholar]
  • 24.Takahashi M, et al. Dosing-time dependent effect of dexamethasone on bone density in rats. Life Sci. 2010;86:24–29. doi: 10.1016/j.lfs.2009.10.020. [DOI] [PubMed] [Google Scholar]
  • 25.Jia D, O’Brien CA, Stewart SA, Manolagas SC, Weinstein RS. Glucocorticoids act directly on osteoclasts to increase their life span and reduce bone density. Endocrinology. 2006;147:5592–5599. doi: 10.1210/en.2006-0459. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.King CS, Weir EC, Gundberg CW, Fox J, Insogna KL. Effects of continuous glucocorticoid infusion on bone metabolism in the rat. Calcif Tissue Int. 1996;59:184–191. doi: 10.1007/s002239900107. [DOI] [PubMed] [Google Scholar]
  • 27.Takuma A, Kaneda T, Sato T, Ninomiya S, Kumegawa M, Hakeda Y. Dexamethasone enhances osteoclast formation synergistically with transforming growth factor-beta by stimulating the priming of osteoclast progenitors for differentiation into osteoclasts. J Biol Chem. 2003;278:44667–44674. doi: 10.1074/jbc.M300213200. [DOI] [PubMed] [Google Scholar]
  • 28.Kaji H, Sugimoto T, Kanatani M, Nishiyama K, Chihara K. Dexamethasone stimulates osteoclast-like cell formation by directly acting on hemopoietic blast cells and enhances osteoclast-like cell formation stimulated by parathyroid hormone and prostaglandin E2. J Bone Miner Res. 1997;12:7334–741. doi: 10.1359/jbmr.1997.12.5.734. [DOI] [PubMed] [Google Scholar]
  • 29.Nakachi H, et al. A structural modulator of tumor necrosis factor type 1 receptor promotes bone formation under lipopolysaccharide-induced inflammation in a murine tooth extraction model. Eur J Pharmacol. 2012;679:132–138. doi: 10.1016/j.ejphar.2011.12.046. [DOI] [PubMed] [Google Scholar]
  • 30.Masud-Khan AA, et al. The local administration of TNF-α and RANKL antagonist peptide promotes BMP-2-induced bone formation. J Oral Biosci. 2013;55:47–54. doi: 10.1016/j.job.2012.12.005. [DOI] [Google Scholar]
  • 31.Kato G, et al. The inhibitory effects of a RANKL-binding peptide on articular and periarticular bone loss in a murine model of collagen-induced arthritis: a bone histomorphometric study. Arthritis Res Ther. 2015;12:251. doi: 10.1186/s13075-015-0753-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Saito H, et al. A tumor necrosis factor receptor loop peptide mimic inhibits bone destruction to the same extent as anti-tumor necrosis factor monoclonal antibody in murine collagen-induced arthritis. Arthritis Rheum. 2007;56:1164–1174. doi: 10.1002/art.22495. [DOI] [PubMed] [Google Scholar]
  • 33.Dempster DW, et al. Standardized nomenclature, symbols, and units for bone histomorphometry: a 2012 update of the report of the ASBMR Histomorphometry Nomenclature Committee. J Bone Miner Res. 2013;28:2–17. doi: 10.1002/jbmr.1805. [DOI] [PMC free article] [PubMed] [Google Scholar]

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