Skip to main content
Download PDF

Intermittent PTH administration improves alveolar bone formation in type 1 diabetic rats with periodontitis

Journal of Translational Medicine volume 16, Article number: 70 (2018) Cite this article

Abstract

Background

Periodontitis is an infectious disease that manifests as alveolar bone loss surrounding the roots of teeth. Diabetes aggravates periodontitis-induced alveolar bone loss via suppression of bone formation. Intermittent parathyroid hormone (PTH) administration displays an anabolic effect on bone. In this study, we investigated the effect of intermittent PTH administration on alveolar bone loss in type 1 diabetic rats with periodontitis.

Methods

Rats were divided into control (C), periodontitis (P), periodontitis treated with PTH (P + PTH), diabetes with periodontitis (DP), and diabetes with periodontitis treated with PTH (DP + PTH) groups. To induce type 1 diabetes, rats were injected with streptozotocin and periodontitis was induced bilaterally by applying ligatures to the mandibular first molars for 30 days. During the experimental period, the P + PTH and DP + PTH groups were subcutaneously injected with PTH (40 μg/kg) three times per week, whereas the C, P, and DP groups were injected with citrate buffer. To observe the mineralization of the alveolar bone, the DP and DP + PTH groups were injected with calcein on days 10 and 27, and with alizarin red on day 20. Thirty days after ligation, histological findings and fluorescence labeling were analyzed in the furcations of the mandibular first molars. Sclerostin-positive osteocytes were assessed by immunohistochemical analyses.

Results

The DP groups had smaller areas of alveolar bone than the other groups, and the DP + PTH group had a larger alveolar bone area than the DP group. The DP group had less osteoid formation than the C group, whereas the DP + PTH had greater osteoid formation than the DP group. Fluorescence labeling results revealed that the DP + PTH group had more mineral deposition on the alveolar bone than the DP group. The DP + PTH group exhibited lower percentage of sclerostin-positive osteocytes in alveolar bone than the DP group.

Conclusions

Intermittent PTH administration diminishes alveolar bone loss and sclerostin expression in osteocytes, but increases osteoid formation and mineralization, suggesting that intermittent PTH administration attenuates diabetes-aggravated alveolar bone loss by the induction of bone formation. PTH-induced bone formation may be related to the regulation of osteocytic sclerostin expression in type 1 diabetic rats with periodontitis.

Background

Parathyroid hormone (PTH), which is synthesized by the parathyroid glands, plays a role in the maintenance of blood calcium levels [1]. Preosteoblasts, osteoblasts, bone-lining cells, and osteocytes express PTH receptors [1]. PTH controls calcium homeostasis via the stimulation of bone remodeling: This process is accomplished by direct effects on osteocytes and osteoblasts, and indirect effects on osteoclasts via its actions on osteocytes and osteoblasts [1]. Although PTH induces both bone resorption and bone formation, its effects are dependent on the frequency of PTH exposure [1]. Continuous and intermittent PTH administration causes catabolic and anabolic effects on bone, respectively [1,2,3]. PTH-mediated anabolic effects are related to the direct action of PTH on osteoblasts and osteocytes. In osteoblasts, intermittent PTH administration promotes osteoblastogenesis, reduces osteoblast apoptosis, and reactivates quiescent bone-lining cells [1, 4, 5]. In an osteocyte cell line, PTH was shown to reduce sclerostin expression [6]. Sclerostin is mainly expressed by osteocytes, inhibiting Wnt binding to low-density lipoprotein receptor-related protein 5/6 and subsequently decreasing bone formation [7,8,9]. The suppression of sclerostin expression induced by intermittent PTH administration has been demonstrated in the calvaria of the mice [10].

Periodontitis is an infectious disease induced by periodontopathogens; it causes the loss of alveolar bone surrounding the roots of teeth and is a common cause of tooth loss [11]. Alveolar bone loss is induced by an acceleration of bone resorption and an attenuation of bone formation [11]. Placing ligatures around teeth induces periodontitis in rats, modeling alveolar bone loss [12,13,14]. Systemic intermittent PTH administration during the maintenance of ligature placement was shown to block alveolar bone loss [12]. The topical intermittent application of PTH in gingiva after the removal of ligatures was shown to recover alveolar bone loss and increase osteoid formation on the alveolar bone surface [13]. These findings suggest an anabolic effect of intermittent PTH administration on alveolar bone in rats with periodontitis.

Systemic diseases such as osteoporosis and diabetes are risk factors for periodontitis [15, 16]. In ovariectomized rats with periodontitis, intermittent PTH administration was shown to reduce alveolar bone loss [17]. PTH-mediated anabolic effects on bone were observed in tibiae and alveolar bone of type 1 diabetic animals [18, 19]. However, the effects of PTH on alveolar bone formation and osteocytic sclerostin expression of rats with both periodontitis and type 1 diabetes have been not determined. Therefore, we investigated the anabolic effects of intermittent PTH administration in rats with streptozotocin (STZ)-induced type 1 diabetes accompanied by periodontitis.

Methods

Animal experiments

After acclimation for 1 week, the F344 male rats (Japan SLC, Inc., Hamamatsu, Shizuoka, Japan) were divided into five groups: control (C, N = 10), periodontitis (P, N = 7), periodontitis treated with PTH (P + PTH, N = 7), diabetes with periodontitis (DP, N = 6), and diabetes with periodontitis treated with PTH (DP + PTH, N = 6). The experimental protocol is presented in Fig. 1a. After fasting for 18 h, both diabetes groups were intravenously injected with STZ (50 mg/kg in 0.1 M citrate buffer, Sigma-Aldrich, St. Louis, MO, USA) and the non-diabetes groups were injected with citrate buffer alone. On day 7 after injection, blood was obtained from the tail vein, and glucose levels were measured using an Accu-Check active system (Roche, Mannheim, Germany) under fasting conditions. Rats with a blood glucose level greater than 300 mg/dl were considered diabetes. Rats were then anesthetized with zoletil 50 (30 mg/kg; Virbac, Carros, France) and rompun (10 mg/kg; Bayer Korea, Ansan, Gyenoggi-do, Korea), and periodontitis was induced bilaterally by placing dental floss around the cervixes of the first mandibular molars. During 30 days after the induction of periodontitis, the P + PTH and DP + PTH groups were subcutaneously given PTH three times per week (40 μg/kg, Bachem, Torrance, CA, USA). PTH was administered 4 h before both the placement of the ligatures (day 0) and the time of sacrifice (day 30). During the experimental period, body weights and fasting glucose levels were measured to ensure maintenance of diabetes. The animal protocols were approved by the Institutional Animal Care and Use Committee of Yonsei University (Approval Number: 2015-0345).

Fig. 1
figure 1

Experimental protocol for intermittent PTH administration and changes in body weights and fasting glucose levels during the experimental period. Rats were divided into five groups: C, P, P + PTH, DP, and DP + PTH. a Experimental protocol: on 1 week after induction of diabetes by STZ, periodontitis was induced by placing bilateral ligatures around the mandibular first molars using dental floss. After placement of the ligatures, the DP and DP + PTH groups were given intraperitoneal injections of calcein (10 mg/kg) on days 10 and 27, and alizarin red (20 mg/kg) on day 20, respectively. During 30 days after the induction of periodontitis, the P + PTH and DP + PTH groups were subcutaneously administered PTH three times per week (40 μg/kg). On days 0 and 30, PTH was administered 4 h before both placement of the ligatures and the time of sacrifice, respectively. b Body weights in each group and c Fasting glucose levels in each group. Data are presented as the mean ± SE. *P < 0.05 compared with the C group

Full size image

Histological analysis of bone loss and bone formation

For histological analysis, the left mandibles and tibiae were fixed in 10% neutral-buffered formalin overnight. The mandibles were decalcified in 10% ethylenediaminetetraacetic acid (EDTA) for 2 months. Serial sagittal sections (4-μm-thick) were cut from paraffin-embedded tissue blocks. The sections with clear dental pulp of the mesial and distal roots of the first molars were selected and stained with hematoxylin and eosin (H&E). Slides were scanned using a Aperio AT2 Digital Whole Slide scanner (Leica Microsystems Inc., Buffalo Grove, IL, USA) and analyzed using Aperio ImageScope software (version12.3.2.2013, Aperio Technologies Inc., Vista, CA, USA). The degree of alveolar bone loss in the furcation of the first molar was estimated by measuring the percentage of the alveolar bone to the region of interest (ROI) in the furcation. The ROI for alveolar bone loss extended 0.8 mm from the top of the furcation. To determine bone formation, the osteoid region of the ROI in the furcation was measured, as previously described [20]. The ROI for bone formation extended 0.5 mm from the remaining alveolar bone crest (ABC) in the furcation. The tibiae of the DP and DP + PTH groups were decalcified in 10% EDTA for 1 month. Tibial sections appearing proximal epiphysial growth plate were selected and then stained with H&E.

Fluorescence calcein and alizarin red labeling

To analyze bone mineralization, calcein and alizarin red fluorochromes, which bind calcium in the mineralized areas of the bone, were injected into the DP and DP + PTH groups [21]. After placement of the ligatures around the teeth as described above, the DP and DP + PTH groups were given an intraperitoneal injection of calcein (10 mg/kg, Sigma-Aldrich, St Louis, MO, USA) on days 10 and 27, and alizarin red (20 mg/kg, Sigma-Aldrich, St Louis, MO, USA) on day 20, respectively. On day 30 after placement of the ligatures, the right mandibles and tibiae were fixed in 10% neutral-buffered formalin and dehydrated in a graded series of ethanol solutions. The molar regions of the mandibles were embedded in methyl methacrylate-based resin and cut into 200-μm-thick sections (Struers, Germany). The sections were polished to obtain 50-μm slices using a hard tissue grinding system (EXAKT, Germany). Calcein and alizarin red labeling was observed in alveolar bone within the furcation of the first molars and trabecular bone under the epiphyseal growth plate of the tibiae by confocal laser scanning microscopy (LSM 700, Zeiss, Göttingen, Germany).

Immunohistochemical analyses of sclerostin expression

For sclerostin staining, sections of alveolar bone were deparaffinized and rehydrated through a series of graded ethanol solutions. To inhibit endogenous peroxidase activity, sections were quenched in 3% H2O2 for 20 min and then treated with trypsin (Thermo Fisher Scientific, Waltham, MA, USA) for antigen retrieval. Immunohistochemistry was carried out using universal kits (Vector Laboratories, Burlingame, CA, USA) according to the manufacturer’s instructions. Sections were preincubated with normal horse blocking solution for 20 min and then incubated overnight at 4 °C with goat anti-sclerostin antibody (1:300 dilution, R&D Systems, Minneapolis, MN, USA). Sections were developed using the 3,3′-diaminobenzidine chromogen and counterstained with methyl green. Slides were scanned using a Aperio AT2 Digital Whole Slide scanner (Leica Microsystems Inc., Buffalo Grove, IL, USA) and analyzed using Aperio ImageScope software (version12.3.2.2013, Aperio Technologies Inc., Vista, CA, USA). Numbers of sclerostin-positive osteocytes were counted in the ROI, which extended 0.5 mm from the ABC in the furcations of the first molars, and are presented as the percentage of sclerostin-positive osteocytes per number of total osteocytes in the ROI.

Statistical analysis

All statistical analyses were performed using a statistical analysis program (SPSS, Chicago, IL, USA). One-way analysis of variance followed by Scheffé’s method was used to determine significant differences. A value P < 0.05 was considered statistically significant. Data are expressed as the mean ± standard error (SE).

Results

Effects of PTH on body weights and fasting blood glucose levels

During the experimental period, C, P, and P + PTH groups showed a gradual increase in body weights, but the DP and DP + PTH groups maintained body weights (Fig. 1b). Fasting blood glucose levels of the C, P, and P + PTH groups were about 100 mg/dl and were maintained during the experimental period (Fig. 1c). However, fasting blood glucose levels of the DP and DP + PTH groups were greater than 300 mg/dl. There was no difference in body weights and fasting glucose levels between the DP and DP + PTH groups.

Effects of PTH on alveolar bone loss and bone formation

To estimate the effects of PTH on alveolar bone loss, the alveolar bone areas in the furcations of the first molars were measured (Fig. 2a). The alveolar bone areas of the P, P + PTH, DP, and DP + PTH groups were lower than the corresponding area in the C group. Interestingly, the DP + PTH group had more alveolar bone than did the DP group. To evaluate the effects of PTH on new bone formation in alveolar bone, the osteoid region was estimated in the furcations of the first molars (Fig. 2b). While the osteoid area was larger in the P, P + PTH, and DP + PTH groups than in the C group, it was smaller in the DP group. Both the P and P + PTH groups had the larger osteoid areas than did the DP and DP + PTH groups. The DP + PTH group had the greater osteoid area than the DP group. Calcein- and alizarin red-labeled bone areas were larger in the DP + PTH group than in the DP group (Fig. 2c).

Fig. 2
figure 2

The effects of intermittent PTH administration on alveolar bone loss and bone formation in the furcations. a Representative images of the alveolar bone area in each group (left panels; H&E stain; scale bar = 100 μm). Measurements of the alveolar bone area in each group (right panel). b Measurements of the osteoid area in each group. c Representative images of labeled alveolar bone surfaces by calcein and alizarin red fluorescence in the DP and DP + PTH groups (scale bar = 100 μm). Data are presented as the mean ± SE. *P < 0.05 compared with the C group. #P < 0.05. AB alveolar bone; BM bone marrow, PDL periodontal ligament

Full size image

Effects of PTH on tibial bone loss and bone formation

To confirm the anabolic effects of PTH on other bone, trabecular bone in the tibiae was observed by H&E staining and fluorescence labeling. The DP + PTH group showed more trabecular bone than the DP group by H&E staining (Fig. 3a), and the DP + PTH group showed a larger calcein- and alizarin red-labeled area in trabecular bone than the DP group (Fig. 3b).

Fig. 3
figure 3

The effects of intermittent PTH administration in tibiae. a Representative images of trabecular bone in tibiae of the DP and DP + PTH groups (H&E stain; scale bar = 100 μm). b Representative images of labeled trabecular bone surfaces by calcein and alizarin red fluorescence in the DP and DP + PTH groups (scale bar = 100 μm)

Full size image

Effects of PTH on sclerostin expression in alveolar bone

To estimate the effects of PTH on sclerostin expression in alveolar bone, sclerostin-positive osteocytes were counted in the furcations of the first molars (Fig. 4). The percentage of sclerostin-positive osteocytes was greater in the DP group than in the other groups. While that of DP + PTH group was lower than in the DP group, it was higher than in the P + PTH group.

Fig. 4
figure 4

The effects of intermittent PTH administration on osteocytic sclerostin expression in alveolar bone. Representative images of sclerostin-positive osteocytes in the DP and DP + PTH groups. White and red arrowheads indicate representative sclerostin-negative and -positive osteocytes, respectively (upper panels; immunohistochemistry; scale bar = 100 μm). Percentage of sclerostin-positive osteocytes in each group (lower panel). Data are presented as the mean ± SE. *P < 0.05 compared with the C group. #P < 0.05

Full size image

Discussion

The frequency of PTH administration required to elevate PTH levels intermittently varies from daily to a few times per week. Daily PTH administration increases osteoblast number and bone formation in rat tibiae, whereas continuous PTH infusion via an osmotic pump results in systemic effects, including bone resorption and bone marrow fibrosis, suggesting that intermittent PTH administration is required for the anabolic effects of this hormone [2]. In both rats with periodontitis and ovariectomized rats with periodontitis, anabolic effects on alveolar bone were induced by PTH administration three times per week for 1 month [12, 17]. Based on the data generated by these two groups, we administered PTH three times per week for 1 month in type 1 diabetic rats with periodontitis. PTH administration in periodontitis condition did not result in a significant increase in the area of the alveolar bone compared to the P group, but PTH administration in periodontitis with diabetes condition elicited its improvement compared to the DP group. These findings suggest that intermittent PTH administration may attenuate diabetes-aggravated alveolar bone loss in type 1 diabetic rats with periodontitis. A study of PTH-treated ovariectomized rats with periodontitis (three times per week) showed recovery of alveolar bone loss to levels of normal rats [17]; these results are inconsistent to our findings, where alveolar bone loss in the DP + PTH group did not recover to levels of the C group. The characteristics of systemic diseases related to bone loss might contribute to differences in the level of protection against alveolar bone loss. Additionally, daily PTH administration in mice with type 1 diabetes caused an elevation of trabecular bone density in the tibiae to levels of normal mice [18]. To improve rates of bone protection in cases of type 1 diabetes with periodontitis after PTH administration, the optimal therapeutic strategy considering bone type in PTH administration might be considered.

Bone loss was determined by the level of bone formation. As in study of rats with periodontitis treated intermittently with PTH [13], we also found greater osteoid area in alveolar bone of the DP + PTH group compared to the DP group. In addition, mineral deposition in alveolar bone was greater in the DP + PTH group than in the DP group, suggesting an anabolic effect of PTH on alveolar bone in type 1 diabetic rats with periodontitis. In long bones of type 1 diabetic mice, daily PTH administration increased trabecular bone density accompanied by increased mineral apposition and an increase in the number of osteoblasts lining the bone surface [18]. In our study, tibiae of the DP + PTH group had an increase in trabecular bone and mineral deposition compared with the DP group. These findings suggest that PTH has similar anabolic effects on trabecular bone (e.g., the tibia) as on alveolar bone in type 1 diabetes.

In previous studies of rats with periodontitis, treatment with sclerostin antibodies was found to induce an anabolic response during alveolar bone healing by increasing bone formation [15, 22]. Sclerostin in osteocytes is proposed to be a target gene of PTH in vivo [1, 6, 10]. Daily PTH administration has been shown to increase osteoblast activity in normal mice, with no effects in mice lacking PTH receptors in osteocytes [23]. In addition, a single PTH administration was shown to decrease the number of sclerostin-positive osteocytes in vertebral trabecular bone in normal mice but failed to suppress the number of sclerostin-positive osteocytes in mice lacking PTH receptors [23]. These results suggest that osteocytes play a significant role in the anabolic effects of intermittent PTH administration. A single PTH administration was found to induce a transient decline in sclerostin mRNA levels in mice vertebrae and rat femurs [6, 10]. Daily PTH administration for 2 months was found to induce a steady decline in sclerostin mRNA levels in femurs of estrogen-deprived rats, suggesting that inhibition of sclerostin is sustained by long-term intermittent PTH administration [10]. In this study, more sclerostin-positive osteocytes were observed in the DP group compared to the C group. There was no significant difference in sclerostin expression in the P + PTH group compared to the P group, but sclerostin expression was lower in the DP + PTH group compared to the DP group. Our results suggest that PTH may have an inhibitory effect on the induction of sclerostin expression in alveolar bone by diabetes similar to results seen in a study of estrogen-deprived rats treated with PTH [10]. Taken together, decreased sclerostin expression in osteocytes after intermittent PTH administration appears to be involved in the increase in bone formation observed in type 1 diabetic rats with periodontitis.

Conclusions

In summary, these results indicate that intermittent PTH administration increases osteoid formation and mineralization, and diminishes alveolar bone loss and sclerostin expression in osteocytes of type 1 diabetic rats with periodontitis. Therefore, intermittent PTH administration may improve bone formation and attenuate diabetes-aggravated bone loss by decreasing sclerostin expression in osteocytes of type 1 diabetic rats with periodontitis.

Abbreviations

ABC:

alveolar bone crest

C:

control

DP:

diabetes with periodontitis

DP + PTH:

diabetes with periodontitis treated with PTH

EDTA:

ethylenediaminetetraacetic acid

H&E:

hematoxylin and eosin

N:

number

P:

periodontitis

P + PTH:

periodontitis treated with PTH

PTH:

parathyroid hormone

ROI:

the region of interest

SE:

standard error

STZ:

streptozotocin

References

  1. Silva BC, Bilezikian JP. Parathyroid hormone: anabolic and catabolic actions on the skeleton. Curr Opin Pharmacol. 2015;22:41–50.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  2. Dobnig H, Turner RT. The effects of programmed administration of human parathyroid hormone fragment (1–34) on bone histomorphometry and serum chemistry in rats. Endocrinology. 1997;138:4607–12.

    Article  CAS  PubMed  Google Scholar 

  3. Silva ED, Vasconcelos DF, Marques MR, Silva MA, Manzi FR, Barros SP. Intermittent administration of parathyroid hormone improves the repairing process of rat calvaria defects: a histomorphometric and radiodensitometric study. Med Oral Patol Oral Cir Bucal. 2015;20:e489–93.

    Article  PubMed  PubMed Central  Google Scholar 

  4. Kim SW, Pajevic PD, Selig M, Barry KJ, Yang JY, Shin CS, Baek WY, Kim JE, Kronenberg HM. Intermittent parathyroid hormone administration converts quiescent lining cells to active osteoblasts. J Bone Miner Res. 2012;27:2075–84.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  5. Jilka RL. Molecular and cellular mechanisms of the anabolic effect of intermittent PTH. Bone. 2007;40:1434–46.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Bellido T, Ali AA, Gubrij I, Plotkin LI, Fu Q, O’Brien CA, Manolagas SC, Jilka RL. Chronic elevation of parathyroid hormone in mice reduces expression of sclerostin by osteocytes: a novel mechanism for hormonal control of osteoblastogenesis. Endocrinology. 2005;146:4577–83.

    Article  CAS  PubMed  Google Scholar 

  7. Poole KE, van Bezooijen RL, Loveridge N, Hamersma H, Papapoulos SE, Lowik CW, Reeve J. Sclerostin is a delayed secreted product of osteocytes that inhibits bone formation. FASEB J. 2005;19:1842–4.

    Article  CAS  PubMed  Google Scholar 

  8. Bellido T, Saini V, Pajevic PD. Effects of PTH on osteocyte function. Bone. 2013;54:250–7.

    Article  CAS  PubMed  Google Scholar 

  9. Delgado-Calle J, Sato AY, Bellido T. Role and mechanism of action of sclerostin in bone. Bone. 2017;96:29–37.

    Article  CAS  PubMed  Google Scholar 

  10. Keller H, Kneissel M. SOST is a target gene for PTH in bone. Bone. 2005;37:148–58.

    Article  CAS  PubMed  Google Scholar 

  11. Graves DT, Li J, Cochran DL. Inflammation and uncoupling as mechanisms of periodontal bone loss. J Dent Res. 2011;90:143–53.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  12. Barros SP, Silva MA, Somerman MJ, Nociti FH Jr. Parathyroid hormone protects against periodontitis-associated bone loss. J Dent Res. 2003;82:791–5.

    Article  CAS  PubMed  Google Scholar 

  13. Tokunaga K, Seto H, Ohba H, Mihara C, Hama H, Horibe M, Yoneda S, Nagata T. Topical and intermittent application of parathyroid hormone recovers alveolar bone loss in rat experimental periodontitis. J Periodontal Res. 2011;46:655–62.

    Article  CAS  PubMed  Google Scholar 

  14. Lee DE, Kim JH, Choi SH, Cha JH, Bak EJ, Yoo YJ. Periodontitis mainly increases osteoclast formation via enhancing the differentiation of quiescent osteoclast precursors into osteoclasts. J Periodontal Res. 2015;50:256–64.

    Article  CAS  PubMed  Google Scholar 

  15. Chen H, Xu X, Liu M, Zhang W, Ke HZ, Qin A, Tang T, Lu E. Sclerostin antibody treatment causes greater alveolar crest height and bone mass in an ovariectomized rat model of localized periodontitis. Bone. 2015;76:141–8.

    Article  CAS  PubMed  Google Scholar 

  16. Toker H, Ozdemir H, Balci H, Ozer H. N-acetylcysteine decreases alveolar bone loss on experimental periodontitis in streptozotocin-induced diabetic rats. J Periodontal Res. 2012;47:793–9.

    Article  CAS  PubMed  Google Scholar 

  17. Marques MR, da Silva MA, Manzi FR, Cesar-Neto JB, Nociti FH Jr, Barros SP. Effect of intermittent PTH administration in the periodontitis-associated bone loss in ovariectomized rats. Arch Oral Biol. 2005;50:421–9.

    Article  CAS  PubMed  Google Scholar 

  18. Motyl KJ, McCauley LK, McCabe LR. Amelioration of type I diabetes-induced osteoporosis by parathyroid hormone is associated with improved osteoblast survival. J Cell Physiol. 2012;227:1326–34.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  19. Zhang W, Wu SZ, Zhou J, Chen HM, Gong YL, Peng FF, Zhang BF. Parathyroid hormone-related peptide (1–34) reduces alveolar bone loss in type 1 diabetic rats. Arch Oral Biol. 2017;83:13–9.

    Article  CAS  PubMed  Google Scholar 

  20. Kim JH, Lee DE, Choi SH, Cha JH, Bak EJ, Yoo YJ. Diabetic characteristics and alveolar bone loss in streptozotocin- and streptozotocin-nicotinamide-treated rats with periodontitis. J Periodontal Res. 2014;49:792–800.

    Article  CAS  PubMed  Google Scholar 

  21. Barros SP, Arce RM, Galloway P, Lawter R, Offenbacher S. Therapeutic effect of a topical CCR2 antagonist on induced alveolar bone loss in mice. J Periodontal Res. 2011;46:246–51.

    Article  CAS  PubMed  Google Scholar 

  22. Taut AD, Jin Q, Chung JH, Galindo-Moreno P, Yi ES, Sugai JV, Ke HZ, Liu M, Giannobile WV. Sclerostin antibody stimulates bone regeneration after experimental periodontitis. J Bone Miner Res. 2013;28:2347–56.

    Article  CAS  PubMed  Google Scholar 

  23. Saini V, Marengi DA, Barry KJ, Fulzele KS, Heiden E, Liu X, Dedic C, Maeda A, Lotinun S, Baron R, Pajevic PD. Parathyroid hormone (PTH)/PTH-related peptide type 1 receptor (PPR) signaling in osteocytes regulates anabolic and catabolic skeletal responses to PTH. J Biol Chem. 2013;288:20122–34.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

Download references

Authors’ contributions

JHK participated in the establishment of the animal model and drafted the manuscript. ARK participated in the establishment of the animal model and histological analysis. YHC participated in the analysis using confocal microscopy. AK participated in histological analysis. YS participated in the monitoring of blood glucose levels. GHW helped to draft and polish the manuscript. JHC advised on the study design and helped to draft the manuscript. EJB and YJY designed the study and revised the manuscript. All authors read and approved the final manuscript.

Acknowledgements

None.

Competing interests

The authors declare that they have no competing interests.

Availability of data and materials

Please contact author for data requests.

Consent for publication

Not applicable.

Ethics approval and consent to participate

The animal protocols were approved by the Institutional Animal Care and Use Committee of Yonsei University (Approval Number: 2015-0345).

Funding

This research was supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science, ICT and Future Planning (NRF-2014R1A2A1A11049412). This study was supported by the Yonsei University College of Dentistry Fund (6-2016-0015).

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Author information

Author notes

  1. Ji-Hye Kim, Ae Ri Kim, Eun-Jung Bak and Yun-Jung Yoo contributed equally to this work

Authors and Affiliations

  1. Department of Dental Hygiene, Jeonju Kijeon College, Jeonju, Republic of Korea

    Ji-Hye Kim

  2. Department of Oral Biology, Yonsei University College of Dentistry, 134 Sinchon dong, Seodaemun-gu, Seoul, 120-752, Republic of Korea

    Ae Ri Kim, Yun Hui Choi, Aeryun Kim, Jeong-Heon Cha, Eun-Jung Bak & Yun-Jung Yoo

  3. Department of Applied Life Science, The Graduate School, Yonsei University, Seoul, Republic of Korea

    Ae Ri Kim, Jeong-Heon Cha & Yun-Jung Yoo

  4. BK21 PLUS Project, Yonsei University College of Dentistry, Seoul, Republic of Korea

    Ae Ri Kim & Jeong-Heon Cha

  5. DONG-A Pharm, Yongin-si, Gyeonggi-Do, Republic of Korea

    Yongsung Sohn

  6. Department of Clinical Laboratory Science, Semyung University, Jecheon, Republic of Korea

    Gye-Hyeong Woo

  7. Microbiology and Molecular Biology, Key Laboratory of Oral Medicine, Guangzhou Institute of Oral Disease, Stomatology Hospital of Guangzhou Medical University, Guangzhou, China

    Jeong-Heon Cha

Authors
  1. Ji-Hye Kim
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Ae Ri Kim
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Yun Hui Choi
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Aeryun Kim
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Yongsung Sohn
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Gye-Hyeong Woo
    View author publications

    You can also search for this author in PubMed Google Scholar

  7. Jeong-Heon Cha
    View author publications

    You can also search for this author in PubMed Google Scholar

  8. Eun-Jung Bak
    View author publications

    You can also search for this author in PubMed Google Scholar

  9. Yun-Jung Yoo
    View author publications

    You can also search for this author in PubMed Google Scholar

Corresponding authors

Correspondence to Eun-Jung Bak or Yun-Jung Yoo.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Kim, JH., Kim, A.R., Choi, Y.H. et al. Intermittent PTH administration improves alveolar bone formation in type 1 diabetic rats with periodontitis. J Transl Med 16, 70 (2018). https://doi.org/10.1186/s12967-018-1438-2

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12967-018-1438-2

Keywords

Journal of Translational Medicine

ISSN: 1479-5876

Contact us