ALL Metrics
-
Views
-
Downloads
Get PDF
Get XML
Cite
Export
Track
Research Article

Effect of vitamin E supplementation on orthodontic tooth movement in Wistar rats

[version 1; peer review: 1 approved, 1 not approved]
PUBLISHED 04 Sep 2020
Author details Author details
OPEN PEER REVIEW
REVIEWER STATUS

Abstract

Background: Tooth movement induced by the application of orthodontic force is facilitated by bone remodelling cells and chemical mediators. Vitamin E has anti-inflammatory properties, which helps in suppressing the damaging effects of oxygen free radicals in cells during bone formation. This study aimed to evaluate the effect of vitamin E supplementation on orthodontic tooth movement in Wistar rats.
Methods: Wistar rats (n=56) were divided into two groups. Group 1 served as the control groups, while group 2 was given vitamin E for 14 days before application of orthodontic force. Each group was divided into four subgroups (n=7), corresponding to the number of days orthodontic force lasted, i.e. 0, 1, 3, 7 days. At each of these four time points, distance measurements and quantity of osteoblasts-osteoclasts were measured in each rat.
Results: Tooth movement distance was increased for group 2 than group 1 for all time intervals, but this difference was only statistically different on day 3 (p=0.001). For both groups, tooth movement was significantly different between each time interval in each group (p=0.041). The mean number of osteoblast cells was increased for group 2 compared to group 1 for all time intervals (p<0.05), but was not significant different between time intervals (p=0.897). The number of osteoclasts was not significantly different between groups, but it was statistically different between time intervals (p=0.004).
Conclusion: Present outcomes demonstrate that vitamin E contributes to faster tooth movement compared to control group.  It also stimulates more bone formation without reducing the bone resorption.

Keywords

Orthodontic tooth movement, vitamin E, tooth movement distance, osteoblast, osteoclast.

Introduction

Tooth movement is induced by the application of orthodontic force characterized by bone and periodontal tissue remodelling. Orthodontic force also alters periodontal tissue vascularity and blood flow, resulting in the local synthesis and release of various molecules such as neurotransmitters, cytokines, growth factors, colony-stimulating factors and arachidonic acid metabolites1.

Bone remodelling is a process that enables tooth movement. It involves bone-reabsorption by osteoclasts on the pressure site and bone-formation by osteoblasts on the tension site2,3. Osteoclasts are multinucleated cells, irregular in shape with a process originating from Howship’s lacunae4. They stimulate bone resorption by creating cavities in the bone known as lacunae that will be filled by osteoblast cells3. According to Mavragani et al., the cellular process of osteoclast proliferation has been used as important indicators in evaluating the level of tooth movement5. Osteoblasts are mononuclear cells that originate from mesenchymal stem cells in bone marrow. Mature osteoblasts form the osteoid by synthesizing collagen and non-collagen proteins6.

According to Burstone in Asiry’s citation, there are three phases of orthodontic tooth movement, which consists the initial, lag and postlag phases7. The initial stage of orthodontic tooth movement stimulates an inflammatory response involving cells and blood vessels in periodontal ligaments as well as chemical mediators. In response to mechanical stress caused by the application of orthodontic force, substances such as cytokines and enzymes are released2,8. Interleukin-1β is a pro-inflammatory cytokine that facilitates fusion and activation of osteoclasts, and encourages early bone resorption9.

Studies have shown that vitamin E has anti-inflammatory properties, which helps suppress damaging effects of oxygen free radicals in cells during bone formation10. Previous studies carried out by Esenlik et al. and Xu et al. suggest that vitamin E supplementation may alter cytokine production; vitamin E supplement maintains normal bone remodelling in young animals and increases bone mass by decreasing the concentration of free radicals which suppress bone formation11,12.

Since orthodontic tooth movement is facilitated by bone remodelling cells and chemical mediators, it is possible to hypothesize that vitamin E has a positive effect on bone remodelling cells, which is crucial to tooth movement. However, it is unknown if vitamin would accelerate the movement or inhibit tooth movement. The purpose of this study was to evaluate the effect of vitamin E supplementation on orthodontic tooth movement in Wistar rats. Mice and rats are mammals that have a reasonably comparable metabolism to humans, which can be used for biological-cellular mechanism analysis in orthodontic tooth movement13.

Methods

Animals

This article was reported in line with the ARRIVE guidelines. The study was an in-vivo quasi experiment, which was approved by the Animal Research Ethics Committee, Department of Biology - Faculty of Mathematics and Science, Universitas Sumatera Utara (No. 0128/KEPH-FMIPA/2019).

A total of 56 healthy male, four to five-months old, Wistar rats, weighing 150–250 grams, were used in this study. The Wistar Rats came from the same breeding farm (Deli Serdang, North Sumatera, Indonesia) in two cycles.

The rats were adapted to their environment for 7 days before the experiment start. They were nurtured at the Animal House at Faculty of Mathematics and Science, Universitas Sumatera Utara in polycarbonate cage, which measured 480 mm × 265 mm × 210 mm. Each cage had wood shavings on the floor, and contained 3 or 4 animals, which were marked for each subgroup. Rats were chosen for each group by simple random sampling.

Low light to dark cycle was maintained for a minimum 12 hours at 25–30°C for room temperature within the experiment period. The rats were given a standard pellet diet. All conditions served to produce the optimum condition of the rats’ habitat14. A rubber separator was inserted between maxillae’s incisors to produce non-invasive experiments. Anaesthetic was used to euthanize the rats at the end of the experimental procedure.

Experiment

Wistar rats (n=56) were divided into two groups. Each group was then divided into four subgroups (n=7), corresponding to the number of the days orthodontic force lasted, i.e. 0, 1, 3, 7 days. The sample size of each subgroup was decided by Sastroasmoro and Ismael’s formula for hypothetical analysis between independent variables15.

Subgroups were chosen based on the rats’ social behaviours. Hyperactive rats were chosen to be in the same cage, separately to rats with a more passive behaviour. These conditions avoided any anxiety social-related behaviour between rats in the cage within the experiment. For each experiment, a researcher who was blind to the experiment chose a sample randomly from each cage.

Group 1 were the control group and were given water orally as a placebo. The rats’ tail was marked with black pen. Group 2 were the experimental group and were given vitamin E (dl-α-Tocopheryl Acetate; Sanbe, Indonesia) at a dosage of 60 mg/kg, orally using gavage needle. The group 2 rats’ tail marked with red pen.

Water and vitamin E were given every day at 8am, for 14 days before and continued after application of orthodontic force. After 14 days, orthodontic force was applied to each rat in both groups by addition of a rubber separator to one of the maxilla incisors (Figure 1A). This administration of orthodontic force applied were carried out before daily water and vitamin E feeding. This procedure counted as the baseline time of the experiment. At each of these four time points distance measurements and quantity of osteoblasts-osteoclasts were measured (see section below).

b072f850-67f7-45c8-af76-bf9b7c85818f_figure1.gif

Figure 1.

(A) Rat separator; (B) Distance measurement; (C) Microscopic of whole teeth at 40x magnification. Lines, Yellow=teeth; Green=periodontal ligament; Red=alveolar bone. Arrows, Blue=pressure side; Green=tension side.

At end of each experiment period, the dosage of ketamine® at 80mg/kg of body weight and xyla® (Interchemie, Holland) at 10mg/kg of body weight was used to euthanised each rat by cardiac puncture methods for further research with blood analysis.

Outcomes

Tooth movement was measured using a digital calliper (Mitutoyo, Japan) was used to measure the distance between maxilla incisors at mesial cervical (Moorrees method) immediately after removal of the rubber separator (Figure 1B)16.

The pre-maxillae were dissected and fixated in 10% formalin for 24h, and decalcified with rapid-decalsifier, Nitric acid 10% (Aurona Scientific, Singapore) for 10-14 days. The embedded blocks were trimmed using a Leica microtome (Leica, Germany) into 5µm sections. Histological sections were stained with haematoxylin-eosin and were examined using Olympus CX21 light microscope at 400x magnification to analyse the number of cells within five fields of view for each measurement. A pressured site exhibited as a narrow area between teeth and alveolar bone where the tooth tended to move, and this site was used for osteoclast analysis. A tension site exhibited as a wide area between teeth and alveolar bone where the tooth was left out, and this site was used for osteoblast analysis (Figure 1C).

Statistical analysis

IBM-SPSS (Statistical Package for Social Sciences), version 26.0, was used for statistical analysis. Independent t-test and Mann-Whitney test were used to analyse the difference between the two main groups. General Linear Model-Repeated Measures (ANOVA GLM-RM) and Friedman analysis were used to analyse the difference between time intervals. Significant differences were determined at p<0.05.

Results

Tooth movement distances were greater in group 2 compared to group 1 at each time point (Table 1). This difference was only statistically significant on day 3 (p=0.001). For both groups, tooth movement was significantly different between each time interval in each group (p=0.041). After day 3, movement for group 1 reduced, while for group 2, this continued to increase until day 7.

Table 1. Comparison of tooth movement distance between Group 1 (control) and group 2 (vitamin E treatment) (n=7/subgroup (day)).

Data are presented as mean±SD.

DayTooth movement (mm)P valueaP valueb
Group 1Group 2
00.00±0.000.00±000Baseline0.041
10.25±0.050.31±0.130.486
30.22±0.120.50±0.110.001
70.37±0.200.55±0.220.1373

p<0.05 – statistically significant. aIndependent t-test; bANOVA GLM-RM

The number of osteoblasts in group 2 were higher compared with group 1 at each time point (Figure 2A and B; Table 2). These differences were statistically significant (p<0.05). Group 2 showed increased osteoblasts starting from day 0 to day 3, while group 1 had decreased osteoblast after day 3.

b072f850-67f7-45c8-af76-bf9b7c85818f_figure2.gif

Figure 2. Osteoblasts and osteoclasts in rat alveolar bone at 400x magnification.

(A) osteoblasts in group 1 (control); (B) osteoblasts in group 2 (vitamin E treatment); (C) osteoclasts in group 1; (D) osteoclasts in a Howship’s lacuna in group 2.

Table 2. Comparison of number of osteoblasts between Group 1 (control) and group 2 (vitamin E treatment) (n=7/subgroup (day)).

Data are presented as mean±SD.

DayNumber of osteoblasts (n)P valueaP valueb
Group 1Group 2
05.14±1.349.21±3.210.0120.001
15.29±1.719.36±2.380.003
33.86±1.9410.14±3.530.004
75.04±0.958.43±1.020.002

p<0.05 – statistically significant. a Mann-Whitney test; b Friedman analysis

The number of osteoclasts in group 2 were higher than group 1 except on day 1, but the differences were not significant statistically (Figure 2C and D; Table 3).

Table 3. Comparison of number of osteoclasts between Group 1 (control) and group 2 (vitamin E treatment) (n=7/subgroup (day)).

Data are presented as mean±SD.

DayNumber of osteoclasts (n)P valueaP valueb
Group 1Group 2
00.89±0.481.18±0.470.3930.016
11.86±0.931.79±0.770.797
31.07±0.911.68±0.670.109
71.82±1.012.18±0.930.172

p<0.05 – statistically significant. aMann-Whitney test; bFriedman analysis

Discussion

Orthodontic force causes gradual compression on the periodontal ligament, which leads to circulatory disorders, such as ischemia and hypoxia in the early stage of orthodontic tooth movement17. Hypoxia and compression caused by orthodontic force stimulate the production of reactive oxygen species and free radicals, which contribute to cellular and tissue damage, especially damaging lipid peroxidation chains18. Vitamin E is a strong biological antioxidant that has several functions: scavenges free radicals, which inhibit lipid peroxidation and inflammation; protects ischemic tissue and hypoxia; provides immunostimulation11,19. Norazlina et al. observed the effect of vitamin E supplementation on bone metabolism in mice treated with nicotine. Their study results suggested that vitamin E can increase trabecular bone formation and prevent bone calcium loss by reducing pro-inflammatory cytokines20.

In the present study, it can be seen that both groups showed increased tooth movement distance as well as increase in the number of osteoclast and osteoblast cells on day 1. This is due to the initial phase of tooth movement after application of orthodontic force21. This phase occurs 24 hours to 48 hours after application of orthodontic force on teeth3.

Our results showed that the number of osteoclasts is higher in group 2 compared to group 1 although the difference was not statistically significant. Miresmaeili et al., in their study on the effect of vitamin C to orthodontic tooth movement, found that osteoclast numbers were significantly higher in the vitamin C group, which hence accelerates tooth movement22. Kale et al., in their research on vitamin D injection, observed a significant amount of Howhip’s lacunae in resorption cavity as a result of osteoclast’s activity23. Future research is required to observe the comparison between Howship’s lacunae and osteoclasts numbers.

In our study, there were statistically significant differences in the mean number of osteoblast cells between both groups at each time observed. Kawakami and Takano-Yamamoto demonstrated an increased osteoclast and osteoblast number with local injection of 1,25-dihydroxyvitamin D3 in the submucosal palatal area of rats subjected to tooth movement on day 7. Increased osteoblast counts were observed on day 1419,24. In another study, Feresin et al. reported that the formation rate and bone volume increased significantly by 65% in rat bone, who were given a vitamin E diet compared to the control group. Their result indicated that a vitamin E diet was able to increase the process of mineralization and bone formation mediated by osteoblast cells25. Diravidamani et al. stated that many drugs that are used to reduce pain had effects on orthodontic tooth movement. Further research should be done to observe vitamin E on pain regulation, because it has anti-inflammatory effect, which is assumed to reduce pain in orthodontic treatment10,2628.

The force mechanism from the separator used in our study was static and the elasticity from the separator is easily lost due to saliva acidity (pH), food and chewing process; a the force of a rubber separator will be reduced by 50–55% within 24 hours29. This is a limitation of our study, as we wanted to analyse for a longer time and with a larger force. The aim of our study was to see the orthodontic tooth movement and not stabilization, so we decided to observe the orthodontic movement within the initial phase, and not all phases until the stabilization phase.

Conclusions

Our findings demonstrated that vitamin E accelerates tooth movement and stimulates bone formation. The number of osteoblast cells in the vitamin E supplemented group is significantly higher than those in the non-vitamin E group. Further studies are needed to evaluate the effect of different doses and types of vitamin E.

Data availability

Underlying data

Open Science Framework: Methods, Figures, and Results from "Effect of Vitamin E Supplementation on Orthodontic Tooth Movement in Wistar Rats, https://doi.org/10.17605/OSF.IO/3S4QB30.

Reporting guidelines

Open Science Framework: ARRIVE checklist for ‘Effect of vitamin E supplementation on orthodontic tooth movement in Wistar rats’, https://doi.org/10.17605/OSF.IO/3S4QB30.

Data are available under the terms of the Creative Commons Attribution 4.0 International license (CC-BY 4.0).

Comments on this article Comments (0)

Version 3
VERSION 3 PUBLISHED 04 Sep 2020
Comment
Author details Author details
Competing interests
Grant information
Copyright
Download
 
Export To
metrics
Views Downloads
F1000Research - -
PubMed Central
Data from PMC are received and updated monthly.
- -
Citations
CITE
how to cite this article
Sufarnap E, Siregar D and Lindawati Y. Effect of vitamin E supplementation on orthodontic tooth movement in Wistar rats [version 1; peer review: 1 approved, 1 not approved]. F1000Research 2020, 9:1093 (https://doi.org/10.12688/f1000research.25709.1)
NOTE: If applicable, it is important to ensure the information in square brackets after the title is included in all citations of this article.
track
receive updates on this article
Track an article to receive email alerts on any updates to this article.

Open Peer Review

Current Reviewer Status: ?
Key to Reviewer Statuses VIEW
ApprovedThe paper is scientifically sound in its current form and only minor, if any, improvements are suggested
Approved with reservations A number of small changes, sometimes more significant revisions are required to address specific details and improve the papers academic merit.
Not approvedFundamental flaws in the paper seriously undermine the findings and conclusions
Version 1
VERSION 1
PUBLISHED 04 Sep 2020
Views
27
Cite
Reviewer Report 25 Sep 2020
Hiroyuki Kanzaki, Maxillo-oral Disorders, Tohoku University Hospital, Sendai, Japan;  Department of Orthodontics, School of Dental Medicine, Tsurumi University, Yokohama, Japan 
Not Approved
VIEWS 27
In this manuscript, the authors examined the effect of vitamin E (VE) supplementation on orthodontic tooth movement (OTM). They found that VE augmented OTM only at day-3. The number of osteoblasts was increased by VE at any time point, though ... Continue reading
CITE
CITE
HOW TO CITE THIS REPORT
Kanzaki H. Reviewer Report For: Effect of vitamin E supplementation on orthodontic tooth movement in Wistar rats [version 1; peer review: 1 approved, 1 not approved]. F1000Research 2020, 9:1093 (https://doi.org/10.5256/f1000research.28373.r71955)
NOTE: it is important to ensure the information in square brackets after the title is included in all citations of this article.
  • Author Response 15 Oct 2020
    Erliera Sufarnap, Department of Orthodontics, Universitas Sumatera Utara, Medan, 20155, Indonesia
    15 Oct 2020
    Author Response
    Dear, Assoc. Prof. Hiroyuki Kanzaki, Maxillo-oral Disorders, Yohoku University Hospital, Sendai, Japan
     
    Thank you for your kind attention and assistance in reviewing our manuscript with the precious advices for ... Continue reading
COMMENTS ON THIS REPORT
  • Author Response 15 Oct 2020
    Erliera Sufarnap, Department of Orthodontics, Universitas Sumatera Utara, Medan, 20155, Indonesia
    15 Oct 2020
    Author Response
    Dear, Assoc. Prof. Hiroyuki Kanzaki, Maxillo-oral Disorders, Yohoku University Hospital, Sendai, Japan
     
    Thank you for your kind attention and assistance in reviewing our manuscript with the precious advices for ... Continue reading
Views
19
Cite
Reviewer Report 09 Sep 2020
Ananto Ali Alhasyimi, Department of Orthodontics, Faculty of Dentistry, Gadjah Mada University (UGM), Yogyakarta, Indonesia 
Approved
VIEWS 19
It’s been an honor for us to review the manuscripts. First of all, please allow me to congratulate the authors for endeavoring to undertake this study which I found very interesting and valuable as a recommendation for further study in ... Continue reading
CITE
CITE
HOW TO CITE THIS REPORT
Alhasyimi AA. Reviewer Report For: Effect of vitamin E supplementation on orthodontic tooth movement in Wistar rats [version 1; peer review: 1 approved, 1 not approved]. F1000Research 2020, 9:1093 (https://doi.org/10.5256/f1000research.28373.r70989)
NOTE: it is important to ensure the information in square brackets after the title is included in all citations of this article.
  • Author Response 15 Oct 2020
    Erliera Sufarnap, Department of Orthodontics, Universitas Sumatera Utara, Medan, 20155, Indonesia
    15 Oct 2020
    Author Response
    Dear Dr Ananto Ali Alhasyimi, Universitas Gadjah Mada, Sleman, Indonesia
    Thank you for your kind assistance in reviewing our manuscript becoming very marvelous manuscript with your advices at many chapters. We have ... Continue reading
COMMENTS ON THIS REPORT
  • Author Response 15 Oct 2020
    Erliera Sufarnap, Department of Orthodontics, Universitas Sumatera Utara, Medan, 20155, Indonesia
    15 Oct 2020
    Author Response
    Dear Dr Ananto Ali Alhasyimi, Universitas Gadjah Mada, Sleman, Indonesia
    Thank you for your kind assistance in reviewing our manuscript becoming very marvelous manuscript with your advices at many chapters. We have ... Continue reading

Comments on this article Comments (0)

Version 3
VERSION 3 PUBLISHED 04 Sep 2020
Comment
Alongside their report, reviewers assign a status to the article:
Approved - the paper is scientifically sound in its current form and only minor, if any, improvements are suggested
Approved with reservations - A number of small changes, sometimes more significant revisions are required to address specific details and improve the papers academic merit.
Not approved - fundamental flaws in the paper seriously undermine the findings and conclusions
Sign In
If you've forgotten your password, please enter your email address below and we'll send you instructions on how to reset your password.

The email address should be the one you originally registered with F1000.

Email address not valid, please try again

You registered with F1000 via Google, so we cannot reset your password.

To sign in, please click here.

If you still need help with your Google account password, please click here.

You registered with F1000 via Facebook, so we cannot reset your password.

To sign in, please click here.

If you still need help with your Facebook account password, please click here.

Code not correct, please try again
Email us for further assistance.
Server error, please try again.