|Year : 2012 | Volume
| Issue : 1 | Page : 2-10
Biological response at the cellular level within the periodontal ligament on application of orthodontic force - An update
Nazeer Ahmed Meeran
Departments of Orthodontics and Dentofacial Orthopedics, Priyadarshini Dental College and Hospital, Tamil Nadu, India
|Date of Web Publication||10-Apr-2012|
Nazeer Ahmed Meeran
Old No 6, New No 11, NGO Colony First Street, Nanganallur, (Kendriya Vidyalaya School Road), Chennai - 600 114, Tamil Nadu
Source of Support: None, Conflict of Interest: None
Orthodontic force elicits a biological response in the tissues surrounding the teeth, resulting in remodeling of the periodontal ligament and the alveolar bone. The force-induced tissue strain result in reorganization of both cellular and extracellular matrix, besides producing changes in the local vascularity. This in turn leads to the synthesis and release of various neurotransmitters, arachidonic acid, growth factors, metabolites, cytokines, colony-stimulating factors, and enzymes like cathepsin K, matrix metalloproteinases, and aspartate aminotransferase. Despite the availability of many studies in the orthodontic and related scientific literature, a concise integration of all data is still lacking. Such a consolidation of the rapidly accumulating scientific information should help in understanding the biological processes that underlie the phenomenon of tooth movement in response to mechanical loading. Therefore, the aim of this review was to describe the biological processes taking place at the molecular level on application of orthodontic force and to provide an update of the current literature.
Keywords: Interleukins, orthodontic force, periodontal ligament, prostaglandins
|How to cite this article:|
Meeran NA. Biological response at the cellular level within the periodontal ligament on application of orthodontic force - An update. J Orthodont Sci 2012;1:2-10
|How to cite this URL:|
Meeran NA. Biological response at the cellular level within the periodontal ligament on application of orthodontic force - An update. J Orthodont Sci [serial online] 2012 [cited 2019 Feb 19];1:2-10. Available from: http://www.jorthodsci.org/text.asp?2012/1/1/2/94769
| Introduction|| |
Teeth can be moved through the alveolar bone when appropriate orthodontic force is applied to them. This is mainly due to the fact that mechanical loading of a biological system results in strain, which subsequently leads to biological responses at the cellular and molecular level, aiming at adaptation of the system to the changed conditions.  As a result of this principle, remodeling of the periodontal ligament (PDL) and the alveolar bone takes place around teeth on application of orthodontic force.  Recent research in the biological basis of tooth movement has provided detailed insight into cellular, molecular, and tissue-level reactions to orthodontic forces. , There are many theories proposed regarding orthodontic tooth movement. ,,, The pressure-tension theory proposed by Schwartz in 1932 is the simplest theory describing tooth movement on mechanical loading.  On the pressure side, the biological events are as follows: disturbance of blood flow in the compressed PDL, cell death in the compressed area of the PDL (hyalinization), resorption of the hyalinized tissue by macrophages, and undermining bone resorption by osteoclasts beside the hyalinized tissue, which ultimately results in tooth movement. On the tension side, blood flow is activated where the PDL is stretched, which promote osteoblastic activity and osteoid deposition, which later mineralizes. ,
The fluid flow hypothesis, describing a mechanism by which osteocytes respond to mechanical forces, states that locally evoked strain derived from the displacement of fluid in the canaliculi is very important.  When loading occurs, interstitial fluid is squeezed through the thin layer of the non-mineralized matrix surrounding the cell bodies and cell processes, resulting in local strain at the cell membrane and activation of the affected osteocytes. 
According to piezoelectric theory, there is production of piezoelectric signal on application of orthodontic force, which quickly reduces to zero. On removal of the mechanical force, the piezoelectric signal is again produced, but in the opposite direction. The possible sources of this electric current could be collagen, hydroxyapatite, or the mucopolysaccharide fraction of the ground substance.  On application of orthodontic force, the alveolar bone adjacent to the tooth bends and the area of concavity accumulates negative charges, resulting in bone deposition. Areas of convexity are associated with positive charges, resulting in bone resorption. These currents are affected by the nature of the fluid present within the canaliculi. The small voltages thus generated are called "Streaming Potentials." 
Recently,  it has been proposed that the pressure-tension theory is not simple and might involve more complicated biological tissue response, suggesting that bone apposition could be induced by (1) the load exerted by stretched fibers of the PDL, which may also induce a slight bending of the alveolar wall; (2) direct resorption by unloading of the alveolar wall in the case of low forces; and (3) indirect resorption as repair due to ischemia following the application of high forces.  Schwarz proposed the classic concept of the optimal force.  He defined optimal continuous force as ''the force leading to a change in tissue pressure that approximated the capillary vessels' blood pressure, thus preventing their occlusion in the compressed periodontal ligament.'' According to Schwarz,  forces well below the optimal level cause no reaction in the PDL. Forces exceeding the optimal level would lead to areas of tissue necrosis, thereby preventing frontal bone resorption. Tooth movement would thus be delayed until undermining resorption eliminates the necrotic tissue obstacle.
| Inflammatory Mediators in The Periodontal Ligament|| |
Prostaglandins (PGs) are a group of chemical messengers and are derivatives of arachidonic acid.  They are synthesized within seconds following physical injury to the cells and tissues.  Prostaglandin E2 (PGE2) is a potent vasodilator and can increase the vascular permeability. It also has chemotactic properties and can stimulate the formation of osteoclasts, resulting in a subsequent increase in bone resorption. PGs are produced through two different pathways by the action of the enzyme cyclooxygenase on arachidonic acid: the constitutive isoform or cyclooxygenase-1 (COX-1) and the inducible isoform or cyclooxygenase-2 (COX-2). The PGs resulting after either pathway activation are different. 
The COX family of enzymes consists of two proteins that convert arachidonic acid, a 20-carbon polyunsaturated fatty acid comprising a portion of the plasma membrane phospholipids of most cells, to PGs.  The constitutive isoform (COX-1) is found in almost all tissues and is tissue protective. In contrast, COX-2, the inducible isoform of COX, appears to be limited in basal conditions within most tissues, and de novo synthesis is activated by cytokines, bacterial lipopolysaccharides, or growth factors to produce PGs in large amounts during inflammatory processes occurring due to cell injury. 
It has been found that PGs have an important role in promoting bone resorption. Although the exact role of PGs in bone resorption is not clear, it is thought to do so by stimulating cells to produce cyclic adenosine monophosphate, which is an important chemical messenger for bone resorption. ,
Research proved that the application of orthodontic force increased the synthesis of PGs, which in turn stimulated osteoclastic bone resorption.  A similar study on cats by Davidovitch et al,  also showed increased levels of PGE2 in the alveolar bone, as a result of application of orthodontic force. The histological data were supported by the finding of Chumbley et al,  that Indomethacin, an inhibitor of PG synthesis, also inhibited orthodontic tooth movement.
Leiker et al studied the long-term effects of varying concentrations and frequencies of injectable, exogenous PGE2 on the rate of tooth movement in rats and reported that injections of exogenous PGE2 over an extended period of time in rats did enhance the amount of tooth movement. However, there was an increase in the amount of root resorption with increasing numbers and concentrations of the PGE2 injections, which could be a potential concern.
Sekhavat et al,  reported that Misoprostol was effective in enhancing tooth movement in doses as low as 10-25 μg/kg, twice daily. It was also noticed that Misoprostol did not significantly increase the amount of root resorption. They suggested that oral Misoprostol could be used to enhance orthodontic tooth with minimal root resorption. However, long-term studies are needed to justify the use of PGs to accelerate orthodontic tooth movement in clinical practice.
Orthodontic forces result in capillary vasodilatation in the PDL, resulting in migration of inflammatory cells as well as cytokine production by these cells. This in turn helps in the process of bone remodeling.  Cytokines are proteins acting as signals between the cells of the immune system, produced during the activation of immune cells and usually act locally although some act systemically with overlapping functions. Cytokines like interleukin-1 (IL-1), interleukin-6 (IL-6), interleukin-8 (IL-8), and tumor necrosis factor-α (TNF-α) have been proved to be associated with bone remodeling. 
IL-1 predominantly exists in two forms, α and β, of which IL-1β is the form mainly involved in bone metabolism, stimulation of bone resorption, and inhibition of bone formation. IL-1β also plays a central role in the inflammatory process, and large amounts of IL-1β are present in inflamed gingival tissues. They are released within 12 to 24 h after orthodontic force application and play an important role in initiating bone resorption and tooth movement. 
It was found that both macrophages and neutrophils predominate in IL-1β production in inflamed gingival tissues.  The staining of feline PDL cells for IL-1β showed the presence of bound signal complexes in the plasma membrane, which was expected, as it is known that receptors for IL-1β are present on fibroblasts. 
IL-6 is produced by both lymphoid and non-lymphoid cells and can induce osteoclastic bone resorption through an effect on osteo-clastogenesis. , IL-6 has been identified in human gingival tissues and cells; and participates in the molecular events associated with inflammatory periodontal diseases  and tissue destruction in periodontitis. 
The levels of IL-6 increase significantly 24 h after mechanical loading and play an important role in initiating tooth movement. After the application of force, the induction of both IL-1β and IL-6 was observed to reach a maximum on day 3 and to decline thereafter. 
TNF-α is a pro-inflammatory cytokine that is often over-expressed in periodontitis and is responsible for alveolar bone resorption during periodontal breakdown. ,, The possibility that TNF-α is involved in normal physiological processes is supported by its function in osteoclastogenesis. Receptor activator of nuclear factor kappa-B ligand (RANKL) and its receptor receptor activator of nuclear factor k B (RANK), which are present on osteoblasts and precursor osteoclasts, respectively, have been identified as the key factors that stimulate osteoclast formation. 
Recent studies analyzing the cytokine expression pattern in compression and tension sides of the PDL during orthodontic tooth movement in humans, by means of real-time polymerase chain reaction, found that both the pressure and tension sides showed higher expression of all the cytokines when compared to the PDL of normal teeth which served as control. The compression side exhibited higher expression of TNF-α, RANKL, and matrix metalloproteinase I (MMP-1), whereas the tension side presented higher expression of IL-10, tissue inhibitor of MMP-I(TIMP-1), type I collagen, osteoprotegerin (OPG), and osteocalcin. The expression of transforming growth factor-β was similar in both pressure and tension sides.  These findings strongly suggest that TNF-α plays a pivotal role in the bone resorption process, thus helping in orthodontic tooth movement. ,,,,
It is now clear that RANKL, together with macrophage-colony stimulating factor, is required for osteoclast formation from precursor monocytes and macrophages.  The natural inhibitor of RANK-RANKL interactions is the soluble TNF receptor-like molecule OPG, which binds to RANKL and prevents its ligation, thereby preventing osteoclast differentiation and activation. The RANKL protein was found to be predominant in inflammatory cells around inflamed tissues adjacent to areas of pathological bone loss in periodontal disease , and is associated with the progress of periodontal disease. They have a major role in orthodontic tooth movement.
| Tissue Response to Mechanical Forces|| |
The PDL lies between the cementum and alveolar bone, acting as a cushion to withstand mechanical forces applied to teeth.  It receives the applied mechanical forces and responds to these external forces by remodeling. It is likely that PDL cells stimulated by forces of mastication, occlusal contact, and orthodontic treatment produce local factors that participate not only in the maintenance and remodeling of the ligament itself, but also in the metabolism of adjacent alveolar bone.
The most dramatic remodelling changes incident to orthodontic tooth movement occur in the PDL. Application of a continuous force on the crown of the tooth leads to tooth movement within the alveolus that is marked initially by narrowing of the periodontal membrane, particularly in the marginal area. If the duration of movement is divided into an initial and a secondary period, direct bone resorption is found notably in the secondary period, when the hyalinized tissue has disappeared after undermining bone resorption. During the crucial stage of initial application of force, the tissue reveals a glass like appearance in light microscopy, termed hyalinization. It represents a sterile necrotic area, generally limited to 1 or 2 mm in diameter. The process displays three main stages: degeneration, elimination of destroyed tissue, and establishment of a new tooth attachment. 
A clear relationship between force level, timing, and extent of hyalinization could not be found despite the availability of abundant research. , Even with a force as low as 5 cN, hyalinization occurred and the timing of the event seemed to be independent of the force level.  The assumption that higher forces lead to more hyalinization could not be confirmed. An interesting finding from a recent study, however, was that an initially light and gradually increasing force resulted in less hyalinization than a heavier initial force that increased to the same end force level.  It is prudent to use lighter forces for initiating orthodontic tooth movement and then gradually increasing the force levels, instead of using heavy force right at the start.
In the secondary period of tooth movement, the PDL is considerably widened. The osteoclasts attack the bone surface over a much wider area and, provided the force is kept within certain limits, further bone resorption will be predominantly of the direct type. The fibrous attachment apparatus is somewhat reorganized by the production of new periodontal fibrils. These are attached to the root surface and parts of the alveolar bone wall where direct resorption is not occurring by the deposition of new tissue, in which the fibrils become embedded. 
The main feature is the deposition of new bone on the alveolar surface from which the tooth is moving away. Cell proliferation is usually seen after 30 to 40 h in young human beings. Shortly after cell proliferation has started, osteoid tissue is deposited on the tension side. The original periodontal fibres become embedded in the new layers of osteoid, which mineralizes in the deeper parts. New bone is deposited until the width of the membrane has returned to normal limits, and simultaneously fibrous system is remodelled. Concomitantly with bone apposition on the periodontal surface on the tension side, an accompanying resorption process occurs on the spongiosa surface of the alveolar bone. This tends to maintain the dimension of the supporting bone tissue. ,
In vitro studies have proved that the expression and production of some inflammatory mediators (PGE2, IL-1β) are promoted by mechanical stimulation of the PDL. , PGs of the E series play an important role in the pathogenesis of chronic periodontitis by regulating production of osteoclast activating factor in activated lymphocytes.  PGE2 have an important role in orthodontic tooth movement, which has been conclusively proven in the literature.
The induction of both IL-1β and IL-6 was observed to reach a maximum on day 3 after mechanical loading and declines thereafter. This shows that they have an important role in initiating bone resorption and subsequent tooth movement during orthodontic treatment. It must be acknowledged that any interference in the signaling pathway resulting in reduced production of PGE2, IL-1β, and IL-6 would significantly delay tooth movement, which might be the reason for differences in the rate of initial tooth movement in different patients. The same could be the reason for the initial delay in orthodontic tooth movement seen in adults when compared to adolescent patients. 
PDL cells, under mechanical stress, may induce secretion of osteoclasts through up-regulation of RANKL expression via PGE2 synthesis during orthodontic tooth movement. It has been shown that compressive force up-regulated RANKL expression and induction of COX-2 in human PDL cells in vitro.  It is a well-known fact that there is a local increase in PGs in the PDL and alveolar bone during orthodontic treatment.  Several studies have shown an arrest in tooth movement in experimental animals when non-steroidal anti-inflammatory drugs were administered. , Macrophages have the ability to produce cytokines, such as IL-1β and IL-6, the levels of which are known to increase during orthodontic tooth movement.  Non-steroidal anti-inflammatory drugs must be avoided in orthodontic patients, as they would delay tooth movement and prolong the treatment duration.
The number and distribution patterns of RANKL- and RANK-expressing osteoclasts change when excessive orthodontic force is applied to periodontal tissue, and IL-1β and TNF-α are expressed in osteoclasts in inflamed rat periodontal tissues. The presence of RANKL in periodontal tissues, during experimental tooth movement of rat molars, shows that RANKL is regulated by inflammatory cytokines in the PDL in response to mechanical stress.  The RANKL levels increase 24 h after mechanical loading and play an important role in initiating orthodontic tooth movement. Compressive forces are more important for an increase in RANKL levels compared to tensile forces. This indicates that the biomechanics used to initiate tooth movement could play a role in the increase in RANKL levels and subsequent rate of tooth movement.
Kanzaki et al. showed that the local RANKL gene transfer into the periodontal tissue significantly enhanced RANKL expression and secretion of osteoclast in periodontal tissue without any systemic effects. The rate of tooth movement was significantly increased in the RANKL gene transfer side. It was conclusively proved that the transfer of RANKL gene to the periodontal-tissue, activated osteoclast secretion and accelerated the amount of experimental tooth movement. They proposed that local RANKL gene transfer might be a useful tool not only for shortening the duration of orthodontic treatment, but also for moving ankylosed teeth.
Long-term studies are needed to validate the effectiveness of the local RANKL gene transfer as an useful tool to reduce the treatment time, by accelerating the rate of tooth movement in orthodontic patients undergoing fixed appliance treatment. The potential use of the local RANKL gene transfer in moving ankylosed teeth has to be further evaluated to justify its use.
| Pulp Tissue Response to Mechanical Forces|| |
Dental pulp is the soft connective tissue that supports the dentine. It consist of the odontoblastic zone, cell free zone of Weil, cell-rich zone, and the pulp core, which can be seen in a histological slide preparation. The principal cells of the pulp are odontoblast, fibroblast, undifferentiated ectomesenchymal cells, macrophages, and dendritic cells. The innervation is from the sensory afferent from trigeminal nerve and sympathetic branches from superior cervical ganglion. Pulp consists of both myelinated and unmyelinated nerves. An extensive plexus of nerves in the cell-free zone is seen called the subodontoid plexus of Rushkov.
Orthodontic forces not only tend to produce mechanical damage and inflammatory reactions in the periodontium  but also cause cell damage, inflammatory changes, and circulatory disturbances in dental pulp.  Calcitonin gene-related peptide (CGRP) and substance P present in the dental pulp have been associated with the mediation of pulpal inflammation.  CGRP is a major sensory neuropeptide which has been found to evoke the release of IL-6 and IL-8 from synovial fibroblasts in patients with rheumatoid arthritis.  Substance P is another sensory neuropeptide released from the peripheral endings of sensory nerves during inflammation, capable of modifying the secretion of pro-inflammation cytokines from immunocompetent cells, and has also been reported to induce the secretion of IL-1β, IL-6, and TNF-α from monocytes. , The fact that the expression of CGRP and substance P is increased in dental pulp in response to bucally directed orthodontic tooth movement of the upper first molar in rats positively reinforces the fact that these neuropeptides might be involved in inflammation of the dental pulp at the time of orthodontic tooth movement. 
| Gingival Crevicular Fluid During Orthodontic Tooth Movement|| |
Gingival crevicular fluid (GCF) is an inflammatory exudate present in the gingival sulcus. The aqueous component of GCF is primarily derived from the serum; however, the gingival tissue through which the fluid passes, along with bacteria present in the tissue and gingival crevice, can modify its composition.  Therefore, its constituents, which are derived from a variety of sources, including microbial dental plaque, host inflammatory cells, host tissue, and serum, vary according to the condition of the periodontal tissues and the predominant bacterial flora present. In general, cells, immunoglobulins, lysosomal enzymes, microorganisms, and toxins can be detected in GCF, while the mechanism of bone resorption might also be related to the release of inflammatory mediators present in GCF.
Recently, a number of GCF constituents have been shown to be diagnostic markers of active tissue destruction in periodontal diseases  although only a few studies have focused on those involved in bone remodeling during orthodontic tooth movement.
During the course of orthodontic treatment, the forces exerted produce a distortion of the PDL extracellular matrix, resulting in alterations in cellular shape and cytoskeletal configuration. Such events lead to the synthesis and presence in the deeper periodontal tissues of extracellular matrix components, tissue-degrading enzymes, acids, and inflammatory mediators; induce cellular proliferation and differentiation; and promote wound healing and tissue remodeling. These produce an alteration in the GCF flow rate and its components. 
Glycosaminoglycans (GAG) have been detected in GCF samples from sites around teeth affected by such conditions as chronic gingivitis, chronic periodontitis, and juvenile periodontitis. , GCF collected from around the canine tooth subjected to orthodontic force showed an increase in the GAG components particularly hyaluronic acid and chondroitin sulfate.  The cytokine levels in the GCF peaked 24 h after application of orthodontic forces.
The GCF concentrations of IL-1β and IL-6 were found to be significantly higher in a group with severe periodontal disease compared with controls.  It was demonstrated that the GCF IL-1β and TNF-α levels had a positive correlation to mean pocket depths, which led to the suggestion that those cytokines may be involved in the pathogenesis of periodontal diseases.  The GCF isolated from tooth, 24 h after being subjected to orthodontic forces, showed an increase in the levels of IL-1β, IL-6, TNF-α, epidermal growth factor and β2 -microglobulin, when compared to controls.  IL-8 was found to be associated with the bone remodeling process in orthodontic patients.  The level of pro-inflammatory cytokines such as IL-1β, IL-6, and TNF-α reached a significant level at 24 h after application of orthodontic forces. IL-8 reached a significant elevation after 1 month.  It was also found that force induced IL-8 secretion from the PDL cells required the presence of IL-1β in sufficient quantity. 
The lysosomal cysteine protease cathepsin B is known to play an important role in the resolution of organic matrix, a final step in bone resorption. During human orthodontic tooth movement, mechanically stimulated Cathepsin B levels were analyzed with the help of fluorospectrometry and western blot analysis. The Cathepsin B levels were found to be significantly increased when compared to the control teeth, which may be involved in extracellular matrix degradation in response to mechanical stress.  Immunocytochemical studies demonstrated that cathepsin B and cathepsin L were localized in the PDL of the rat molar and were expressed in compressed sites during experimental tooth movement. There was a three-fold increase in cathepsin B and four-fold increase in cathepsin L when compared to the control.  This proves that Cathepsin B and Cathepsin L play an important role in initial orthodontic tooth movement by initiating bone resorption.
The expression of cathepsin K, a novel collagenolytic enzyme specifically expressed in osteoclasts, was investigated in the rat maxillary teeth during experimental tooth movement by in situ hybridization histochemistry with a non-radioisotopic complementary ribonucleic acid (cRNA) probe for rat cathepsin K. Cathepsin K messenger ribonucleic acid (mRNA) expression was detected in the mono- and multi-nuclear osteoclasts on the pressure side of the alveolar bone at 12 h after force application, and the distribution and number of cathepsin K mRNA-positive osteoclasts increased time-dependently on the pressure side. At 3-4 days, there was a marked increase in cathepsin K mRNA-positive osteoclasts on both pressure and tension side of the alveolar bone in response to tooth movement. At 7-12 days, the cathepsin K mRNA-positive osteoclasts on both sides had disappeared. These suggest that the recruitment of osteoclasts on the pressure side begins during the initial stage of orthodontic tooth movement and the site-specific early induction of cathepsin K mRNA may cause an imbalance in the relative resorption activities on the pressure and tension side incident to such movement.  The role of cathepsin K in orthodontic tooth movement and its mechanism of action could be made further clear by controlled experimental studies.
MMPs are enzymes that play a central role in PDL remodeling, both in physiological and in pathological conditions. Collagenase-1 (MMP-1) and collagenase-2 (MMP-8), because they share a unique ability to cleave native triple-helical interstitial collagens, can initiate this tissue remodeling. MMP-8 degranulation by polymorphonuclear leukocytes is among the pivotal factors in pathological collagen destruction during periodontal diseases. Study done by Apajalahti  showed that MMP-2 levels significantly increased in the GCF 4-8 h after force application, while MMP-1 level failed to show any significant increase. Ingman  too found similar results when conducting the study by the immunofluorometric assay over a period of 1 month. There was a 12-fold increase in the orthodontic GCF when compared to the control GCF. The MMP-8 levels in orthodontic GCF were lower than those detected in gingivitis and periodontitis GCF, but significantly higher than in control GCF. This proves that MMPs, particularly MMP-2, play an important role in orthodontic tooth movement and tissue remodeling.
Cantarellaa  found that compression force induced a significant increase of MMP-1 protein after 1 h; the increase lasted until the third hour of force application and disappeared thereafter. The tension force induced significantly increased levels of the MMP-1 protein after just 1 h of force application. MMP-2 protein was induced by compression and increased significantly in a time-dependent fashion, reaching a peak after 8 h of force application. On the tension side, MMP-2 was significantly increased after 1 h, but gradually returned to basal levels within 8 h. Immunolocalization of collagenase-3 (MMP-13) done by Leonardi  showed that there was an increase in MMP-13 very early following the application of an orthodontic force in both PDL and alveolar bone. This indicates that MMP-13 also plays an important role during orthodontic tooth movement.
Analysis of the GCF in patients with periodontal disease  revealed that there was an increase in RANKL and a decrease in the OPG levels; and subsequently the ratio of RANKL concentration to that of OPG in GCF samples was significantly higher for periodontal disease patients than for healthy subjects. This shows that both RANKL and OPG contribute to osteoclastic bone destruction in periodontal disease. Experimental compressive forces on the PDL resulted in a 16.7-fold increase in RANKL secretion and a 2.9-fold decrease in OPG secretion when compared to the control. , This confirms that the RANKL/RANK/OPG system plays an important role in orthodontic tooth movement.
Alkaline phosphatase activity in the GCF is known to decrease during active tooth movement. This decrease was found to be significant during the first month of active tooth movement and started to stabilize later. , Batra  found that the alkaline phosphatase activity in the GCF showed an increase during canine retraction which peaked during the 14th day of retraction followed by a significant fall in activity in the 21st day. It is one of the important enzymes required in initiating orthodontic tooth movement and sustaining it for a 2 week period. Any defect in the production of this enzyme could interfere and delay orthodontic tooth movement.
Aspartate aminotransferase (AST) is a soluble enzyme that is normally confined to the cytoplasm of cells, but is released to the extra-cellular environment upon cell death. The activity levels of AST in the GCF are considered to be important in regulating alveolar bone resorption during orthodontic tooth movement.
Ever since the presence of AST enzyme in GCF has been demonstrated,  several studies have observed that the levels of AST activity in GCF may reflect the magnitude of periodontal tissue destruction in periodontitis. , However, there are only few studies which have investigated a possible role of AST activity levels in tissue remodeling incidental to orthodontic forces. AST activity in the GCF was found to be highest in the first week of orthodontic force application and there was a gradual reduction in the activity during the next 3 weeks.  Thus, it has the potential to serve as a biological marker to monitor orthodontic tooth movement. Similarly, lactate dehydrogenase activity in the GCF can be used as a diagnostic tool for monitoring orthodontic tooth movement in clinical practice. ,,
Leptin, , a polypeptide hormone, has been classified as a cytokine and is mainly secreted from the adipose tissue in humans. Leptin and its receptor share structural and functional similarities with members of the long-chain helical cytokines: IL-6, IL-11, IL-12, leukemia inhibitory factor, granulocyte-colony-stimulating factor, and oncostatin M.
It has been suggested that leptin orchestrates the host response to inflammatory and infectious stimuli; as it stimulates the immune system by enhancing cytokine production and phagocytosis by macrophages.  Thus, the overall increase in leptin during inflammation and infection indicates that leptin is part of the immune response and host defense mechanisms. Previous studies have suggested a relationship between periodontal disease and leptin levels. Since the presence of leptin within healthy and marginally inflamed gingiva has been demonstrated,  several studies have observed that the levels of GCF leptin activity may play an important role in the development of periodontal disease. Karthikeyan  reported that leptin levels decreased progressively in GCF as periodontal disease progressed.
Recently, it has been suggested that leptin plays a significant role in bone formation by virtue of its direct effect on osteoblast proliferation and differentiation, and in prolonging the life span of human primary osteoblasts by inhibiting apoptosis.  Leptin is also involved in anti-osteogenic effects by acting centrally on the hypothalamus.  Thus, leptin at high local concentrations protects the host from inflammation and infection. They also play an important role in maintaining marginal bone levels.
It was recently found that the concentration of leptin in GCF is decreased by orthodontic tooth movement and this conclusively proved that leptin may have been one of the mediators responsible for orthodontic tooth movement. 
IL-17 has been found to be increased in patients with periodontitis, while it was barely detectable in sera from periodontally healthy individuals.  The role of IL-17 in orthodontic tooth movement and its potential to serve as a marker for validating the tooth movement remains a potential area for future research.
| Conclusion|| |
The orthodontic displacement of a tooth is the result of a mechanical stimulus, generated by a force applied to the crown of a tooth, which results in an acute inflammatory response in periodontal tissues, which in turn may trigger the cascade of biological events associated with bone remodeling.  This leads to the synthesis and release of various neurotransmitters, arachidonic acid, growth factors, metabolites, cytokines, colony-stimulating factors, and enzymes like cathepsin K, MMPs, and AST, which are ultimately responsible for initiating bone remodeling and subsequent tooth movement. Any interference with the release of these neurotransmitters and enzymes could delay or hamper orthodontic tooth movement. With the increased scope of gene therapy, the possibility that the rate of tooth movement could be increased by local gene transfer is very much real and could go a long way in reducing the treatment duration of orthodontic patients. However, well-designed experimental studies are needed for the same in order to evaluate their clinical efficiency and validate their use, as this is an era of evidence-based dentistry.
| References|| |
|1.||Reitan K. Tissue behavior during orthodontic tooth movement. Am J Orthod 1960;46:881-900. |
|2.||Masella RS, Meister M. Current concepts in biology of orthodontic tooth movement. Am J Orthod 2006;129:458-68. |
|3.||Sekhavat AR, Mousavizadeh K, Pakshir HR, Aslani FS. Effect of misoprostol, a prostaglandin E1 analog on orthodontic tooth movement in rats. Am J Orthod Dentofacial Orthop 2002;122:542-7. |
|4.||Karras JC, Miller JR, Hodges JS, Beyer JP, Larson BE. Effect of alendronate on orthodontic tooth movement in rats. Am J Orthod Dentofacial Orthop 2009;136:843-7. |
|5.||Baumrind S. A reconsideration of the propriety of the "pressure-tension" hypothesis. Am J Orthod 1969;55:12-22. |
|6.||Heller IJ, Nanda R. Effect of metabolic alteration of periodontal fibers on orthodontic tooth movement. An experimental study. Am J Orthod 1979;75:239-58. |
|7.||Schwartz AM. Tissue changes incidental to orthodontic tooth movement. Int J Orthodontia 1932;18:331-52. |
|8.||Reitan K. The initial tissue reaction incident to orthodontic tooth movement as related to the influence of function; an experimental histologic study on animal and human material. Acta Odontol Scand Suppl 1951;6:1-240. |
|9.||von Böhl M, Kuijpers-Jagtman AM. Hyalinization during orthodontic tooth movement: A systematic review on tissue reactions. Eur J Orthod 2009;31:30-6. |
|10.||Melsen B. Biological reaction of alveolar bone to orthodontic tooth movement. Angle Orthod 1999;69:151-8. |
|11.||Goulet GC, Cooper DM, Coombe D, Zernicke RF. Influence of cortical canal architecture on lacunocanalicular pore pressure and fluid flow. Comput Methods Biomech Biomed Engin 2008;11:379-87. |
|12.||Weinbaum S, Cowin SC, Zeng Y. A model for the excitation of osteocytes by mechanical loading-induced bone fluid shear stresses. J Biomech 1994;27:339-60. |
|13.||Sandy JR, Farndale RW, Meikle MC. Recent advances in understanding mechanically induced bone remodeling and their relevance to orthodontic theory and practice. Am J Orthod Dentofacial Orthop 1993;75:212-22. |
|14.||Melsen B. Tissue reaction to orthodontic tooth movement- A new paradigm. Eur J Orthod 2001;23:671-81. |
|15.||Schwarz AM. Tissue changes incident to orthodontic tooth movement. Int J Orthod 1932;18:331-52. |
|16.||Funk CD. Prostaglandins and leukotrienes: Advances in eicosanoid biology. Science 2001;294:1871-5. |
|17.||Mitchell JA, Larkin S, Williams TJ. Cyclooxygenase-2: Regulation and relevance in inflammation. Biochem Pharmacol 1995;50:1535-42. |
|18.||Feng L, Xia Y, Garcia GE, Hwang D, Wilson CB. Involvement of reactive oxygen intermediates in cyclooxygenase-2expression induced by interleukin-1, tumor necrosis factor-alpha and lipopolysaccharide. J Clin Invest 1995;95:1669-75. |
|19.||Klein DC, Raisz LG. Prostaglandins: Stimulation of bone resorption in tissue culture. Endocrinology 1970;86:1436-40. |
|20.||Raisz LG, Sandberg AL, Goodson JM, Simmons HA, Mergenhagen SE. Complement-dependent stimulation of prostaglandin synthesis and bone resorption. Science 1974;185:789-91. |
|21.||Yamasaki K, Miura F, Suda T. Prostaglandin as a mediator of bone resorption induced by experimental tooth movement in rats. J Dent Res 1980;59:1635-42. |
|22.||Davidovitch Z, Nicolay OF, Ngan PW, Shanfeld JL. Neurotransmitters, cytokines, and the control of alveolar bone remodeling in orthodontics. Dent Clin North Am 1988;32:411-35. |
|23.||Chumbley AB, Tuncay OC. The effects of Indomethacin on the rate of tooth movement in cats. Am J Orthod 1986;89:312-4. |
|24.||Leiker BJ, Nanda RS, Currier GF, Howes RI, Sinha PK. The effects of exogenous prostaglandins on orthodontic tooth movement in rats. Am J Orthod Dentofacial Orthop 1995;108:380-8. |
|25.||Sekhavat AR, Mousavizadeh K, Pakshir HR, Aslani FS. Effect of misoprostol, a prostaglandin E1 analog, on orthodontic tooth movement in rats. Am J Orthod Dentofacial Orthop 2002;122:542-7. |
|26.||Davidovitch Z, Nicolay OF, Ngan PW, Shanfeld JL. Neurotransmitters, cytokines, and the control of alveolar bone remodeling in orthodontics. Dent Clin North Am 1988;32:411-35. |
|27.||Kwan Tat S, Padrines M, Théoleyre S, Heymann D, Fortun Y. IL-6, RANKL, TNF-alpha/IL-1: Interrelations in bone resorption pathophysiology. Cytokine Growth Factor Rev 2004;15:49-60. |
|28.||Saito M, Saito S, Ngan PW, Shanfeld J, Davidovitch Z. Interleukin 1 beta and prostaglandin E are involved in the response of periodontal cells to mechanical stress in vivo and in vitro. Am J Orthod 1991;99:226-40. |
|29.||Lo YJ, Liu CM, Wong MY, Hou LT, Chang WK. Interleukin 1beta-secreting cells in inflamed gingival tissue of adult periodontitis patients. Cytokine 1999;11:626-33. |
|30.||Dinarello CA, Savage N. Interleukin-1 and its receptor. Crit Rev Immunol 1989;9:1-20. |
|31.||Ishimi Y, Miyaura C, Jin CH, Akatsu T, Abe E, Nakamura Y, et al. IL-6 is produced by osteoblasts and induces bone resorption. J Immunol 1990;50:3297-303. |
|32.||Kurihara N, Bertolini D, Suda T, Akiyama Y, Roodman GD. IL-6 stimulates osteoclast-like multinucleated cell formation in long term human marrow cultures by inducing IL-1 release. J Immunol 1990;144:4226-30. |
|33.||Bartold PM, Haynes DR. Interleukin-6 production by human gingival fibroblasts. J Periodontal Res 1991;26:339-45. |
|34.||Irwin CR, Myrillas TT. The role of IL-6 in the pathogenesis of periodontal disease. Oral Dis 1998;4:43-7. |
|35.||Alhashimi N, Frithiof L, Brudvik P, Bakhiet M. Orthodontic tooth movement and de novo synthesis of proinflammatory cytokines. Am J Orthod Dentofacial Orthop 2001;119:307-12. |
|36.||Roberts FA, McCaffery KA, Michalek SM. Profile of cytokine mRNA expression in chronic adult periodontitis. J Dent Res 1997;76:1833-9. |
|37.||Rossomando EF, Kennedy JE, Hadjimichael J. Tumour necrosis factor alpha in gingival crevicular fluid as a possible indicator of periodontal disease in humans. Arch Oral Biol 1990;35:431-4. |
|38.||Stashenko P, Jandinski JJ, Fujiyoshi P, Rynar J, Socransky SS. Tissue levels of bone resorptive cytokines in periodontal disease. J Periodontol 1991;62:504-9. |
|39.||Lacey DL, Timms E, Tan HL, Kelley MJ, Dunstan CR, Burgess T, et al. Osteoprotegerin ligand is a cytokine that regulates osteoclast differentiation and activation. Cell 1998;93:165-76. |
|40.||Garlet TP, Coelho U, Silva JS, Garlet GP. Cytokine expression pattern in compression and tension sides of the periodontal ligament during orthodontic tooth movement in humans. Eur J Oral Sci 2007; 115:355-62. |
|41.||Haynes DR, Atkins GJ, Loric M, Crotti TN, Geary SM, Findlay DM. Bidirectional signaling between stromal and hemopoietic cells regulates interleukin-1 expression during human osteoclast formation. Bone 1999;25:269-78. |
|42.||Crotti TN, Smith MD, Findlay DM, Zreiqat H, Ahern MJ, Weedon H, et al. Factors regulating osteoclast formation in human tissues adjacent to peri-implant bone loss: Expression of receptor activator NFkappaB, RANK ligand and osteoprotegerin. Biomaterials 2004;25:565-73. |
|43.||Ogasawara T, Yoshimine Y, Kiyoshima T, Kobayashi I, Matsuo K, Akamine A, et al. In-situ expression of RANKL, RANK, osteoprotegerin and cytokines in osteoclasts of rat periodontal tissue. J Periodontal Res 2004;39:42-9. |
|44.||Nyman S, Gottlow J, Karring T, Lindhe J. The regenerative potential of the periodontal ligament. An experimental study in the monkey. J Clin Periodontol 1982;9:257-65. |
|45.||Ren Y, Maltha JC, Kuijpers-Jagtman AM. Optimum force magnitude for orthodontic tooth movement: A systematic literature review. Angle Orthod 2003;73:86-92. |
|46.||Kohno T, Matsumoto Y, Kanno Z, Warita H, Soma K. Experimental tooth movement under light orthodontic forces: Rates of tooth movement and changes of the periodontium. J Orthod 2002;29:129-36. |
|47.||Kurol J, Owman-Moll P. Hyalinization and root resorption during early orthodontic tooth movement in adolescents. Angle Orthodnone 1998;68:161-5. |
|48.||Tomizuka R, Shimizu Y, Kanetaka H, Suzuki A, Urayama S, Kikuchi M, et al. Histological evaluation of the effects of initially light and gradually increasing force on orthodontic tooth movement. Angle Orthod 2007;77:410-6. |
|49.||Shimizu N, Yamaguchi M, Goseki T, Ozawa Y, Saito K, Takiguchi H, et al. Cyclic-tension force stimulates interleukin-1 beta production by human periodontal ligament cells. J Periodontal Res 1994;29:328-33. |
|50.||Yamaguchi M, Shimizu N, Goseki T, Shibata Y, Takiguchi H, Iwasawa T, et al. Effect of different magnitudes of tension force on prostaglandin E2 production by human periodontal ligament cells. Arch Oral Biol 1994;39: 877-84. |
|51.||Yoneda T, Mundy GR. Prostaglandins are necessary for osteoclast-activating factor production by activated peripheral blood leucocytes. J Exp Med 1979;149:279-83. |
|52.||Nishijima Y, Yamaguchi M, Kojima T, Aihara N, Nakajima R, Kasai K. Levels of RANKL and OPG in gingival crevicular fluid during orthodontic tooth movement and effect of compression force on releases from periodontal ligament cells in vitro. Orthod Craniofac Resnone 2006;9:63-70. |
|53.||Mostafa YA, Weaks-Dybvig M, Osdoby P. Orchestration of tooth movement. Am J Orthod 1983;83:245-50. |
|54.||Sandy JR, Harris M. Prostaglandins and tooth movement. European J Orthod; 1984;6:175-82. |
|55.||Yamasaki K, Shibata Y, Fukuhara T. The effect of prostaglandins on experimental tooth movement in monkeys. J Dent Res 1982;61:1444-6. |
|56.||Walker JB, Buring SM. NSAID impairment of orthodontic tooth movement. Ann Pharmacother 2001;35:113-5. |
|57.||Saito M, Saito S, Ngan PW, Shanfeld J, Davidovitch Z. Interleukin 1 beta and prostaglandin E are involved in the response of periodontal cells to mechanical stress in vivo and in vitro. Am J Orthod Dentofacial Orthop 1991;99:226-40. |
|58.||Kanzaki H, Chiba M, Arai K, Takahashi I, Haruyama N, Nishimura M, et al. Local RANKL gene transfer to the periodontal tissue accelerates orthodontic tooth movement. Gene Thernone 2006;13:678-85. |
|59.||Rygh P, Bowling K, Hovlandsdal L, Williams S. Activation of the vascular system: A main mediator of periodontal fiber remodeling in orthodontic tooth movement. Am J Orthod 1986;89:453-68. |
|60.||Mostafa YA, Iskander KG, El-Mangoury NH. Iatrogenic pulpal reactions to orthodontic extrusion. Am J Orthod Dentofacial Orthop 1991;99:30-4. |
|61.||Silverman JD, Kruger L. An interpretation of dental innervation based upon the pattern of calcitonin gene-related peptide (CGRP)-immuno reactive thin sensory axons. Somatosens Res 1987;5:157-75. |
|62.||Raap T, Jüsten HP, Miller LE, Cutolo M, Schölmerich J, Straub RH. Neurotransmitter modulation of interleukin6 (IL-6) and IL-8 secretion of synovial fibroblasts inpatients with rheumatoid arthritis compared to osteoarthritis. J Rheumatol 2000;27:2558-65. |
|63.||Rameshwar P, Ganea D, Gascón P. In vitro stimulatory effect of substance P on hematopoiesis. Blood 1993;81:391-8. |
|64.||Lotz M, Vaughan JH, Carson DA. Effect of neuropeptides on production of inflammatory cytokines by human monocytes. Science 1998;241:1218-21. |
|65.||Norevall LI, Matsson L, Forsgren S. Main sensory neuropeptides, but not VIP and NPY, are involved in bone remodeling during orthodontic tooth movement in the rat. Ann N Y Acad Sci 1998;865:353-9. |
|66.||Tollefsen T, Saltvedt E. Comparative analysis of gingival fluid and plasma by crossed immunoelectroforeseis. J Periodont Res 1980;15:96-106. |
|67.||Lamster IB, Novak MJ. Host mediators in gingival crevicular fluid: Implications for the pathogenesis of periodontal disease. Crit Rev Oral Biol Med 1992;3:31-60. |
|68.||Kavadia-Tsatala S, Kaklamanos EG, Tsalikis L. Effects of orthodontic treatment on gingival crevicular fluid flow rate and composition: Clinical implications and applications. Int J Adult Orthodon Orthognath Surg 2002;17:191-205. |
|69.||Last KS, Stanbury JB, Embery G. Glycosaminoglycans in human gingival crevicular fluid as indicators of active periodontal disease. Arch Oral Biol 1985;30:27581. |
|70.||Embery G, Oliver WM, Stanbury JB, Purvis JA. The electrophoretic detection of acidic glycosaminoglycans in human gingival sulcus fluid. Arch Oral Biol 1982;27:177-9. |
|71.||Ren Y, Vissink A. Cytokines in crevicular fluid and orthodontic tooth movement. Eur J Oral Sci 2008;116:89-97. |
|72.||Mogi M, Otogoto J, Ota N, Inagaki H, Minami M, Kojima K. Interleukin 1 beta, interleukin 6, beta 2-microglobulin, and transforming growth factor-alpha in gingival crevicular fluid from human periodontal disease. Arch Oral Biol 1999;44:535-9. |
|73.||Yavuzyilmaz E, Yamalik N, Bulut S, Ozen S, Ersoy F, Saatçi U. The gingival crevicular fluid interleukin-1 beta and tumor necrosis factor-alpha levels in patients with rapidly progressive periodontitis. Aust Dent J 1995;40:46-9. |
|74.||Uematsu S, Mogi M, Deguchi T. Interleukin IL-1, IL-6, Tumor necrosis factor-α, epidermal growth factor, and 2-microglobulin levels are elevated in gingival crevicular fluid during human orthodontic tooth movement. J Dent Res 1996;75:562-7. |
|75.||Tuncer BB, Ozmeriç N, Tuncer C, Teoman I, Cakilci B, Yücel A, et al. Levels of IL-8 during tooth movement. Angle Orthod 2005;75:631-6. |
|76.||Ren Y, Hazemeijer H, de Haan B, Qu N, de Vos P. Cytokine profiles in crevicular fluid during Orthodontic tooth movement of Short and long durations. J Periodontol 2007;78:453-8. |
|77.||Maeda A, Soejima K, Bandow K, Kuroe K, Kakimoto K, Miyawaki S, et al. Force-induced IL-8 from periodontal ligament cells requires IL-1 α. J Dent Res 2007;86:629-34. |
|78.||Sugiyama Y, Yamaguchi M, Kanekawa M, Yoshii M, Nozoe T, Nogimura A, et al. The level of cathepsin B in GCF during human orthodontic tooth movement. Eur J Orthod 2003;25:71-6. |
|79.||Yamaguchi M, Ozawa Y, Nogimura A, Aihara N, Kojima T, Hirayama Y, et al. Cathepsins B and L increased during response of periodontal ligament cells to mechanical stress in vitro. Connect Tissue Res 2004;45:181-9. |
|80.||Ohba Y, Ohba T, Terai K, Moriyama K. Expression of cathepsin K mRNA during experimental tooth movement in rat as revealed by in situ hybridization. Arch Oral Biol 2000;45:65-9. |
|81.||Apajalahti S, Sorsa T, Railavo S, Ingman T. The in vivo levels of matrix metalloproteinase-1 and -8 in gingival crevicular fluid during initial orthodontic tooth movement. J Dent Res 2003;82:1018-22. |
|82.||Ingman T, Apajalahti S, Mäntylä P, Savolainen P, Sorsa T. Matrix metalloproteinase 1 and 8 in GCF during orthodontic tooth movement: A pilot study during 1 month follow- up after fixed appliance activation. Eur J Orthod 2005;27:202-7. |
|83.||Cantarella G, Cantarella R, Caltabiano M, Risuglia N, Bernardini R, Leonardi R. Levels of matrix metalloproteinases 1 and 2 in human gingival crevicular fluid during initial tooth movement. Am J Orthod Dentofacial Orthop 2006;130:568.e11-6. |
|84.||Leonardi R, Talic NF, Loreto C. MMP-13 (collagenase 3) immunolocalisation during initial orthodontic tooth movement in rats. Acta Histochem 2006;109: 215-20. |
|85.||Mogi M, Otogoto J, Ota N, Togari A. Differential expression of RANKL and osteoprotegerin in gingival crevicular fluid of patients with periodontitis. J Dent Res 2004;83:166-9. |
|86.||Nishijima Y, Yamaguchi M, Kojima T, Aihara N, Nakajima R, Kasai K. Levels of RANKL and OPG in gingival crevicular fluid during orthodontic tooth movement and effect of compression force on releases from periodontal ligament cells in vitro. Orthod Craniofac Res 2006;9:63-70. |
|87.||Yamaguchi M. RANK/RANKL/OPG during orthodontic tooth movement. Orthod Craniofac Res 2009;12:113-9. |
|88.||Asma AA. Crevicular alkaline phosphatase activity during orthodontic tooth movement: Canine retraction stage. J Med Sci 2008;8:228-33. |
|89.||Batra P, Kharbanda O, Duggal R, Singh N, Parkash H. Alkaline phosphatase activity in gingival crevicular fluid during canine retraction. Orthod Craniofac Res 2006;9:44-51. |
|90.||Chambers DA, Crawford JM, Mukherjee S, Cohen RL. Aspartate aminotransferase increases in crevicular fluid during experimental periodontitis in beagle dogs. J Periodontol 1984;55:526-30. |
|91.||McCulloch CA. Host enzymes in gingival crevicular fluid as diagnostic indicators of periodontitis. J Clin Periodontol 1994;21:497-506. |
|92.||Persson GR, DeRouen TA, Page RC. Relationship between gingival crevicular fluid levels of aspartate aminotransferase and active tissue destruction in treated chronic periodontitis patients. J Periodontal Res 1990;25:81-7. |
|93.||Rohaya MAW, Shahrul Hisham ZA, Khazlina K. Preliminary study of aspartate aminotransferase activity in gingival crevicular fluids during orthodontic tooth movement. J Appl Sci 2009;9:1393-6. |
|94.||Serra E, Perinetti G, D'Attilio M, Cordella C, Paolantonio M, Festa F, et al. Lactate dehydrogenase activity in gingival crevicular fluid during orthodontic treatment. Am J orthod 2003;124:206-11. |
|95.||Perinetti G, Serra E, Paolantonio M, Bruè C, Meo SD, Filippi MR, et al. Lactate dehydrogenase activity in human gingival crevicular fluid during orthodontic treatment: A controlled, short-term longitudinal study. J Periodontol 2005;76:411-7. |
|96.||Fantuzzi G, Faggioni R. Leptin in the regulation of immunity, inflammation, and hematopoiesis. J Leukoc Biol 2000;68:437-46. |
|97.||Johnson RB, Serio FG. Leptin within healthy and diseased human gingiva. J Periodontol 2001;72:1254-7. |
|98.||Zhang Y, Proenca R, Maffei M, Barone M, Leopold L, Friedman JM. Positional cloning of the mouse obese gene and its human homologue. Nature 1994;372:425-32. |
|99.||Karthikeyan BV, Pradeep AR. Leptin levels in gingival crevicular fluid in periodontal health and disease. J Periodontal Res 2007;42:300-4. |
|100.||Bozkurt FY. Gingival crevicular fluid leptin levels in periodontitis patients with long-term and heavy smoking. J Periodontol 2006;77:634-40. |
|101.||W³odarski K, W³odarski P. Leptin as a modulator of osteogenesis. Ortop Traumatol Rehabil 2009;11:1-6. |
|102.||Dilsiz A, Kiliç N, Aydin T, Ates FN, Zihni M, Bulut C. Leptin levels in gingival crevicular fluid during orthodontic tooth movement. Angle Orthod 2010;80:504-8. |
|103.||Schenkein HA, Koertge TE, Brooks CN, Sabatini R, Purkall DE, Tew JG. IL-17 in sera from patients with aggressive periodontitis. J Dent Res 2010;89:943-7. |
|This article has been cited by|
||Mechanical stress induced S100A7 expression in human dental pulp cells to augment osteoclast differentiation
| ||Hataichanok Charoenpong,Thanaphum Osathanon,Prasit Pavasant,Nuttapol Limjeerajarus,Boonrit Keawprachum,Chalida N. Limjeerajarus,Vipaporn Cheewinthamrongrod,Tanapat Palaga,Veera Lertchirakarn,Patcharee Ritprajak |
| ||Oral Diseases. 2019; |
|[Pubmed] | [DOI]|
||Does Oxidative Stress Induced by Alcohol Consumption Affect Orthodontic Treatment Outcome?
| ||Jorge M. Barcia,Sandra Portolés,Laura Portolés,Alba C. Urdaneta,Verónica Ausina,Gema M. A. Pérez-Pastor,Francisco J. Romero,Vincent M. Villar |
| ||Frontiers in Physiology. 2017; 8 |
|[Pubmed] | [DOI]|
||Dental pulp cells promote the expression of receptor activator of nuclear factor-?B ligand, prostaglandin E2 and substance P in mechanically stressed periodontal ligament cells
| ||Taiki Morikawa,Kenichi Matsuzaka,Kei Nakajima,Toshihiko Yasumura,Kenji Sueishi,Takashi Inoue |
| ||Archives of Oral Biology. 2016; 70: 158 |
|[Pubmed] | [DOI]|
||Review of common conditions associated with periodontal ligament widening
| ||Hamed Mortazavi,Maryam Baharvand |
| ||Imaging Science in Dentistry. 2016; 46(4): 229 |
|[Pubmed] | [DOI]|