Abstract
Background
This study was performed to determine the therapeutic effects of diosgenin (DG) which is a steroidal saponin, administered at different doses on alveolar bone loss (ABL) in rats with experimental periodontitis using immunohistochemical and cone-beam computed tomography (CBCT).
Methods
Thirty-two male Wistar rats divided into four equal groups: control (non-ligated), periodontitis (P), DG-48, and DG-96. Sutures were placed at the gingival margin of the lower first molars to induce experimental periodontitis. Then, 48 and 96 mg/kg of DG was administered to the study groups by oral gavage for 29 days. At day 30, the animals were sacrificed and ABL was determined via CBCT. The expression patterns of osteocalcin (OCN), alkaline phosphatase (ALP), type I collagen (Col-1), B cell lymphoma 2 (Bcl 2), Bcl 2-associated X protein (Bax), bone morphogenetic protein 2 (BMP-2), and receptor activator of NF κB ligand (RANKL) were examined immunohistochemically.
Results
Histopathologic examination showed all features of the advanced lesion in the P group. DG use decreased all these pathologic changes. It was observed that periodontitis pathology decreased as the dose increased. DG treatment increased the ALP, OCN, Bcl 2, Col-1, and BMP-2 levels in a dose-dependent manner, compared with the P group (p < 0.05). DG decreased the expression of RANKL and Bax in a dose-dependent manner (p < 0.05). ABL was significantly lower in the DG-48 and DG-96 groups than in the P group (p < 0.05).
Conclusion
Collectively, our findings suggest that DG administration protects rats from periodontal tissue damage with a dose-dependent manner, provides an increase in markers of bone formation, decreases in Bax/Bcl-2 ratio and osteoclast activation.
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Background
Various factors cause the bone loss including systemic diseases, trauma, osteoporosis and periodontal disease [1,2,3]. Bone loss in jaws is critical because especially severe losses leads the loss of function and complicates dental treatment. Therefore, studies have been focused protective and therapeutic treatment of the bone loss [4].
Periodontitis is an inflammatory disease in which the interactions between periodontal bacteria and the host tissue response lead to tissue destruction [4]. Specific groups of oral bacteria populate in dental plaque play a precursor role in the development of periodontal disease, however that once the disease has been stimulated, other factors effect the progression of periodontitis and aggravate the treatment of disease [5]. Increases in oxidative stress, proinflammatory cytokines, and osteoclast cells have major roles in periodontal destruction [2]. Oxidative stress stimulates the transformation of precursor osteoclast cells into mature osteoclasts, leading to pathological changes, followed by the destruction of affected tissue [6,7,8]. Reactive oxygen species (ROS) are highly reactive by-products of oxygen metabolism and they have crucial role in various cellular processes as signalling molecules [9]. ROS causes apoptosis by reducing B-cell lymphoma 2 proteins (Bcl-2) and elevating the expression of Bcl-2-associated X protein (BAX) [10]. In addition, the elevation of ROS levels can damage tissue cells by stimulating proinflammatory cytokine cells and modulating the several pathways such as activation of NFκB ligand (RANKL) pathway, decreasing the protective effect of Nuclear factor red line 2 related factor 2 pathway, c-Jun N-terminal kinase signaling pathway, NOD-like receptor protein 3 [4, 11,12,13]. RANKL is known a member of the tumor necrosis factor superfamily. RANKL is an apoptosis regulator gene and it is a binding partner of osteoprotegerin. RANKL is expressed by several types of cells, including osteoblasts, osteocytes, fibroblasts, and lymphocytes [14]. RANKL induces the activation of osteoclast cells and osteoclastogenesis because it stimulates the formation of osteoclast precursor cells. RANKL-mediated osteoclastogenesis has a critical role in periodontal destruction (Fig. 1) [4, 15, 16].
Growth factors organize cellular activities and improve tissue healing by binding to specific cell receptors. Several studies have used growth factors to enhance periodontal tissue and bone regeneration [17, 18]. BMP-2 belongs to the TGF-β superfamily of proteins and it is a growth factor with roles in tissue regeneration, including the transformation of undifferentiated mesenchymal cells and enhancement of osteoblast differentiation [19]. Furthermore, it stimulates the secretion of several osteoblastic-specific molecules, such as alkaline phosphatase (ALP), osteocalcin (OCN), and type I collagen (Col-1) [15, 20].
Various agents have been used to reduce the effects of ROS on periodontitis, and diosgenin (DG) is one of them. DG is a naturally occurring bioactive steroid saponin. It has been used in several steroidal drugs in the pharmaceutical industry because its chemical structure is similar to the structures of sex hormones [21, 22]. DG exhibits various therapeutic effects, including antioxidative, antidiabetic, anti-inflammatory, and antihyperlipidemic activities [21, 23, 24]. Moreover, DG modulates RANKL and OCN levels, regulates oxidative stress, stimulates signaling in the BMP pathways, and prevents apoptosis [22, 24,25,26,27,28].
To our knowledge, no study has evaluated the effects of different doses DG treatment on periodontal destruction in rats with systemically healthy. Therefore, it is unclear the influence and mechanisms of different doses DG treatment in systemically healthy rats with periodontitis. Here, we hypothesized that DG has antioxidative, anti-inflammatory and anti-resorptive properties and it could prevent periodontal tissue destruction by decreasing RANKL levels, inhibiting periodontal inflammation and cell apoptosis, and inducing bone formation. This study was performed to investigate the therapeutic effects of DG on ALP, OCN, Col-1, BAX, Bcl-2, BMP-2, and RANKL levels, as well as alveolar bone loss (ABL), in rats with experimental periodontitis to ensure basic information for potential DG application and further researches studies.
Methods
Animals
All experimental procedures in the present study were approved by the University Ethics Committee for Animal Experiments, Denizli (PAUHADYEK-2018/33). The Animal Research: Reporting of In Vivo Experiments guidelines were followed in this study. Thirty-two male Wistar albino rats (4 months old, 350–400 g), which were obtained from Pamukkale University Experimental Surgery Application and Research Center, were used in this study. Before initiation of the experimental procedures, the rats were adapted to the experimental environment for ten days; they were housed separately in cages in a room at 21 ± 2 °C and with a 12-h light:12-h dark cycle. All animals had free access to water and food. G* Power 3.1 software was used to calculating of sample size, considering the global significance level of α = 0.05, a sampling power of 95%, and f = 0.86 [24]. Rats were divided into groups by simple randomization using the coin flip method into four groups (n = 8/group): control (non-ligated), periodontitis (P; ligature only), DG-48 (ligature + DG 48 mg/kg/day), and DG-96 (ligature + DG 96 mg/kg/day). The DG (Sigma-Aldrich, Saint Louis, MO, USA) was dissolved in distilled water and administered by oral gavage for 29 days, as in previous studies [22]. Rats in the control and P groups were given 1 ml distilled water by oral gavage during the experiment. All rats were sacrificed at day 30 [15, 29]. Before sacrification, 50 mg/kg body weight of ketamine (Eczacibasi Ilac Sanayi, Istanbul, Turkey) and 5 mg/kg xylazine chloride (Virbaxil®, São Paulo, Brazil) were used for general anesthesia. Hence, all animals were unconscious. The animals were stabilized and their head were placed in the small animal guillotine opening by a specialist animal technician for sacrification. Subsequently, the rats were decapitated rapidly.
Induction of periodontitis model
The experimental procedure was performed under general anesthesia. 50 and 5 mg/kg body weight of ketamine and xylazine chloride respectively were administered intraperitoneally to provide general anesthesia. The cervical areas of the first lower right and left mandibular molars were submarginally ligatured using a 4 − 0 sterile silk suture (Dogsan Ilac Sanayi, Istanbul, Turkey) to stimulate plaque accumulation and periodontal inflammation. The ligatures were checked daily by two operators to prevent the observer bias (AK and ALA).
Three-dimensional imaging
A supine-position cone-beam computed tomography (CBCT) unit (Newtom 5G-XL; QR, Verona, Italy) was used for three-dimensional imaging. The smallest field-of-view of this device (6 cm × 6 cm) was chosen; the exposure settings were 100 mm voxel, 110 kV, 11.4 mA, 9.0 s exposure time, 26.0 s scanning time, enhanced scan, boosted dose, and high-resolution (HiRes) mode. The unit’s proprietary software (NNT, version 12.1; QR) was used for image analysis. All specimens were exposed in the same position with the same exposure parameters. A dentomaxillofacial radiologist with 9 years of experience was blinded to the specimens (MO); this radiologist performed all tomographic procedures and analyzed the images. Figure 2 shows three-dimensional reconstructed and cross-sectional slice images. The distance was measured at cementoenamel junction to the alveolar bone crest and averaged across six areas (the mesial, medial, and distal parts of the buccal–lingual surfaces) of the mandibular first molar teeth for evaluating the linear bone loss (in mm).
Histopathological method
After rats had been sacrificed, mandibular samples were obtained and fixed in 10% neutral-buffered formalin for histopathological evaluation. The samples were decalcified in a solution (Osteofast 1; Biognost, Zagreb, Croatia) for 2 weeks, then routinely processed using automatic tissue processor equipment (Leica ASP300S; Leica Microsystems, Wetzlar, Germany) and immersed in paraffin. Subsequently, a rotary microtome (Leica RM 2155; Leica Microsystems) was used to obtained 5 μm sections from each sample. Each sample was cut along the long axis of the tooth in the mesiodistal direction and stained with hematoxylin and eosin. Histopathological examinations were performed by a single specialist who was blinded to the samples (ÖÖ).
Observations were conducted using a light microscope at ×40 magnification, according to a modified version of histopathological scoring criteria established by Leitao et al. [30]. To standardize the data, five areas from each rat were evaluated and their averages were taken. Neutrophil leukocyte infiltrations were specifically assessed. Inflammatory cell infiltrations, alveolar bone resorption, and degeneration and destruction of the cementum were scored according to previous study [30].
Immunohistochemical method
The streptoavidin-biotin peroxidase technique was performed to the sections selected for immunohistochemical processing. Sections were immunohistochemically stained at 1/100 dilution for all primary antibodies using anti-BMP 2 (ab59348; all from Abcam plc, Cambridge, UK), anti-RANKL (ab216484), anti-ALP (ab224335), Bax (ab53154), anti-Bcl-2 (ab59348), anti-Col-1 (ab34710) and anti-OCN (ab93876) antibody kits according to the manufacturer’s recommendations.
The sections were then embedded with hydrogen peroxide in 3% methanol for 20 min to eliminate activity of endogenous peroxidase. Sections were boiled twice for 5 min with citrate buffer solution and washed in phosphate buffered saline (PBS). The UltraVision Detection System Anti-Polyvalenti HRP Kit (Mouse and Rabbit Specific HRP/DAB Detection Kit-Micro-polymer, ab236466; Abcam plc) was used as the secondary antibody was used as the secondary antibody and 3,3’-diaminobenzidine (DAB) as the chromogen. Sections were incubated with primary antibodies for 60 min at room tempareture. Immunohistochemistry was then performed using biotinylated secondary antibody and streptavidin-alkaline phosphatase conjugate. Sections were incubated with DAB for 3–5 min.
For negative controls, an antibody dilution solution was used instead of primary antibodies. Harris haematoxylin was used for contrast staining and slides were examined under a light microscope. Immunohistochemical findings were scored on a scale of 0 to 3, where 0 = no staining, 1 = mild staining, 2 = moderate staining, and 3 = heavy staining [31]. All immunohistochemical evaluations were performed by a specialized pathologist who was blinded to the samples (ÖÖ). Immunohistochemical analyses were performed using ImageJ 1,48 version (National Institutes of Health, Bethesda MD).
After the classic microscopic analyses, we obtained histomorphometric and immunohistochemical evaluations using an automated image analysis system (Olympus CX41; Olympus Corporation, Tokyo, Japan). The lesioned area was evaluated using proprietary software (cellSens Life Science Imaging Software System; Olympus Corporation).
Statistical analysis
The Shapiro–Wilk test was used to assess whether data exhibited normal distributions. The post hoc Duncan multiple comparison test and one-way analysis of variance were used to analyze the ABL. Independent variables (ALP, BAX, Bcl-2, BMP-2, Col-1, OCN, RANKL, and histopathological scores) were evaluated using the Kruskal–Wallis test. All data are reported as means ± standard deviations for each group (p < 0.05). All analyses were conducted using SPSS software (version 23; IBM Corporation, Armonk, NY, USA).
Results
CBCT findings
Periodontitis was induced in all ligated groups, according to the CBCT findings. The results showed that the control group had no ABL. ABL was significantly lower in the DG-48 and DG-96 groups than in the P group (p < 0.05; Figs. 2 and 3).
Histopathological findings
Histological examination showed that the control group had normal gingival tissue architecture and gingival epithelium; it showed no pathological findings. Hyperemia, ulcers in the gingival epithelial layer, inflammatory reactions in the gingival tissue and periodontal ligament, partial to severe cement destruction, and alveolar bone degradation were observed in the P group. Microscopic evaluations of the DG-48 and DG-96 groups revealed that the treatments ameliorated the pathological findings, compared with the P group. Furthermore, cellular infiltration, ABL, and cement destruction were reduced in the DG-96 group, compared with the DG-48 group (Fig. 4).
Immunohistochemical findings
The expression patterns of ALP, Bcl-2, BAX, Col-1, BMP-2, OCN, and RANKL in mesenchymal cells in all groups were observed immunohistochemically. Positive immunoexpression was indicated by a brown color. During examinations of the ALP, BAX, Bcl-2, BMP-2, Col-1, OCN, and RANKL immunostained sections, slight to negative immunoexpression findings were observed in the control group.
ALP, Bcl-2, BMP-2, Col-1, and OCN expression levels were significantly lower in the P group than in the control group (p < 0.05). Treatment significantly increased the expression levels of ALP, Bcl-2, BMP-2, Col-1, and OCN in the DG groups, compared with the P group (p < 0.05). Additionally, DG-96 was more effective than DG-48 for normalizing immunoexpression (Fig. 5). Statistical analysis results of the immunohistochemical scores are shown in Fig. 3.
BAX and RANKL expression levels increased in the P group, compared with the control group (p < 0.05). Treatment significantly decreased RANKL and BAX levels in the DG groups, compared with the P group (p < 0.05). Finally, DG-96 significantly decreased the expression levels of RANKL and BAX, compared with DG-48 (p < 0.05; Figs. 3 and 5).
Discussion
In the present study, we used histomorphometry, immunohistochemistry, and CBCT to evaluate the effects of DG dose on ABL in experimental periodontitis. To our knowledge, this is the first study regarding the effects of DG in healthy rats with experimental periodontitis. The doses of DG were determined on the basis of previous findings [22, 32, 33].
There are three methods that are frequently used to induce periodontal disease, which are: ligature application, oral bacterial inoculation, and the lipopolysaccharide injection technique. In the ligature model, sterile non-absorbable sutures or orthodontic wires are widely used to induce local irritation and bacterial plaque accumulation. Secondly, mono and mixed cultures of periodontal bacteria are inoculated orally by gavage or topical application. Lastly, lipopolysaccharide extracted from pathogenic bacteria can be directly injected into the gingival sulcus to induce inflammation and stimulate osteoclastogenesis and alveolar bone loss. Among these methods, ligature application induces inflammation and alveolar bone resorption more promptly compared to other methods [34]. Hence, we preferred this method for inducing bone loss.
Micro-computerized tomography is regarded as the “gold standard” method for analyzing trabecular bone and tooth microstructure, evaluating the development of the skull bones, and assessing tissue engineering [35]. However, several studies have evaluated the efficacy of CBCT as an alternative for assessing periodontal defects because micro-computerized tomography involves ultra-high radiation doses and is not routinely used in clinical settings [36]. Thus, Tayman et al. investigated the use of CBCT to measure periodontal defects; they concluded that it provides useful linear and volumetric measurements of such defects in vitro [36]. Other studies have suggested that CBCT can be used to evaluate periodontal defects and the structures and trabecular microarchitecture of alveolar bone [37]. In an experimental study, Lektemur Alpan et al. demonstrated that CBCT measurements of ABL levels were accurate [37]. Thus, we measured ABL using CBCT in this study.
RANKL is the primary regulator of osteoclastogenesis; it has a critical role in osteoclast-associated diseases [38]. Several studies have demonstrated that ABL is associated with high RANKL levels [35, 39]. Zhang et al. performed 24 mg/kg body weight/day, 48 mg/kg body weight/day and 96 mg/kg body weight/day as dosages of DG and they reported that a high dose of DG decreased bone loss by modulating the RANKL and osteoprotegerin levels in an ovariectomized rat model [22]. In an another study, Zhang et al. evaluated protective effects of DG on ABL in ovariectomized rats and they indicated that DG inhibited osteogenesis and osteoclastogenesis by regulating the releasing of important molecules in the Wnt, RANKL or osteoclastogenic cytokine pathways [40]. In previous study, we evaluated the effects of DG on RANKL in diabetic rats with periodontitis and our results showed that 96 mg/kg DG treatment significantly decreased in RANKL levels and ABL. In the present study, DG treatments significantly downregulated the RANKL levels and inhibited RANKL-induced osteoclastogenesis in rats in a dose-dependent manner, compared with the untreated periodontitis group. Furthermore, DG significantly decreased ABL in a dose-dependent manner, compared with the untreated group. These results suggested that DG prevents ABL by inhibiting RANKL expression and RANKL-induced osteoclastogenesis, consistent with the findings of earlier reports [22, 24, 40].
Inflammation can increase oxidative stress, thus, worsening DNA damage and tissue apoptosis [41]. Moreover, periodontal disease reportedly leads to an imbalance between pro- and anti‐apoptotic processes [42]. Therefore, we evaluated apoptotic marker levels in our study. BAX is a member of the Bcl-2 family; expression levels of BAX and Bcl-2 are considered indicators of apoptosis or survival in cells [15, 43]. Wu et al. applied the 10, 50, or 100 mg/kg DG daily in ovariectomized rats and they reported that DG treatment decreases BAX and BAX/Bcl-2 levels and it has a therapeutic potential for ovariectomy-induced cardiac apoptosis [44]. In vitro study demonstrated that 2, 6, and 8 µM doses of DG alleviates the apoptosis by maintaining the Bcl-2 expression [45]. Additionally, 96 mg/kg DG treatment significantly reduced Bax and increased Bcl-2 levels in our previous experimental study [24]. In the present study, we evaluated BAX and Bcl-2 levels to identify the effects of DG on apoptosis signaling pathways. The results showed that experimental periodontitis upregulated and downregulated the expression levels of BAX and Bcl-2, respectively. In contrast, DG treatment upregulated and downregulated the expression levels of Bcl-2 and BAX, respectively, in our experimental periodontitis model. Particularly, DG significantly increased the Bcl-2 levels in higher dose group than low dose group. These results indicate that dose depending DG treatment decreases periodontitis–induced apoptosis by suppressing the expression of BAX and inducing the expression of Bcl-2; these results are also consistent with previous findings [24, 26, 44, 45]. Additionally, apoptosis is a complex process, and additional markers or assays might be needed to confirm this effect comprehensively.
Several biochemical markers have been used to evaluate bone metabolic activity, including ALP, Col-1, OCN, and BMP-2 [10, 37]. ALP is released by osteoblast cells; measurements of ALP level are used to evaluate osteoblastic activity. OCN controls mineral deposition; thus, it has critical roles in bone formation and remodeling [46]. Furthermore, BMP-2 mediates the differentiation of osteoblastic cells and induces the release of ALP, OCN, and Col-1 [15, 19, 20]. Zhao et al. performed 10 mg/kg, 30 mg/kg, and 90 mg/kg DG in retinoic acid-induced osteoporosis in rats and they indicated DG significantly reduced the ALP levels and increased OCN levels in 30 mg/kg, and 90 mg/kg DG groups and promoted bone formation and inhibits bone absorption by regulating bone metabolism and mineralization [27]. Another study applied DG via oral gavage at a dosage of 100 mg/kg body weight daily and they found that DG could enhance the bone formation process through increased Wnt and BMP signaling activity; these pathways regulate the osteogenic differentiation of mesenchymal stem cells and preosteoblasts [25]. Liao et al. found that the arginyl–DG conjugate stimulates BMP-2-induced osteoblastic differentiation with synergistic effects on ALP activity and mineralization [47]. Additionally, Zhang et al. treated the DG group rats by oral gavage with 100 mg/kg body weight DG and they showed that DG has anti-bone loss efficiacy on rat alveolar bone by alleviating the OCN levels [40]. In diabetic rats with experimental periodontitis, we used the 96 mg/kg DG treatment and previous results reported that DG treatment significantly improved the expression of ALP, OCN and BMP-2 in test group [24]. In the present study, DG significantly promoted the expression of ALP, OCN and BMP-2 in test groups than P group. Also, high dose DG treatment significantly promoted BMP-2 and ALP levels compared the low dose group. These findings suggest that DG treatment, especially high dose of DG, enhances bone formation by increasing new bone activity through enhanced expression of ALP, OCN, and BMP-2; this is also consistent with previous findings [24, 25, 27, 40, 47].
Col-1 is an important factor that stimulates osteoblast differentiation and mineral matrix deposition [48]. The increasing of Col-1 supports the ABL formation in the experimental periodontitis [43]. A few studies investigated the association between DG and Col-1 level. In our previous study, 96 mg/kg DG treatment significantly increased the Col-1 levels in diabetic rats with periodontitis [24]. The present study showed periodontitis decreased the Col-1 level and both dose of DG treatment significantly increased the Col-1 level and confirmed the previous study the association between the periodontitis and Col-1 [24, 43]. However, further studies are needed to evaluating DG on Col-1 levels.
This study have several limitation. We did not evaluate the effect of DG on the Wnt pathways or osteoprotegerin levels or other relevant markers of bone metabolism, inflammation and did not compare the CBCT findings with micro-computerized tomography; these were limitations of the present study. Therefore, further studies are needed to investigate the effects of DG on the other bone metabolic pathways and relevant markers expression in periodontal disease. Another limitation of our study is the inability to examine DG in humans by histological examination due to ethical barriers and potential side effects. Ligature induced periodontitis causes acute inflammation in rats however periodontitis is a chronic course in humans in terms of proinflammatory, anti-inflammatory cytokine activities and oxidant/antioxidant balance and that is a limitation. Additionally, we preferred DG doses according to previous studies nonetheless different doses of DG could be evaluated further studies.
Conclusion
The present study indicated that both doses of DG—particularly the higher dose—regulate bone activity, prevent RANKL-induced osteoclastogenesis and improve new bone activity and bone formation. Although limitations, our results indicate that DG administration can prevent alveolar bone damage in periodontal disease.
Data availability
The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.
Abbreviations
- ROS:
-
Reactive oxygen species
- Bcl-2:
-
B-cell lymphoma 2 proteins
- BAX:
-
Bcl-2-associated X protein
- RANKL:
-
NFκB ligand
- BMP-2:
-
Bone morphogenetic protein 2
- ALP:
-
Alkaline phosphatase Osteocalcin (OCN)
- Col-1:
-
Type I collagen
- DG:
-
Diosgenin
- ABL:
-
Alveolar bone loss
- P:
-
Periodontitis
- DG-48:
-
Ligature + DG 48 mg/kg/day
- DG-96:
-
Ligature + DG 96 mg/kg/day
- CBCT:
-
Cone-beam computed tomography
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AK, ALA and TA induced periodontitis, applied experimental procedures. MÖ performed radiographic analyzed and ÖÖ applied the histological examinations. AK and ALA wrote the article. All authors read and approved the final manuscript.
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Kızıldağ, A., Alpan, A.L., Aydın, T.K. et al. Assessment and comparative study of diosgenin doses in alleviating experimental periodontitis. BMC Oral Health 24, 859 (2024). https://doi.org/10.1186/s12903-024-04646-3
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DOI: https://doi.org/10.1186/s12903-024-04646-3