Department of Periodontology, Faculty of Dentistry, Pamukkale University, Denizli, Turkey.
Department of Periodontology, Faculty of Dentistry, Atatürk University, Erzurum, Turkey.
BMC Oral Health. 2024 Jul 28;24(1):859. doi: 10.1186/s12903-024-04646-3.
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).
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.
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).
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.
本研究旨在通过免疫组织化学和锥形束 CT(CBCT)评估不同剂量薯蓣皂苷元(DG)治疗实验性牙周炎大鼠牙槽骨丧失(ABL)的疗效。
32 只雄性 Wistar 大鼠分为 4 组:对照组(未结扎)、牙周炎组(P)、DG-48 组和 DG-96 组。在下颌第一磨牙牙龈边缘放置缝线以诱导实验性牙周炎。然后,通过口服灌胃给予研究组 48 和 96mg/kg 的 DG,共 29 天。第 30 天,处死动物,通过 CBCT 测量 ABL。通过免疫组织化学检测骨钙素(OCN)、碱性磷酸酶(ALP)、I 型胶原(Col-1)、B 细胞淋巴瘤 2(Bcl 2)、Bcl 2 相关 X 蛋白(Bax)、骨形态发生蛋白 2(BMP-2)和核因子 κB 受体激活剂配体(RANKL)的表达模式。
组织病理学检查显示 P 组所有的病变特征均为晚期病变。DG 减少了所有这些病理变化。观察到随着剂量的增加,牙周病病理学减少。与 P 组相比,DG 治疗以剂量依赖性方式增加了 ALP、OCN、Bcl 2、Col-1 和 BMP-2 水平(p<0.05)。DG 以剂量依赖性方式降低 RANKL 和 Bax 的表达(p<0.05)。DG-48 和 DG-96 组的 ABL 明显低于 P 组(p<0.05)。
总之,我们的研究结果表明,DG 给药以剂量依赖性方式保护大鼠免受牙周组织损伤,增加骨形成标志物,降低 Bax/Bcl-2 比值和破骨细胞激活。