Altın Ahmet, Korkmaz Meltem Zihni, Atak Mehtap, Mercantepe Tolga, Yılmaz Hülya Kılıç
Istanbul Kent University, Faculty of Dentistry, Department of Periodontology, İstanbul, Turkey.
Recep Tayyip Erdogan University, Faculty of Dentistry, Department of Periodontology, Rize, Turkey.
Biomedicine (Taipei). 2023 Dec 1;13(4):44-50. doi: 10.37796/2211-8039.1421. eCollection 2023.
INTRODUCTION: Periodontitis is a common chronic inflammatory disease characterized by the destruction of the supporting structures of the teeth. The host defense mechanisms are responsible for inflamatuar and destructive reactions in periodontitis. Celastrol is one of the most promising components of the plant in Eastern and Southern China that has a long history of use in traditional medicine for the treatment of inflammatory conditions. AIM: The aim of this animal study was to inspect the preventive or restrictive effects of celastrol on periodontitis-related inflammatory host response and alveolar bone loss. METHODS: 24 male Sprague Dawley rats were randomly assigned into 3 groups: control, experimental periodontitis (Ep), and experimental periodontitis-celastrol (Ep-Cel). Periodontitis was induced by placing ligatures sub-paramarginally around the mandibular first molars of the rats in the Ep and Ep-Cel groups and maintaining the ligatures for 15 days. For 14 days following the ligature placement, celastrol administration (1 mg/kg BW day) for the Ep-Cel group and vehicle injection for the control and Ep groups was carried out. At the end of the experiment, mandibula and gingiva samples were obtained after the euthanasia. Alveolar bone loss was measured on serial histological slices; Tumor Necrosis Factor-α and Interleukin-1β levels were measured on gingiva samples by ELISA. RESULTS: Systemic celastrol administration significantly restricted the alveolar bone loss that was higher in rats with periodontitis. (p < 0.05) Tumor Necrosis Factor-α and Interleukin-1β levels that were high in the gingiva of the rats with periodontitis were found significantly lower in rats administered celastrol. (p < 0.05). CONCLUSION: Celastrol restricted periodontitis-related alveolar bone loss by suppressing the inflammatory response.
引言:牙周炎是一种常见的慢性炎症性疾病,其特征是牙齿支持结构遭到破坏。宿主防御机制在牙周炎的炎症和破坏反应中起作用。雷公藤红素是中国东部和南部一种植物中最具前景的成分之一,在传统医学中用于治疗炎症已有悠久历史。 目的:本动物研究的目的是检验雷公藤红素对牙周炎相关炎症宿主反应和牙槽骨丧失的预防或抑制作用。 方法:将24只雄性Sprague Dawley大鼠随机分为3组:对照组、实验性牙周炎组(Ep)和实验性牙周炎-雷公藤红素组(Ep-Cel)。通过在Ep组和Ep-Cel组大鼠下颌第一磨牙的龈下放置结扎丝并维持15天来诱导牙周炎。在放置结扎丝后的14天里,对Ep-Cel组给予雷公藤红素(1毫克/千克体重/天),对对照组和Ep组注射赋形剂。实验结束时,安乐死后获取下颌骨和牙龈样本。在连续的组织切片上测量牙槽骨丧失;通过酶联免疫吸附测定法测量牙龈样本中的肿瘤坏死因子-α和白细胞介素-1β水平。 结果:全身性给予雷公藤红素显著抑制了牙周炎大鼠中较高的牙槽骨丧失。(p < 0.05)在给予雷公藤红素的大鼠中,牙周炎大鼠牙龈中较高的肿瘤坏死因子-α和白细胞介素-1β水平显著降低。(p < 0.05)。 结论:雷公藤红素通过抑制炎症反应抑制了牙周炎相关的牙槽骨丧失。
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