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通过C/EBP和11β-羟基类固醇脱氢酶1型对桦树皮中分离出的桦木醇的调控,牙周炎的抑制作用

Inhibitory Effect of Periodontitis through C/EBP and 11β-Hydroxysteroid Dehydrogenase Type 1 Regulation of Betulin Isolated from the Bark of .

作者信息

Kim Eun-Nam, Jeong Gil-Saeng

机构信息

College of Pharmacy, Chungnam National University, Daejeon 34134, Korea.

出版信息

Pharmaceutics. 2022 Sep 5;14(9):1868. doi: 10.3390/pharmaceutics14091868.

Abstract

Periodontitis is an infectious inflammatory disease of the tissues around the tooth that destroys connective tissue and is characterized by loss of periodontal ligaments and alveolar bone. Currently, surgical methods for the treatment of periodontitis have limitations and new treatment strategies are needed. Therefore, this study evaluated the efficacy of the compound betulin isolated from bark of on the inhibition of periodontitis in vitro and in vivo periodontitis induction models. In the study, betulin inhibited pro-inflammatory mediators, such as tumor necrosis factor, interleukin-6, inducible nitric oxide synthase, and cyclooxygenase-2, in human periodontal ligament cells stimulated with lipopolysaccharide (PG-LPS). In addition, it showed an anti-inflammatory effect by down-regulating 11β-hydroxysteroid dehydrogenase type 1 and transcription factor C/EBP β produced by PG-LPS. Moreover, PG-LPS inhibited the osteogenic induction of human periodontal ligament cells. The protein and mRNA levels of osteogenic markers, such as inhibited osteopontin (OPN) and runt-related transcription factor 2 (RUNX2), were regulated by betulin. In addition, the efficacy of betulin was demonstrated in a typical in vivo model of periodontitis induced by PG-LPS, and the results showed through hematoxylin & eosin staining and micro-computed tomography that the administration of betulin alleviated alveolar bone loss and periodontal inflammation caused by PG-LPS. Therefore, this study proved the efficacy of the compound betulin isolated from in the inhibition of periodontitis and alveolar bone loss, two important strategies for the treatment of periodontitis, suggesting the potential as a new treatment for periodontitis.

摘要

牙周炎是一种发生在牙齿周围组织的感染性炎症疾病,会破坏结缔组织,其特征是牙周韧带和牙槽骨丧失。目前,治疗牙周炎的手术方法存在局限性,需要新的治疗策略。因此,本研究评估了从[具体植物名称]树皮中分离出的化合物桦木醇在体外和体内牙周炎诱导模型中对牙周炎的抑制效果。在该研究中,桦木醇抑制了用牙龈卟啉单胞菌脂多糖(PG-LPS)刺激的人牙周膜细胞中的促炎介质,如肿瘤坏死因子、白细胞介素-6、诱导型一氧化氮合酶和环氧化酶-2。此外,它通过下调PG-LPS产生的11β-羟基类固醇脱氢酶1型和转录因子C/EBPβ发挥抗炎作用。此外,PG-LPS抑制了人牙周膜细胞的成骨诱导。桦木醇调节了成骨标志物如骨桥蛋白(OPN)和 runt相关转录因子2(RUNX2)的蛋白质和mRNA水平。此外,桦木醇的疗效在PG-LPS诱导的典型牙周炎体内模型中得到了证实,苏木精-伊红染色和微型计算机断层扫描结果显示,桦木醇的给药减轻了PG-LPS引起的牙槽骨丧失和牙周炎症。因此,本研究证明了从[具体植物名称]中分离出的化合物桦木醇在抑制牙周炎和牙槽骨丧失方面的疗效,这是治疗牙周炎的两个重要策略,表明其作为牙周炎新治疗方法的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c756/9502078/0768be78b17f/pharmaceutics-14-01868-g001.jpg

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