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Hydrogen sulfide regulates bone remodeling and promotes orthodontic tooth movement

机译:硫化氢调节骨质重塑并促进正畸牙齿运动

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摘要

Hydrogen sulfide (H2S) is a gas signaling molecule that has multiple influences on physiological and pathological processes in the mammalian body, including vasodilation, neurotransmission, inflammation, hypoxia sensing and bone remodeling. Our previous studies suggested that H2S might be involved in the periodontal tissue remodeling during the orthodontic tooth movement (OTM) via increasing periodontal ligament cell differentiation, tissue mineralization, bone formation and collagen synthesis. The aim of the present study was to investigate the effects of H2S on alveolar bone remodeling that is associated with tooth movement. Experiments were performed in an OTM mouse model. Sodium hydrosulfide (NaHS), which is a donor of H2S and DL-propargylglycine (PAG) and a cystathionine-gamma-lyase (CSE) inhibitor, which could also decrease H2S expression, were administered intra-peritoneally and respectively. A total of 60 male C57BL6/J mice were divided into 4 groups; Control, NaHS, PAG and combination (PAG+NaHS). The rate of OTM and the bone mineral density (BMD) of alveolar bone were scanned and measured by micro-computed tomography (micro-CT). The number of osteoclasts and expression of the tumor necrosis factor ligand superfamily member-11 (RANKL), alkaline phosphatase (ALP), osteocalcin (OCN) and osteoprotegerin (OPG) in alveolar bone were accessed to evaluate the osteoclastic activity and osteogenesis with histochemistry of tartrate-resistant acid phosphatase staining, immunohistochemistry and reverse transcription-quantitative polymerase chain reaction. In the alveolar bone, NaHS increased the OTM and decreased the BMD, respectively. PAG significantly decrease OTM and increased the BMD. NaHS combined with PAG rescued the PAG-induced changes in the OTM and the BMD. Additionally, the number of osteoclasts, the expression of RANKL, ALP, OCN and the ratio of RANKL/OPG were significantly up-regulated in the NaHS group. In contrast, PAG down-regulated the number of osteoclasts, the expression of RANKL, ALP, OCN and the ratio of RANKL/OPG. These findings suggested that H2S might facilitate the OTM by enhancing alveolar bone remodeling as a result of an increased osteoclastic activity and osteogenesis.
机译:硫化氢(H2S)是一种气体信号传导分子,其对哺乳动物体内的生理和病理过程有多次影响,包括血管舒张,神经递血,炎症,缺氧感应和骨质重塑。我们以前的研究表明,通过增加牙周韧带细胞分化,组织矿化,骨形成和胶原合成,H2S可以参与正畸牙齿运动(OTM)期间的牙周组织重塑。本研究的目的是研究H2S对与牙齿运动相关的肺泡骨重塑的影响。实验在OTM小鼠模型中进行。水硫化钠(NaHS),其是H 2 S和DL-丙基甘氨酸(PAG)的供体和胱硫脲 - γ-裂解剂(CSE)抑制剂,其腹膜内施用,并且分别施用了H2S表达。总共60只雄性C57Bl6 / J小鼠分为4组;控制,NaHs,Pag和组合(PAG + Nah)。通过微计算机断层扫描(Micro-CT)扫描和测量肺泡骨的OTM和骨密度(BMD)的速率。肿瘤坏死因子配体超家族成员-11(RANKL),碱性磷酸酶(ALP),骨钙素(OCN),骨髓素(OPG)和骨盆蛋白(OPG)的骨骨核苷酸骨的数量和肺泡骨中的骨质蛋白酶(OPG)评价与组织化学的骨质体活性和骨质发生酒石酸耐酸性磷酸酶染色,免疫组化和逆转录定量聚合酶链反应。在肺泡骨中,NaHs增加了OTM并分别降低了BMD。 PAG显着降低了OTM并增加了BMD。 Nahs结合PAG救出了OTM和BMD的PAG诱导的变化。另外,在NaHS组中,骨壳体的数量,RANKL,ALP,OCN和RANKL / OPG的比例显着上调。相比之下,PAG下调骨细胞的数量,RANKL,ALP,OCN的表达和RANKL / OPG的比例。这些发现表明H2S可以通过增加的骨质体活性和骨性发生,通过增强肺泡骨重塑来促进OTM。

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