Yuanyuan Liu, Xiumei Guan, Min Cheng, Xin Li, Yueyang Pan, Zhiliang Guo
Dept. of Stomatology, School of Stomatology, Affiliated Hospital of Weifang Medical University, Weifang 261053, China.
School of Clinical Medicine, Weifang Medical University, Weifang 261053, China.
Hua Xi Kou Qiang Yi Xue Za Zhi. 2017 Oct 1;35(5):473-478. doi: 10.7518/hxkq.2017.05.005.
The aim of this study is to identify the role of adenosine triphosphate-sensitive potassium channel (KATP) in hydrogen sulfide (H₂S)-induced inhibition of high glucose (HG)-induced osteoblast damage.
Osteoblasts from rat mandible were cultured and identified. The osteoblasts were then treated with HG, H₂S, KATP channel opener pinacidil (Pia), and KATP channel blocker glibenclamide (Gli). Western blot method was performed to detect the expression of KATP channel protein. CCK8, reverse transcriptase polymerase chain reaction (RT-PCR) , and image analysis were used to determine the effects of H₂S-KATP on the proliferation, differentiation, and mineralization of osteoblasts.
The expression of KATP channel protein in osteoblasts was significantly decreased under the influence of HG. H₂S pretreatment significantly inhibited HG on KATP channel protein down-regulation. Moreover, H₂S pretreatment significantly inhibited the effect of HG on the proliferation of osteoblasts, thereby preventing HG-induced inhibition of osteoblasts differentiation and mineralization. Meanwhile, the KATP channel blocker effectively blocked the H₂S on osteoblasts and had a protective effect.
Through the KATP channel, H₂S inhibited osteoblasts damage induced by HG.
本研究旨在确定三磷酸腺苷敏感性钾通道(KATP)在硫化氢(H₂S)诱导的对高糖(HG)诱导的成骨细胞损伤的抑制作用中的作用。
培养并鉴定来自大鼠下颌骨的成骨细胞。然后用HG、H₂S、KATP通道开放剂吡那地尔(Pia)和KATP通道阻滞剂格列本脲(Gli)处理成骨细胞。采用蛋白质免疫印迹法检测KATP通道蛋白的表达。使用CCK8、逆转录聚合酶链反应(RT-PCR)和图像分析来确定H₂S-KATP对成骨细胞增殖、分化和矿化的影响。
在HG的影响下,成骨细胞中KATP通道蛋白的表达显著降低。H₂S预处理显著抑制HG对KATP通道蛋白的下调作用。此外,H₂S预处理显著抑制HG对成骨细胞增殖的影响,从而防止HG诱导的成骨细胞分化和矿化抑制。同时,KATP通道阻滞剂有效阻断了H₂S对成骨细胞的作用并具有保护作用。
H₂S通过KATP通道抑制HG诱导的成骨细胞损伤。