2020
DOI: 10.1002/2211-5463.12937
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Hyperoside ameliorates periodontitis in rats by promoting osteogenic differentiation of BMSCs via activation of the NF‐κB pathway

Abstract: Hyperoside has been reported to possess anti‐inflammatory properties. Here, we confirmed that hyperoside exhibits potential therapeutic properties against periodontitis via promotion of proliferation and osteogenic differentiation of rat bone mesenchymal stem cells through activation of the NF‐κB signaling pathway. Therefore, our study provides evidence that hyperoside may have potential as a novel therapeutic option for periodontitis treatment.

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Cited by 13 publications
(6 citation statements)
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“…Bone marrow stromal cells were isolated from two-week-old male Sprague–Dawley rats obtained from the Experimental Animal Centre, Nanjing Medical University, China, as previously described [ 23 ]. All protocols were carried out in accordance with the guidelines of the Animal Experiment Committee of Nanjing Medical University.…”
Section: Methodsmentioning
confidence: 99%
“…Bone marrow stromal cells were isolated from two-week-old male Sprague–Dawley rats obtained from the Experimental Animal Centre, Nanjing Medical University, China, as previously described [ 23 ]. All protocols were carried out in accordance with the guidelines of the Animal Experiment Committee of Nanjing Medical University.…”
Section: Methodsmentioning
confidence: 99%
“…Subsequently, some crucial external parameters could be evaluated including bone volume and mineral density, trabeculae thickness, and cementoenamel junction (CEJ)-alveolar bone crest (ABC) distance (Liu et al 2010). In ligature-induced periodontitis model, some crucial internal parameters relating to cellular substances could be observed, where histological analyses show osteoclast activity (Ihn et al 2018;Qiao et al 2018) and arrangement of collagen fibers (Adhikari et al 2019;Xu et al 2020).…”
Section: Discussionmentioning
confidence: 99%
“…Alleviated LPS-induced inflammation, oxidative stress, and apoptosis by upregulating SIRT1 to activate Wnt/β-catenin and sonic hedgehog pathways. [ 83 ] 26 Rat peritoneal macrophages 100 μM Inhibited NO production via inhibition of expression of iNOS by attenuation of p44/p42 MAPK, p38 MAPK and JNK [ 84 ] 27 Chondrocytes, Male C57BL/6 mice 10, 20, 40 μM; 20 mg/kg Suppression of PI3K/AKT/NF-κB and MAPK pathways Enhanced Nrf2/HO-1 [ 85 ] 28 HK-2 cells 10, 50, 100 μM Activation of miR-499a-5p/NRIP1 signal pathway [ 86 ] 29 Male SD rats, BMSCs 40 μg/mL Activation of NF-κB pathway to proliferation and osteogenic differentiation [ 87 ] 30 Mouse peritoneal macrophages 5 μM Inhibition of TNF-α, IL-6, NO production, NF-κB activation [ 25 ] 31 Antidepressant effect C6 glioblastoma cells 1 μM Reduced β2-adrenergic sensitivity [ 88 ] 32 C6 glioblastoma cells 1 μM Reduction in β2-AR density in plasma membrane and decrease in corresponding downstream signaling [ 89 ] 33 PC12 cells 2.5, 5, 10 μg/mL Decreased Ca 2+ , upregulation of CREB and BNDF through the cAMP-CREB signal pathway [ 90 ] 34 …”
Section: Pharmacologic Effectmentioning
confidence: 99%