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      Dexmedetomidine inhibits the NF-κB pathway and NLRP3 inflammasome to attenuate papain-induced osteoarthritis in rats

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          Abstract

          Context: Dexmedetomidine (Dex) has been reported to have an anti-inflammatory effect. However, its role on osteoarthritis (OA) has not been explored.

          Objective: This study investigates the effect of Dex on OA rat model induced by papain.

          Materials and methods: The OA Wistar rat model was induced by intraluminal injection of 20 mL of papain mixed solution (4% papain 0.2 mL mixed with 0.03 mol L −1 l-cysteine 0.1 mL) into the right knee joint. Two weeks after papain injection, OA rats were treated by intra-articular injection of Dex (5, 10, or 20 μg kg −1) into the right knee (once a day, continuously for 4 weeks). Articular cartilage tissue was obtained after Dex treatment was completed.

          Results: The gait behavior scores (2.83 ± 0.49), PWMT (15.2 ± 1.78) and PTWL (14.81 ± 0.92) in H-DEX group were higher than that of OA group, while Mankin score (5.5 ± 0.81) was decreased ( p < 0.05). Compared with the OA group, the IL-1β (153.11 ± 16.05 pg mg −1), IL-18 (3.71 ± 0.7 pg mg −1), IL-6 (14.15 ± 1.94 pg/mg) and TNF-α (40.45 ± 10.28 pg mg −1) levels in H-DEX group were decreased ( p < 0.05). MMP-13, NLRP3, and caspase-1 p10 expression in Dex groups were significantly lower than that of OA group ( p < 0.05), while collagen II was increased ( p < 0.05). p65 in the nucleus of Dex groups was significantly down-regulated than that of OA group ( p < 0.05).

          Discussion and Conclusions: Dex can improve pain symptoms and cartilage tissue damage of OA rats, which may be related to its inhibition of the activation of NF-κB and NLRP3 inflammasome.

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          Most cited references43

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          TLR-induced NF-κB activation regulates NLRP3 expression in murine macrophages.

          NLRP3 inflammasome plays a critical role in the activation of caspase-1 and maturation of IL-1β. However, the specific cis- and trans-regulatory elements that determine the extent of NLRP3 expression are not well defined. In this study, we found NLRP3 expression was induced by TLR agonists in murine macrophages in a NF-κB dependent manner. Furthermore, the corresponding NF-κB binding sites (nt -1303 to -1292 and -1238 to -1228) were identified in the NLRP3 promoter. Finally, EMSA and ChIP assays demonstrated LPS-induced NF-κB binding to the NLRP3 promoter. Therefore, out results delineated the molecular mechanisms involved in TLR-induced transcriptional regulation of NLRP3. Copyright © 2012 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
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            Inflammation and angiogenesis in osteoarthritis.

            To quantify the relationship between inflammation and angiogenesis in synovial tissue from patients with osteoarthritis (OA). Hematoxylin and eosin staining and histologic grading for inflammation were performed for 104 patients who met the American College of Rheumatology criteria for OA and had undergone total joint replacement or arthroscopy. A purposive sample of synovial specimens obtained from 70 patients was used for further analysis. Vascular endothelium, endothelial cell (EC) proliferating nuclei, macrophages, and vascular endothelial growth factor (VEGF) were detected by immunohistochemical analysis. Angiogenesis (EC proliferation, EC fractional area), macrophage fractional area, and VEGF immunoreactivity were measured using computer-assisted image analysis. Double immunofluorescence histochemical analysis was used to determine the cellular localization of VEGF. Radiographic scores for joint space narrowing and osteophyte formation in the knee were also assessed. Synovial tissue samples from 32 (31%) of 104 patients with OA showed severe inflammation; thickened intimal lining and associated lymphoid aggregates were often observed. The EC fractional area, EC proliferation, and VEGF immunoreactivity all increased with increasing histologic inflammation grade and increasing macrophage fractional area. In the synovial intimal lining, VEGF immunoreactivity was localized to macrophages and increased with increasing EC fractional area and angiogenesis. No inflammation or angiogenic indices were significantly correlated with radiographic scores. Inflammation and angiogenesis in the synovium are associated with OA. The angiogenic growth factor VEGF generated by the inflamed synovium may promote angiogenesis, thereby contributing to inflammation in OA.
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              NLRP3 as a potentially novel biomarker for the management of osteoarthritis

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                Author and article information

                Journal
                Pharm Biol
                Pharm Biol
                IPHB
                iphb20
                Pharmaceutical Biology
                Taylor & Francis
                1388-0209
                1744-5116
                2019
                23 September 2019
                : 57
                : 1
                : 649-659
                Affiliations
                [a ]Department of Pain Clinic, The Affiliated Lianyungang Oriental Hospital of Xuzhou Medical University , Lianyungang, China;
                [b ]Center for Clinical Research and Translational Medicine, The Affiliated Lianyungang Oriental Hospital of Xuzhou Medical University , Lianyungang, China;
                [c ]Department of Traditional Chinese and Western Medicine, The Affiliated Lianyungang Oriental Hospital of Xuzhou Medical University , Lianyungang, China;
                [d ]Department of Orthopedic, The Affiliated Lianyungang Oriental Hospital of Xuzhou Medical University , Lianyungang, China;
                [e ]Department of Geratology, The Affiliated Lianyungang Oriental Hospital of Xuzhou Medical University , Lianyungang, China
                Author notes
                CONTACT Xue-Ming He xueminghemy@ 123456sina.com Department of Geratology, The Affiliated Lianyungang Oriental Hospital of Xuzhou Medical University , Lianyungang, Jiangsu 222042, China
                Article
                1651874
                10.1080/13880209.2019.1651874
                6764405
                31545916
                00367d9f-f269-4b27-9fca-b34385ff072a
                © 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 15 April 2019
                : 15 July 2019
                : 30 July 2019
                Page count
                Figures: 7, Tables: 0, Pages: 11, Words: 7508
                Funding
                Funded by: Lianyungang Oriental Hospital Foundation
                Award ID: DFYY2017012
                This study was supported by Lianyungang Oriental Hospital Foundation (DFYY2017012).
                Categories
                Research Article

                joint pain,inflammation,paw withdrawal mechanical threshold,paw withdrawal thermal latency,articular cartilage

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