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本文引用的文献

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Anti-Inflammatory Effects of Hypophyllanthin and Niranthin Through Downregulation of NF-κB/MAPKs/PI3K-Akt Signaling Pathways.地构叶素和尼兰汀通过下调 NF-κB/MAPKs/PI3K-Akt 信号通路发挥抗炎作用。
Inflammation. 2018 Jun;41(3):984-995. doi: 10.1007/s10753-018-0752-4.
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Arthritic role of Porphyromonas gingivalis in collagen-induced arthritis mice.牙龈卟啉单胞菌在胶原诱导性关节炎小鼠中的关节炎作用
PLoS One. 2017 Nov 30;12(11):e0188698. doi: 10.1371/journal.pone.0188698. eCollection 2017.
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Stimulates TLR2-PI3K Signaling to Escape Immune Clearance and Induce Bone Resorption Independently of MyD88.刺激TLR2-PI3K信号通路以逃避免疫清除并独立于MyD88诱导骨吸收。
Front Cell Infect Microbiol. 2017 Aug 8;7:359. doi: 10.3389/fcimb.2017.00359. eCollection 2017.
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ERK2 and JNK1 contribute to TNF-α-induced IL-8 expression in synovial fibroblasts.细胞外信号调节激酶2(ERK2)和c-Jun氨基末端激酶1(JNK1)促成肿瘤坏死因子-α(TNF-α)诱导的滑膜成纤维细胞白细胞介素-8(IL-8)表达。
PLoS One. 2017 Aug 14;12(8):e0182923. doi: 10.1371/journal.pone.0182923. eCollection 2017.
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Aggravation of collagen-induced arthritis by orally administered Porphyromonas gingivalis through modulation of the gut microbiota and gut immune system.牙龈卟啉单胞菌经肠道菌群和肠道免疫系统调节口服加重胶原诱导性关节炎。
Sci Rep. 2017 Jul 31;7(1):6955. doi: 10.1038/s41598-017-07196-7.
6
Periodontitis epidemiology: is periodontitis under-recognized, over-diagnosed, or both?牙周炎流行病学:牙周炎是否被低估、过度诊断,还是两者皆有?
Periodontol 2000. 2017 Oct;75(1):45-51. doi: 10.1111/prd.12200.
7
Is macrophage polarization important in rheumatoid arthritis?巨噬细胞极化在类风湿性关节炎中重要吗?
Int Immunopharmacol. 2017 Sep;50:345-352. doi: 10.1016/j.intimp.2017.07.019. Epub 2017 Jul 24.
8
Kava-241 reduced periodontal destruction in a collagen antibody primed Porphyromonas gingivalis model of periodontitis.卡瓦-241 减少了胶原抗体引发的伴放线放线杆菌牙周炎模型中的牙周破坏。
J Clin Periodontol. 2017 Nov;44(11):1123-1132. doi: 10.1111/jcpe.12784. Epub 2017 Sep 21.
9
Matrix Metalloproteinases and Synovial Joint Pathology.基质金属蛋白酶与滑膜关节病理学
Prog Mol Biol Transl Sci. 2017;148:305-325. doi: 10.1016/bs.pmbts.2017.03.003. Epub 2017 May 4.
10
Dysbiosis in chronic periodontitis: Key microbial players and interactions with the human host.慢性牙周炎中的菌群失调:关键微生物及其与宿主的相互作用。
Sci Rep. 2017 Jun 16;7(1):3703. doi: 10.1038/s41598-017-03804-8.

卡瓦-241 对牙龈卟啉单胞菌诱导关节炎小鼠模型关节和全身炎症的抑制作用。

Reduction of Articular and Systemic Inflammation by Kava-241 in a Porphyromonas gingivalis-Induced Arthritis Murine Model.

机构信息

INSERM (French National Institute of Health and Medical Research), UMR 1260, Regenerative Nanomedicine (RNM), FMTS, Strasbourg, France.

Université de Strasbourg, Faculté de Chirurgie Dentaire, Periodontology, Strasbourg, France.

出版信息

Infect Immun. 2018 Aug 22;86(9). doi: 10.1128/IAI.00356-18. Print 2018 Sep.

DOI:10.1128/IAI.00356-18
PMID:29914930
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6105883/
Abstract

Rheumatoid arthritis (RA) is an inflammatory disease that has been linked to several risk factors, including periodontitis. Identification of new anti-inflammatory compounds to treat arthritis is needed. We had previously demonstrated the beneficial effect of Kava-241, a kavain-derived compound, in the management of -induced periodontitis. The present study evaluated systemic and articular effects of Kava-241 in an infective arthritis murine model triggered by bacterial inoculation and primed with a collagen antibody cocktail (CIA) to induce joint inflammation and tissular destruction. Clinical inflammation score and radiological analyses of the paws were performed continuously, while histological assessment was obtained at sacrifice. Mice exposed to and a CIA cocktail and treated concomitantly with Kava-241 exhibited a reduced clinical inflammatory score and a decreased number of inflammatory cells and osteoclasts within joint. Kava-241 treatment also decreased significantly tumor necrosis factor alpha (TNF-α) in serum from mice injected with a Toll-like receptor 2 or 4 (TLR-2/4) ligand, -lipopolysaccharide (LPS). Finally, bone marrow-derived macrophages infected with and exposed to Kava-241 displayed reduced TLR-2/4, reduced mitogen-activated protein kinase (MAPK)-related signal elements, and reduced LPS-induced TNF-α factor (LITAF), all explaining the observed reduction of TNF-α secretion. Taken together, these results emphasized the novel properties of Kava-241 in the management of inflammatory conditions, especially TNF-α-related diseases such as infective RA.

摘要

类风湿关节炎(RA)是一种炎症性疾病,与多种风险因素有关,包括牙周炎。需要寻找新的抗炎化合物来治疗关节炎。我们之前已经证明了卡瓦-241(一种源自卡瓦根的化合物)在治疗诱导的牙周炎方面的有益作用。本研究评估了 Kava-241 在感染性关节炎小鼠模型中的全身和关节作用,该模型由细菌接种引发,并通过胶原抗体鸡尾酒(CIA)预先接种以诱导关节炎症和组织破坏。连续进行爪的临床炎症评分和放射学分析,同时在牺牲时获得组织学评估。暴露于和 CIA 鸡尾酒并同时用 Kava-241 治疗的小鼠表现出较低的临床炎症评分,以及关节内炎症细胞和破骨细胞数量减少。Kava-241 治疗还显著降低了注射 Toll 样受体 2 或 4(TLR-2/4)配体脂多糖(LPS)的小鼠血清中的肿瘤坏死因子-α(TNF-α)。最后,骨髓来源的巨噬细胞感染并暴露于 Kava-241 后,TLR-2/4 减少,丝裂原激活蛋白激酶(MAPK)相关信号元件减少,LPS 诱导的 TNF-α因子(LITAF)减少,所有这些都解释了观察到的 TNF-α分泌减少。总之,这些结果强调了 Kava-241 在管理炎症性疾病方面的新特性,特别是与 TNF-α 相关的疾病,如感染性 RA。