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Broadleaf Mahonia attenuates granulomatous lobular mastitis-associated inflammation by inhibiting CCL-5 expression in macrophages

机译:阔叶红花病通过抑制巨噬细胞中的CCL-5表达来减轻肉芽肿性小叶性乳腺炎相关的炎症

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摘要

Granulomatous lobular mastitis (GLM) is a type of chronic mammary inflammation with unclear etiology. Currently systematic corticosteroids and methitrexate are considered as the main drugs for GLM treatment, but a high toxicity and risk of recurrence greatly limit their application. It is therefore an urgent requirement that safe and efficient natural drugs are found to improve the GLM prognosis. Broadleaf Mahonia (BM) is a traditional Chinese herb that is believed to have anti-inflammatory properties according to ancient records of traditional Chinese medicine. The present study investigated this belief and demonstrated that BM significantly inhibited the expression of interleukin-1β (IL-1β), IL-6, cyclooxygenase-2 and inducible nitric oxide synthase in RAW264.7 cells, but had little influence on the cell viability, cell cycle and apoptosis. Meanwhile, the lipopolysaccharide-induced elevation of reactive oxygen species and nitric oxide was also blocked following BM treatment, accompanied with decreased activity of nuclear factor-κB and MAPK signaling. A cytokine array further validated that BM exhibited significant inhibitory effects on several chemoattractants, including chemokine (C-C motif) ligand (CCL)-2, CCL-3, CCL-5 and secreted tumor necrosis factor receptor 1, among which CCL-5 exhibited the highest inhibition ratio in cell and clinical GLM specimens. Collectively, the results show that BM is a novel effective anti-inflammatory herb in vitro and ex vivo, and that CCL-5 may be closely associated with GLM pathogenesis.
机译:肉芽肿性小叶性乳腺炎(GLM)是一种慢性乳腺炎,病因尚不清楚。目前,系统性的皮质类固醇和甲氨蝶呤被认为是GLM治疗的主要药物,但是高毒性和复发风险极大地限制了它们的应用。因此,迫切需要找到安全有效的天然药物来改善GLM的预后。阔叶红Mah(BM)是一种传统中草药,根据古代中医记载,它被认为具有抗炎特性。本研究对此信念进行了研究,并证明了BM可以显着抑制RAW264.7细胞中白介素-1β(IL-1β),IL-6,环氧合酶-2和诱导型一氧化氮合酶的表达,但对细胞活力的影响很小,细胞周期与凋亡。同时,BM处理后,脂多糖诱导的活性氧和一氧化氮的升高也被阻止,同时核因子-κB活性和MAPK信号传导降低。细胞因子阵列进一步验证了BM对几种趋化因子具有明显的抑制作用,包括趋化因子(CC基序)配体(CCL)-2,CCL-3,CCL-5和分泌的肿瘤坏死因子受体1,其中CCL-5表现出明显的抑制作用。细胞和临床GLM标本中的抑制率最高。总体而言,结果表明,BM是体内和体外的新型有效抗炎药,CCL-5可能与GLM发病机理密切相关。

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