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小檗碱通过抑制 NF-κB 依赖的 TGF-β 激活减轻博来霉素诱导的肺毒性和纤维化:一项双相实验研究。

Berberine attenuates bleomycin induced pulmonary toxicity and fibrosis via suppressing NF-κB dependant TGF-β activation: a biphasic experimental study.

机构信息

Department of Biochemistry, Cell Biology Laboratory, University of Madras, Guindy Campus, Chennai, Tamil Nadu, India.

出版信息

Toxicol Lett. 2013 May 23;219(2):178-93. doi: 10.1016/j.toxlet.2013.03.009. Epub 2013 Mar 21.

Abstract

Idiopathic pulmonary fibrosis (IPF) is a progressive, debilitating and fatal lung disorder with high mortality rate. Unfortunately, to date the treatment for IPF remains unsatisfying and in severe cases lung transplantations are performed as a therapeutic measure. Thus, it becomes great interest to find novel agents to treat IPF. Berberine, a plant alkaloid known for its broad pharmacological activities remains a remedy against multiple diseases. This study was hypothesized to investigate the antifibrotic potential of berberine against bleomycin-induced lung injury and fibrosis, a tentative animal model. Male wistar rats were subjected to single intratracheal instillation of 2.5 U/kg of bleomycin on day 0. Berberine treatments were either provided in preventive or therapeutic mode respectively. Berberine administration significantly ameliorated the bleomycin mediated histological alterations and reduced the inflammatory cell infiltrate in BALF. Berberine significantly blocked collagen accumulations with parallel reduction in the hydroxyproline level. The immunological sign of bleomycin stimulated mast cell deposition and histamine release were considerably reduced by berberine. Berberine enhanced the antioxidant status, through upregulating the redox sensing transcription factor nuclear factor E2-related factor 2 (Nrf2). Berberine inhibited the bleomycin mediated activation of inflammatory mediator nuclear factor kappa B (NF-κB) and suppressed its downstream target inducible nitric oxide synthase (iNOS). Strikingly, berberine exhibited target attenuation of tumor necrosis factor alpha (TNF-α) and key pro-fibrotic mediator, transforming growth factor beta 1 (TGF-β1). Taken together, this study reveals the beneficial effects of berberine against bleomycin mediated fibrotic challenge through activating Nrf2 and suppressing NF-κB dependent inflammatory and TGF-β1 mediated fibrotic events.

摘要

特发性肺纤维化(IPF)是一种进行性、使人虚弱和致命的肺部疾病,死亡率很高。不幸的是,迄今为止,IPF 的治疗仍然不尽如人意,在严重情况下,肺移植作为一种治疗措施。因此,寻找治疗 IPF 的新药物成为人们极大的兴趣。小檗碱是一种植物生物碱,具有广泛的药理活性,一直是治疗多种疾病的药物。本研究假设研究小檗碱对博来霉素诱导的肺损伤和纤维化的抗纤维化潜力,这是一种动物模型。雄性 Wistar 大鼠在第 0 天接受 2.5 U/kg 的博来霉素单次气管内滴注。小檗碱治疗分别以预防或治疗模式提供。小檗碱给药显著改善了博来霉素介导的组织学改变,并减少了 BALF 中的炎症细胞浸润。小檗碱显著阻断胶原积累,同时羟脯氨酸水平降低。博来霉素刺激的肥大细胞沉积和组胺释放的免疫学迹象被小檗碱显著减少。小檗碱通过上调氧化还原感应转录因子核因子 E2 相关因子 2(Nrf2)增强了抗氧化状态。小檗碱抑制了博来霉素介导的炎症介质核因子 kappa B(NF-κB)的激活,并抑制了其下游靶基因诱导型一氧化氮合酶(iNOS)。引人注目的是,小檗碱对肿瘤坏死因子 alpha(TNF-α)和关键的促纤维化介质转化生长因子 beta 1(TGF-β1)表现出靶向衰减。总之,这项研究揭示了小檗碱通过激活 Nrf2 和抑制 NF-κB 依赖性炎症和 TGF-β1 介导的纤维化事件对博来霉素介导的纤维化挑战的有益作用。

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