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大豆苷元通过降低博莱霉素诱导的实验性肺纤维化中蛋白酶激活受体2的表达以及TGFβ1/smad介导的炎症和凋亡,表现出抗纤维化作用。

Daidzein exhibits anti-fibrotic effect by reducing the expressions of Proteinase activated receptor 2 and TGFβ1/smad mediated inflammation and apoptosis in Bleomycin-induced experimental pulmonary fibrosis.

作者信息

Soumyakrishnan Syamala, Divya Thomas, Kalayarasan Srinivasan, Sriram Narayanan, Sudhandiran Ganapasam

机构信息

Cell Biology Laboratory, Department of Biochemistry, University of Madras, Guindy Campus, Chennai 600 025, India.

Cell Biology Laboratory, Department of Biochemistry, University of Madras, Guindy Campus, Chennai 600 025, India.

出版信息

Biochimie. 2014 Aug;103:23-36. doi: 10.1016/j.biochi.2014.04.005. Epub 2014 Apr 24.

Abstract

Pulmonary fibrosis (PF) is a progressive lethal disorder. In this study, the effect of daidzein, a soyisoflavone against Bleomycin (BLM) induced PF in rats was elucidated. A single intratracheal instillation of BLM (3 U/kg.bw) was administered in rats to induce PF. Daidzein (0.2 mg/kg) was administered subcutaneously, twice a week for a period of 28 days. Daidzein restored the histological alteration and aberrant collagen deposition, suppressed the mast cells, and reduced the expressions of Cyclooxygenase 2 (COX2) and Nuclear factor kappa B (Nf-kB) in lung tissue of BLM-induced rats. Treatment with daidzein reduced the expression of Matrix metalloproteinase 2 (MMP-2) and increased the expression of Tissue inhibitor of matrixmetalloproteinases 1 (TIMP 1). Recently, Proteinase activated receptor 2 (PAR2) has been reported to play a major role in the progression of PF. Confocal microscopic and immunoblot analysis revealed that BLM injured rat lungs exhibited increased expression of PAR2 that was reduced upon treatment with daidzein. During BLM induction, Transforming growth factor beta (TGFβ1) was found to be up-regulated along with p-smad2/3, a mediator of TGFβ signaling. Further, daidzein regulated the apoptosis by modulating the expressions of Bcl-2, Bax and caspase 3. This study provides evidence on the anti-fibrotic role of daidzein in BLM-induced experimental fibrosis.

摘要

肺纤维化(PF)是一种进行性致死性疾病。在本研究中,阐明了大豆异黄酮黄豆苷元对博来霉素(BLM)诱导的大鼠肺纤维化的影响。向大鼠气管内单次注入BLM(3 U/kg体重)以诱导肺纤维化。黄豆苷元(0.2 mg/kg)皮下给药,每周两次,持续28天。黄豆苷元恢复了组织学改变和异常的胶原沉积,抑制了肥大细胞,并降低了BLM诱导的大鼠肺组织中环氧合酶2(COX2)和核因子κB(Nf-κB)的表达。黄豆苷元治疗降低了基质金属蛋白酶2(MMP-2)的表达并增加了基质金属蛋白酶组织抑制剂1(TIMP 1)的表达。最近,据报道蛋白酶激活受体2(PAR2)在PF进展中起主要作用。共聚焦显微镜和免疫印迹分析显示,BLM损伤的大鼠肺中PAR2表达增加,而黄豆苷元治疗后PAR2表达降低。在BLM诱导过程中,发现转化生长因子β(TGFβ1)与TGFβ信号传导介质p-smad2/3一起上调。此外,黄豆苷元通过调节Bcl-2、Bax和半胱天冬酶3的表达来调节细胞凋亡。本研究提供了黄豆苷元在BLM诱导的实验性纤维化中的抗纤维化作用的证据。

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