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[青藤碱通过阻断大鼠miR-21/ADAMTS-1信号通路改善博来霉素A5诱导的肺纤维化]

[Sinomenine ameliorates bleomycin A5-induced pulmonary fibrosis by blocking the miR-21/ADAMTS-1 signaling pathway in rats].

作者信息

Liu Lijing, Qian Hong, Meng Qingxin, Zhang Xiang, Wei Yingmin, He Jianbin

机构信息

Department of Clinical Medicine, School of Medicine, Changsha Social Work College, Changsha 410004; Department of Respiratory and Critical Care Medicine, First People's Hospital of Huaihua, The Fourth Affiliated Hospital of Jishou University, Huaihua 418000, China.

Department of Clinical Medicine, School of Medicine, Changsha Social Work College, Changsha 410004, China.

出版信息

Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2023 Aug;39(8):721-728.

Abstract

Objective To explore the impact of sinomenine on bleomycin A5-induced pulmonary fibrosis (PF) in rats and the underlying mechanism. Methods MRC-5 cells were cultured and treated with sinomenine to determine its optimal concentration and time through the MTT assay. Subsequently, MRC-5 cells were incubated with 80 μmol/L sinomenine for 48 hours or transfected with miR-21 mimic/a disintegrin-like and metalloproteinase with thrombospondin type 1 motif (ADAMTS-1) siRNA prior to sinomenine treatment. The expression of miR-21, ADAMTS-1, collagen type 1 (Col1) and collagen type 3 (Col3) was detected by quantitative real-time PCR (qRT-PCR) and/or Western blot analysis. Thirty SD rats were randomly divided into control group, sinomenine group and sinomenine combined with miR-21 agomir group, with 10 animals in each group. Bleomycin A5 were intratracheally administered to establish the PF model. Then, rats in control group, sinomenine group and sinomenine +miR-21 agomir group were treated with 9 g/L sodium chloride solution, sinomenine and sinomenine+miR-21 agomir, respectively. On day 28, all rats were sacrificed. HE and Masson staining was performed in pulmonary tissue. The expression of ADAMTS-1, Col1 and Col3 in pulmonary tissue were detected by qRT-PCR and/or Western blot analysis. ELISA was used to measure serum procollagen type 1 carboxyterminal propeptide (P1CP) and procollagen type 3 aminoterminal propeptide (P3NP) levels. Results Administration of sinomenine decreased miR-21 levels, up-regulated ADAMTS-1 expression, and promoted Col1 and Col3 degradation in MRC-5 cells. Importantly, interfering with the miR-21/ADAMTS-1 signaling pathway partially reversed the promotive effect of sinomenine on Col1 and Col3 degradation. Treatment of SD rats with sinomenine reduced alveolitis and PF scores, decreased serum P1CP and P3NP levels, up-regulated pulmonary ADAMTS-1 expression, and down-regulated Col1 and Col3 expression. However, these effects were reversed by miR-21 agomir. Conclusion Sinomenine promotes Col1 and Col3 degradation and inhibits PF in rats by miR-21/ADAMTS-1 pathway.

摘要

目的 探讨青藤碱对博来霉素A5诱导的大鼠肺纤维化(PF)的影响及其潜在机制。方法 培养MRC-5细胞,用青藤碱处理,通过MTT法确定其最佳浓度和时间。随后,将MRC-5细胞与80 μmol/L青藤碱孵育48小时,或在青藤碱处理前用miR-21模拟物/含血小板反应蛋白基序的解整合素样金属蛋白酶(ADAMTS-1)小干扰RNA转染。通过定量实时聚合酶链反应(qRT-PCR)和/或蛋白质免疫印迹分析检测miR-21、ADAMTS-1、Ⅰ型胶原(Col1)和Ⅲ型胶原(Col3)的表达。将30只SD大鼠随机分为对照组、青藤碱组和青藤碱联合miR-21激动剂组,每组10只。经气管内给予博来霉素A5建立PF模型。然后,对照组、青藤碱组和青藤碱+miR-21激动剂组的大鼠分别用9 g/L氯化钠溶液、青藤碱和青藤碱+miR-21激动剂处理。在第28天,处死所有大鼠。对肺组织进行苏木精-伊红(HE)和Masson染色。通过qRT-PCR和/或蛋白质免疫印迹分析检测肺组织中ADAMTS-1、Col1和Col3的表达。采用酶联免疫吸附测定(ELISA)法检测血清Ⅰ型前胶原羧基端前肽(P1CP)和Ⅲ型前胶原氨基端前肽(P3NP)水平。结果 给予青藤碱可降低MRC-5细胞中miR-21水平,上调ADAMTS-1表达,并促进Col1和Col3降解。重要的是,干扰miR-21/ADAMTS-1信号通路可部分逆转青藤碱对Col1和Col3降解的促进作用。用青藤碱处理SD大鼠可降低肺泡炎和PF评分,降低血清P1CP和P3NP水平,上调肺组织中ADAMTS-1表达,并下调Col1和Col3表达。然而,miR-21激动剂可逆转这些作用。结论 青藤碱通过miR-21/ADAMTS-1途径促进大鼠Col1和Col3降解并抑制PF。

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