Shandong University of Traditional Chinese Medicine, No. 4655, Daxue Road, University Science Park, Changqing District, Jinan City, 250355, China.
Affiliated Hospital of Shandong University of Traditional Chinese Medicine, No. 16369, Jing Shi Road, Jinan City, 250013, China.
BMC Pulm Med. 2023 Sep 4;23(1):325. doi: 10.1186/s12890-023-02601-6.
Idiopathic pulmonary fibrosis (IPF), a chronic progressive interstitial lung disease of unknown etiology, is characterized by continuous damage to alveolar epithelial cells, abnormal repair of alveolar tissue, and alveolar wall scar formation. Currently, the recommended treatment for IPF in Western medicine is relatively limited. In contrast, traditional Chinese medicine and compound prescriptions show advantages in the diagnosis and treatment of IPF, which can be attributed to their multi-channel and multi-target characteristics and minimal side-effects. The purpose of this study was to further corroborate the effectiveness and significance of the traditional Chinese medications Astragalus and Danshen in IPF treatment.
We performed whole-genome methylation analysis on nine rat lung tissue samples to determine the epigenetic variation between IPF and non-fibrotic lungs using Gene Ontology and Kyoto Encyclopedia of Genes and Genomes pathway enrichment analyses and quantitative reverse transcription polymerase chain reactions.
We identified differentially methylated regions and 105 associated key functional genes in samples related to IPF and Chinese medicine treatment. Based on the methylation levels and gene expression profiles between the Chinese medicine intervention and pulmonary fibrosis model groups, we speculated that Astragalus and Salvia miltiorrhiza (traditionally known as Danshen) act on the Isl1, forkhead box O3, and Sonic hedgehog genes via regulation at transcriptional and epigenetic levels during IPF.
These findings provide novel insights into the epigenetic regulation of IPF, indicate the effectiveness of Astragalus and Danshen in treating IPF, and suggest several promising therapeutic targets for preventing and treating IPF.
特发性肺纤维化(IPF)是一种病因不明的慢性进行性间质性肺疾病,其特征为肺泡上皮细胞持续损伤、肺泡组织异常修复以及肺泡壁瘢痕形成。目前,西医推荐的 IPF 治疗方法相对有限。相比之下,中药和复方制剂在 IPF 的诊断和治疗中显示出优势,这归因于它们的多途径和多靶点特性以及最小的副作用。本研究旨在进一步证实中药黄芪和丹参在 IPF 治疗中的有效性和意义。
我们对 9 个大鼠肺组织样本进行全基因组甲基化分析,通过基因本体论和京都基因与基因组百科全书通路富集分析以及定量逆转录聚合酶链反应,确定 IPF 与非纤维化肺之间的表观遗传变异。
我们在与 IPF 和中药治疗相关的样本中确定了差异甲基化区域和 105 个相关关键功能基因。基于中药干预组和肺纤维化模型组之间的甲基化水平和基因表达谱,我们推测黄芪和丹参通过在转录和表观遗传水平上调节 Isl1、叉头框 O3 和 Sonic hedgehog 基因来发挥作用在 IPF 中。
这些发现为 IPF 的表观遗传调控提供了新的见解,表明黄芪和丹参在治疗 IPF 中的有效性,并为预防和治疗 IPF 提供了几个有前途的治疗靶点。