Suppr超能文献

基于 X 射线的纵向肺功能测量用于监测肺纤维化小鼠模型中尼达尼布的治疗反应。

Longitudinal x-ray based lung function measurement for monitoring Nintedanib treatment response in a mouse model of lung fibrosis.

机构信息

Translational Molecular Imaging, Max Planck Institute for Multidisciplinary Sciences, Göttingen, Germany.

Cluster of Excellence "Multiscale Bioimaging: from Molecular Machines to Networks of Excitable Cells" (MBExC), Göttingen, Germany.

出版信息

Sci Rep. 2023 Oct 30;13(1):18637. doi: 10.1038/s41598-023-45305-x.

Abstract

Lung fibrosis (LF) is a chronic progressive, incurable, and debilitating condition of the lung, which is associated with different lung disease. Treatment options are still sparse. Nintedanib, an oral tyrosine kinase inhibitor, significantly slows the LF progression. However, there is a strong need of further research and the development of novel therapies. In this study, we used a correlative set-up that combines X-ray based lung function (XLF) with microCT and whole body plethysmography (WBP) for a comprehensive functional and structural evaluation of lung fibrosis (LF) as well as for monitoring response to orally administered Nintedanib in the mouse model of bleomycin induced LF. The decline in lung function as early as one week after intratracheal bleomycin instillation was reliably detected by XLF, revealing the lowest decay rate in the LF mice compared to healthy ones. Simultaneously performed microCT and WBP measurements corroborated XLF findings by exhibiting reduced lung volume [Formula: see text] and tidal volume [Formula: see text]. In LF mice XLF also revealed profound improvement in lung function one week after Nintedanib treatment. This positive response to Nintedanib therapy was further substantiated by microCT and WBP measurements which also showed significantly improved [Formula: see text] and [Formula: see text] in the Nintedanib treated mice. By comparing the XLF data to structural features assessing the extent of fibrosis obtained by ex-vivo high-resolution synchrotron radiation-based imaging and classical histology we demonstrate that: (1) a simple low dose x-ray measurement like XLF is sensitive enough to pick up treatment response, (2) Nintedanib treatment successfully improved lung function in a bleomycin induced LF mouse model and (3) differences between the fully restored lung function and the partially reduced fibrotic burden compared to healthy and untreated mice. The presented analysis pipeline underlines the importance of a combined functional and anatomical readout to reliably measure treatment response and could easily be adapted to other preclinical lung disease models.

摘要

肺纤维化(LF)是一种慢性进行性、无法治愈且使人虚弱的肺部疾病,与不同的肺部疾病有关。治疗选择仍然很少。尼达尼布,一种口服酪氨酸激酶抑制剂,显著减缓 LF 的进展。然而,仍然需要进一步的研究和新型疗法的开发。在这项研究中,我们使用了一种相关的设置,将基于 X 射线的肺功能(XLF)与 microCT 和全身 plethysmography(WBP)相结合,对肺纤维化(LF)进行全面的功能和结构评估,以及监测口服尼达尼布在博莱霉素诱导的 LF 小鼠模型中的反应。通过 XLF 可靠地检测到气管内博莱霉素滴注后一周肺功能的早期下降,与健康对照组相比,LF 小鼠的下降率最低。同时进行的 microCT 和 WBP 测量通过显示减少的肺容量 [公式:见文本] 和潮气量 [公式:见文本] 证实了 XLF 的发现。在 LF 小鼠中,尼达尼布治疗一周后,XLF 也显示出肺功能的显著改善。通过 microCT 和 WBP 测量也证实了尼达尼布治疗的这种积极反应,这些测量还显示出尼达尼布治疗的小鼠 [Formula: see text] 和 [Formula: see text] 显著改善。通过将 XLF 数据与通过体外高分辨率同步辐射成像和经典组织学获得的评估纤维化程度的结构特征进行比较,我们证明:(1)像 XLF 这样简单的低剂量 X 射线测量足以发现治疗反应,(2)尼达尼布治疗成功改善了博莱霉素诱导的 LF 小鼠模型中的肺功能,(3)与健康和未治疗的小鼠相比,完全恢复的肺功能与部分减少的纤维化负担之间的差异。所提出的分析流程强调了功能和解剖学综合读数的重要性,以可靠地测量治疗反应,并且可以轻松适应其他临床前肺部疾病模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/525a/10616088/6e6a61d155d9/41598_2023_45305_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验