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微计算机断层扫描衍生的通气生物标志物用于肺纤维化小鼠模型的病理学纵向评估和治疗反应。

Micro-CT-derived ventilation biomarkers for the longitudinal assessment of pathology and response to therapy in a mouse model of lung fibrosis.

机构信息

Dipartimento di Elettronica, Informazione e Bioingegneria, Politecnico di Milano, Milano, Italy.

Department of Medicine and Surgery, University of Parma, Parma, Italy.

出版信息

Sci Rep. 2023 Mar 17;13(1):4462. doi: 10.1038/s41598-023-30402-8.

Abstract

Experimental in-vivo animal models are key tools to investigate the pathogenesis of lung disease and to discover new therapeutics. Histopathological and biochemical investigations of explanted lung tissue are currently considered the gold standard, but they provide space-localized information and are not amenable to longitudinal studies in individual animals. Here, we present an imaging procedure that uses micro-CT to extract morpho-functional indicators of lung pathology in a murine model of lung fibrosis. We quantified the decrease of lung ventilation and measured the antifibrotic effect of Nintedanib. A robust structure-function relationship was revealed by cumulative data correlating micro-CT with histomorphometric endpoints. The results highlight the potential of in-vivo micro-CT biomarkers as novel tools to monitor the progression of inflammatory and fibrotic lung disease and to shed light on the mechanism of action of candidate drugs. Our platform is also expected to streamline translation from preclinical studies to human patients.

摘要

实验性体内动物模型是研究肺部疾病发病机制和发现新疗法的重要工具。目前,对离体肺组织进行组织病理学和生化研究被认为是金标准,但它们提供的是局部空间信息,并且不适合对个体动物进行纵向研究。在这里,我们提出了一种使用 micro-CT 提取肺纤维化小鼠模型中肺病理学形态功能指标的成像程序。我们量化了肺通气的减少,并测量了尼达尼布的抗纤维化作用。通过将 micro-CT 与组织形态学终点相关联的累积数据,揭示了稳健的结构-功能关系。结果突出了体内 micro-CT 生物标志物作为监测炎症性和纤维性肺病进展以及阐明候选药物作用机制的新型工具的潜力。我们的平台还预计将简化从临床前研究到人类患者的转化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f3c/10023700/8c8eca0bc3a7/41598_2023_30402_Fig1_HTML.jpg

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