ArticlePhotoacoustics2025
Quantitative longitudinal investigation of non-alcoholic steatohepatitis in mice by photoacoustic microscopy.
Article in Photoacoustics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed.
- Review
- Photoacoustic Microscopy for Multiscale Biological System Visualization and Clinical Translation.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026Review
- Label-free photoacoustic imaging of glassfrog development.Photoacoustics · 2025Article
- Optical imaging unveils morphological heterogeneity at the hepatic lobule level during metabolic dysfunction-associated fatty liver disease progression [Invited].Biomedical optics express · 2025Article
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Authors and funding
10 authors.
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Abstract
Non-alcoholic steatohepatitis (NASH) is a prevalent chronic liver disease characterized by significant alterations in liver microvascular structures, leading to microcirculatory dysfunction and potentially contributing to various extrahepatic complications. In this study, we propose a longitudinal investigative pipeline based on liver photoacoustic microscopy (LPAM), integrating optical-resolution photoacoustic microscopy (OR-PAM), a modular liver window (MLW), a custom 3D-printed liver imaging mount (LIM), and a dedicated vessel-sinusoid separation and analysis method. This pipeline enabled continuous monitoring and quantitative assessment of microvascular changes in a NASH mouse model over a six-week period. As NASH progressed, vessel density decreased by 64.18 %, and hepatic sinusoid vessel coverage was reduced by 77.38 %. Furthermore, hepatic sinusoidal volume, length, radius, tortuosity, and density declined by 87.29 %, 83.92 %, 21.86 %, 71.57 %, and 86.81 %, Analysis of hepatic sinusoidal branches revealed a 51.80 % decrease in the fractal dimension of composite branches and a 54.90 % increase in that of dead-end branches. These findings suggest that lipid accumulation and inflammatory responses contribute to the progressive deterioration of hepatic microvascular structures, thereby exacerbating vascular damage. LPAM offers a high-resolution, label-free imaging approach for dynamic monitoring of NASH-associated microvascular alterations. This study advances our understanding of hepatic microcirculatory changes in NASH and provides valuable insights for both basic research and clinical management.
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