Related Experiment Video
Updated: Feb 3, 2026

Establishment and Validation of a Rat Model of Pulmonary Arterial Hypertension Associated with Pulmonary Fibrosis
Published on: May 23, 2025
Apoptotic PET Imaging of Rat Pulmonary Fibrosis With [18F]ML-8
Ying Xiong1, Dahong Nie1, Shaoyu Liu1
11 Guangdong Engineering Research Center for Translational Application of Medical Radiopharmaceuticals and Department of Medical Imaging, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Objective:
To investigate the value of 2-(3-[18F]fluoropropyl)-2-methyl-malonic acid ([18F]ML-8) positron emission tomography (PET) imaging of rat pulmonary fibrosis.
Methods:
Male Sprague-Dawley rats were divided into 2 groups, including pulmonary fibrosis model group and control group. The rat model was established by an intratracheal instillation of bleomycin (BLM). Control rats were treated with saline. Positron emission tomography/computed tomography (CT) with [18F]ML-8 or 18F-fluorodeoxyglucose ([18F]FDG) was performed on 2 groups. After PET/CT imaging, lung tissues were collected for histologic examination. Data were analyzed and comparisons between 2 groups were performed using Student t test.
Results:
Bleomycin-treated rats showed a higher lung uptake of [18F]ML-8 than control rats ( P < .05). In BLM-treated rats, the lung to muscle relative uptake ratio of [18F]ML-8 was also higher than that of [18F]FDG ( P < .05). Pathological examination showed overproliferation of fibroblasts and deposition of collagen in lungs from BLM-treated rats. Compared to control rats, BLM-treated rats had higher lung hydroxyproline content ( P < .05). Immunofluorescence staining indicated more apoptotic cells in BLM-treated rats than those in control rats. Moreover, the apoptosis rate of lung tissues obtained from BLM-treated rats was higher than that from control rats ( P < .05).
Conclusions:
2-(3-[18F]fluoropropyl)-2-methyl-malonic acid PET/CT could be used for noninvasive diagnosis of pulmonary fibrosis in a rat model.
Insights
Positron emission tomography (PET) imaging using 2-(3-[18F]fluoropropyl)-2-methyl-malonic acid ([18F]ML-8) can noninvasively diagnose pulmonary fibrosis in rats. This novel imaging agent shows higher uptake in fibrotic lungs compared to controls.
Area of Science:
- Medical Imaging
- Radiochemistry
- Pulmonary Medicine
Background:
- Pulmonary fibrosis is a progressive lung disease with limited diagnostic tools.
- Noninvasive imaging is crucial for early detection and monitoring of fibrotic lung diseases.
- Developing novel PET tracers is essential for improving diagnostic accuracy.
Purpose of the Study:
- To evaluate the efficacy of 2-(3-[18F]fluoropropyl)-2-methyl-malonic acid ([18F]ML-8) positron emission tomography (PET) for diagnosing rat pulmonary fibrosis.
- To compare the diagnostic performance of [18F]ML-8 PET with [18F]FDG PET in a bleomycin-induced pulmonary fibrosis rat model.
Main Methods:
- A bleomycin (BLM)-induced pulmonary fibrosis rat model was established.
- Rats underwent PET/CT imaging using either [18F]ML-8 or [18F]FDG.
- Lung tissues were analyzed histologically, and hydroxyproline content and apoptosis rates were measured.
Main Results:
- [18F]ML-8 showed significantly higher lung uptake in BLM-treated rats compared to controls (P < .05).
- The lung-to-muscle uptake ratio of [18F]ML-8 was higher than that of [18F]FDG in fibrotic lungs (P < .05).
- Histological analysis confirmed fibroblast proliferation, collagen deposition, and increased apoptosis in BLM-treated rat lungs.
Conclusions:
- [18F]ML-8 PET/CT imaging is a valuable tool for the noninvasive diagnosis of pulmonary fibrosis in a rat model.
- This novel PET tracer demonstrates superior performance compared to [18F]FDG for detecting pulmonary fibrosis.
- Further research may explore [18F]ML-8 for clinical applications in human pulmonary fibrosis.
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