Early diagnosis and staging of paraquat-induced pulmonary fibrosis using [18F]F-FAPI-42 PET/CT imaging

被引:5
作者
Zhang, Dimei [1 ]
Shi, Yusheng [4 ]
Kong, Jiangwei [3 ]
Chen, Na [5 ]
Li, Guiting [6 ]
Wang, Mingfang [6 ]
Zhang, Guoxia [1 ]
Zhai, Chuangyan [2 ,3 ]
机构
[1] Southern Med Univ, Sch Publ Hlth, Guangdong Prov Key Lab Trop Dis Res, Guangzhou 510515, Peoples R China
[2] Southern Med Univ, Nanfang Hosp, Dept Nucl Med, Guangzhou 510515, Peoples R China
[3] Southern Med Univ, Sch Forens Med, Guangzhou 510515, Peoples R China
[4] Jinan Univ, Zhuhai Peoples Hosp, Zhuhai Hosp, Dept Radiat Oncol, Zhuhai 519000, Peoples R China
[5] Guangdong Women & Children Hosp, Dept Pathol, Guangzhou 511400, Peoples R China
[6] Guangdong Huixuan Pharmaceut Technol Co Ltd, Res & Dev Ctr, Guangzhou 510765, Peoples R China
基金
中国国家自然科学基金;
关键词
F-18]F-FAPI-42; PET/CT; Pulmonary fibrosis; Early diagnosis; Disease staging; MECHANISMS; TOXICITY;
D O I
10.1186/s13550-024-01118-1
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Background Paraquat (PQ) -induced pulmonary fibrosis poses a significant medical challenge due to limited treatment options and high mortality rates. Consequently, there is an urgent need for early diagnosis and accurate staging to facilitate appropriate treatment strategies. In this study, we assessed the diagnostic potential of [F-18]F-FAPI-42 PET/CT imaging for early detection and disease staging in a rat model of PQ-induced lung fibrosis. Methods After administering 80 mg/kg of PQ orally to Sprague-Dawley rats, we intravenously injected 3-3.5 MBq of [F-18]F-FAPI-42 on day 7, 14, and 21 post-dosing. Dynamic PET/CT imaging was carried out for one hour immediately after the administration of [F-18]F-FAPI-42. Subsequently, the lung tissues were collected for Hematoxylin and Eosin (HE) staining, Masson's trichrome staining, and NOTA-FAPI-04-MB fluorescent probe staining. Data analysis was performed using the Imalytics preclinical software, and the mean standardized uptake value (SUVmean) was calculated. Results PET signals revealed that in areas with evident lesions on CT, the SUVmean on day 14 was significantly higher than on day 7 and 21, indicating that changes in fibrosis activity levels contribute to the staging of pulmonary fibrosis. Additionally, the NOTA-FAPI-04-MB fluorescent probe staining also demonstrated the most pronounced probe uptake on day 14. In regions without apparent lesions on CT, the SUVmean gradually increased from day 7 to day 21, reflecting ongoing fibrotic activity. Moreover, HE staining and Masson's trichrome staining did not reveal pulmonary fibrosis, while PET imaging was able to detect it, serving the purpose of early diagnosis. At 30 min and 60 min, the target-to-background ratio (TBR) of the PQ groups on day 7, 14, and 21 was significantly higher than the control group, suggesting a high specificity of [F-18]F-FAPI-42 binding to activated fibroblasts. Conclusion [F-18]F-FAPI-42 PET/CT imaging enables early diagnosis and staging of PQ-induced pulmonary fibrosis, demonstrating its feasibility and potential for characterizing early disease stages.
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页数:12
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共 36 条
[1]   The Latest Developments in Imaging of Fibroblast Activation Protein [J].
Altmann, Annette ;
Haberkorn, Uwe ;
Siveke, Jens .
JOURNAL OF NUCLEAR MEDICINE, 2021, 62 (02) :160-167
[2]   Paraquat research: do recent advances in limiting its toxicity make its use safer? [J].
Baltazar, Teresa ;
Dinis-Oliveira, Ricardo Jorge ;
Duarte, Jose Alberto ;
Bastos, Maria de Lourdes ;
Carvalho, Felix .
BRITISH JOURNAL OF PHARMACOLOGY, 2013, 168 (01) :44-45
[3]   5-Aminosalicylic acid attenuates paraquat-induced lung fibroblast activation and pulmonary fibrosis of rats [J].
Chen, Hui ;
Cui, Jinfeng ;
Wang, Juan ;
Wang, Yuan ;
Tong, Fei ;
Tian, Yingping ;
Gong, Yu ;
Ma, Yu ;
Liu, Liang ;
Zhang, Xianghong .
MOLECULAR MEDICINE REPORTS, 2022, 25 (02)
[4]   Presentation, diagnosis and clinical course of the spectrum of progressive-fibrosing interstitial lung diseases [J].
Cottin, Vincent ;
Hirani, Nikhil A. ;
Hotchkin, David L. ;
Nambiar, Anoop M. ;
Ogura, Takashi ;
Otaola, Maria ;
Skowasch, Dirk ;
Park, Jong Sun ;
Poonyagariyagorn, Hataya K. ;
Wuyts, Wim ;
Wells, Athol U. .
EUROPEAN RESPIRATORY REVIEW, 2018, 27 (150)
[5]   Progress Toward Improving Animal Models for Idiopathic Pulmonary Fibrosis [J].
Degryse, Amber L. ;
Lawson, William E. .
AMERICAN JOURNAL OF THE MEDICAL SCIENCES, 2011, 341 (06) :444-449
[6]   Paraquat poisonings:: Mechanisms of lung toxicity, clinical features, and treatment [J].
Dinis-Oliveira, R. J. ;
Duarte, J. A. ;
Sanchez-Navarro, A. ;
Remiao, F. ;
Bastos, M. L. ;
Carvalho, F. .
CRITICAL REVIEWS IN TOXICOLOGY, 2008, 38 (01) :13-71
[7]   Common and distinct mechanisms of induced pulmonary fibrosis by particulate and soluble chemical fibrogenic agents [J].
Dong, Jie ;
Yu, Xiaoqing ;
Porter, Dale W. ;
Battelli, Lori A. ;
Kashon, Michael L. ;
Ma, Qiang .
ARCHIVES OF TOXICOLOGY, 2016, 90 (02) :385-402
[8]   Time-resolved proteome and transcriptome of paraquat-induced pulmonary fibrosis [J].
Fan, Lu ;
Li, Yuan ;
Zhang, Xiaomin ;
Wu, Yuxuan ;
Song, Yang ;
Zhang, Feng ;
Zhang, Jinsong ;
Sun, Hao .
PULMONARY PHARMACOLOGY & THERAPEUTICS, 2022, 75
[9]   Overview of positron emission tomography in functional imaging of the lungs for diffuse lung diseases [J].
Gulhane, Avanti V. ;
Chen, Delphine L. .
BRITISH JOURNAL OF RADIOLOGY, 2022, 95 (1132)
[10]   Advancement in Production of Radiotracers [J].
Hansen, Soren Baarsgaard ;
Bender, Dirk .
SEMINARS IN NUCLEAR MEDICINE, 2022, 52 (03) :266-275