Josie A Shapiro, Tapas Bhattacharyya, Lauren A Squire, Christiane L Mallett, Jeremy M-L Hix, Legend E Kenney, Aitor Aguirre, Erik M Shapiro
{"title":"去钓鱼!斑马鱼对临床肝特异性钆基MRI造影剂的肝脏摄取与人类相似。","authors":"Josie A Shapiro, Tapas Bhattacharyya, Lauren A Squire, Christiane L Mallett, Jeremy M-L Hix, Legend E Kenney, Aitor Aguirre, Erik M Shapiro","doi":"10.1007/s11307-025-02023-2","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>Zebrafish are a useful organism for investigating liver disease due to their genetic similarities with humans, particularly in genes associated with liver function. It has been posited that liver function can be assessed non-invasively by MRI, measuring the hepatic accumulation of gadolinium-based contrast agents (GBCAs). We characterized the hepatic uptake of various hepatospecific and non-hepatospecific clinical GBCAs in zebrafish.</p><p><strong>Procedures: </strong>To introduce GBCAs systemically, zebrafish swam for 30 min in water containing 5 mM of various clinical hepatospecific or non-hepatospecific GBCAs. Fish were then sacrificed and underwent 3D, T1-weighted, high-resolution MRI at 9.4 T. In vitro MRI and transport studies of the same GBCAs were conducted in HEK293T cells transiently expressing OATP1D1, OATP1B2 and OATP1B3.</p><p><strong>Results: </strong>T1-weighted ex-vivo MRI of zebrafish showed hyperintensity in the liver, gall bladder, bile ducts, and intestine for fish swimming in gadoxetate, but not for in gadobenate nor gadoterate. In vitro cell experiments confirm that gadoxetate but not gadobenate is efficiently transported by OATP1D1.</p><p><strong>Conclusion: </strong>Zebrafish liver accumulates gadoxetate but not gadobenate via OATP1D1 transport, among the two clinical hepatospecific MRI GBCAs, and also does not accumulate gadoterate, a non-hepatospecific GBCA. This pattern of GBCA hepatic uptake is similar to humans but differs from all other non-primates reported, which exhibit high hepatic uptake of both gadoxetate and gadobenate.</p>","PeriodicalId":18760,"journal":{"name":"Molecular Imaging and Biology","volume":" ","pages":"499-505"},"PeriodicalIF":2.5000,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12405032/pdf/","citationCount":"0","resultStr":"{\"title\":\"Go Fish! 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We characterized the hepatic uptake of various hepatospecific and non-hepatospecific clinical GBCAs in zebrafish.</p><p><strong>Procedures: </strong>To introduce GBCAs systemically, zebrafish swam for 30 min in water containing 5 mM of various clinical hepatospecific or non-hepatospecific GBCAs. Fish were then sacrificed and underwent 3D, T1-weighted, high-resolution MRI at 9.4 T. In vitro MRI and transport studies of the same GBCAs were conducted in HEK293T cells transiently expressing OATP1D1, OATP1B2 and OATP1B3.</p><p><strong>Results: </strong>T1-weighted ex-vivo MRI of zebrafish showed hyperintensity in the liver, gall bladder, bile ducts, and intestine for fish swimming in gadoxetate, but not for in gadobenate nor gadoterate. In vitro cell experiments confirm that gadoxetate but not gadobenate is efficiently transported by OATP1D1.</p><p><strong>Conclusion: </strong>Zebrafish liver accumulates gadoxetate but not gadobenate via OATP1D1 transport, among the two clinical hepatospecific MRI GBCAs, and also does not accumulate gadoterate, a non-hepatospecific GBCA. This pattern of GBCA hepatic uptake is similar to humans but differs from all other non-primates reported, which exhibit high hepatic uptake of both gadoxetate and gadobenate.</p>\",\"PeriodicalId\":18760,\"journal\":{\"name\":\"Molecular Imaging and Biology\",\"volume\":\" \",\"pages\":\"499-505\"},\"PeriodicalIF\":2.5000,\"publicationDate\":\"2025-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12405032/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Molecular Imaging and Biology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1007/s11307-025-02023-2\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/6/3 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Imaging and Biology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s11307-025-02023-2","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/6/3 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING","Score":null,"Total":0}
Go Fish! Hepatic Uptake of Clinical Hepatospecific Gadolinium-Based MRI Contrast Agents in Zebrafish is Similar to Humans.
Purpose: Zebrafish are a useful organism for investigating liver disease due to their genetic similarities with humans, particularly in genes associated with liver function. It has been posited that liver function can be assessed non-invasively by MRI, measuring the hepatic accumulation of gadolinium-based contrast agents (GBCAs). We characterized the hepatic uptake of various hepatospecific and non-hepatospecific clinical GBCAs in zebrafish.
Procedures: To introduce GBCAs systemically, zebrafish swam for 30 min in water containing 5 mM of various clinical hepatospecific or non-hepatospecific GBCAs. Fish were then sacrificed and underwent 3D, T1-weighted, high-resolution MRI at 9.4 T. In vitro MRI and transport studies of the same GBCAs were conducted in HEK293T cells transiently expressing OATP1D1, OATP1B2 and OATP1B3.
Results: T1-weighted ex-vivo MRI of zebrafish showed hyperintensity in the liver, gall bladder, bile ducts, and intestine for fish swimming in gadoxetate, but not for in gadobenate nor gadoterate. In vitro cell experiments confirm that gadoxetate but not gadobenate is efficiently transported by OATP1D1.
Conclusion: Zebrafish liver accumulates gadoxetate but not gadobenate via OATP1D1 transport, among the two clinical hepatospecific MRI GBCAs, and also does not accumulate gadoterate, a non-hepatospecific GBCA. This pattern of GBCA hepatic uptake is similar to humans but differs from all other non-primates reported, which exhibit high hepatic uptake of both gadoxetate and gadobenate.
期刊介绍:
Molecular Imaging and Biology (MIB) invites original contributions (research articles, review articles, commentaries, etc.) on the utilization of molecular imaging (i.e., nuclear imaging, optical imaging, autoradiography and pathology, MRI, MPI, ultrasound imaging, radiomics/genomics etc.) to investigate questions related to biology and health. The objective of MIB is to provide a forum to the discovery of molecular mechanisms of disease through the use of imaging techniques. We aim to investigate the biological nature of disease in patients and establish new molecular imaging diagnostic and therapy procedures.
Some areas that are covered are:
Preclinical and clinical imaging of macromolecular targets (e.g., genes, receptors, enzymes) involved in significant biological processes.
The design, characterization, and study of new molecular imaging probes and contrast agents for the functional interrogation of macromolecular targets.
Development and evaluation of imaging systems including instrumentation, image reconstruction algorithms, image analysis, and display.
Development of molecular assay approaches leading to quantification of the biological information obtained in molecular imaging.
Study of in vivo animal models of disease for the development of new molecular diagnostics and therapeutics.
Extension of in vitro and in vivo discoveries using disease models, into well designed clinical research investigations.
Clinical molecular imaging involving clinical investigations, clinical trials and medical management or cost-effectiveness studies.