Use of [18F]FDG/PET to access the rosmarinic acid anti-inflammatory effect in a mouse sponge implant model

Authors

  • Schirmer, B.G.A. Centro de Desenvolvimento da Tecnologia Nuclear - CDTN https://orcid.org/0000-0003-2676-5573
  • Dornelas, I. C. D. Centro de Desenvolvimento da Tecnologia Nuclear - CDTN
  • Ferreira, L. de C. A Centro de Desenvolvimento da Tecnologia Nuclear - CDTN
  • Marques, J. V. R Centro de Desenvolvimento da Tecnologia Nuclear - CDTN
  • Souza, M. D. Centro de Desenvolvimento da Tecnologia Nuclear - CDTN
  • Miranda, M. B. Universidade Federal de Minas Gerais - UFMG
  • Castro, P. R. Universidade Federal de Minas Gerais - UFMG
  • Pereira, J. M Centro de Desenvolvimento da Tecnologia Nuclear - CDTN
  • Barcelos, L.S. Universidade Federal de Minas Gerais - UFMG
  • Malamut, C. Centro de Desenvolvimento da Tecnologia Nuclear

DOI:

https://doi.org/10.15392/2319-0612.2024.2490

Keywords:

[18F]FDG, anti-inflammatory agents, rosmarinic acid, sponge model, MicroPET

Abstract

Positron emission tomography (PET) is one of the most sensitive and effective imaging techniques for detecting very low concentrations of specific radiotracers. It is suitable for analyzing biochemical, metabolic, physiological and functional information at the molecular level in vivo and non-invasively. PET using 2-deoxy-2[18F]-fluoro-D-glucose ([18F]FDG) can be used to identify sites of inflammation and other pathologies and to monitor the efficacy of treatment. This technique can be used to study the effect of rosmarinic acid (RA) in various preclinical models. RA is a natural compound with promising antioxidant and anti-inflammatory effects. Therefore, the aim of this study is to investigate the anti-inflammatory potential of RA and the efficacy of PET/[18F]FDG in localizing inflammation and assessing response to treatment. A sponge implant model in mice was used for this purpose. All experiments were performed with male BALB/c mice aged 6 to 9 weeks and weighing 18 to 22 g, with 5 animals per group (10 animals in total throughout the study). Methods: The mice were implanted with sponge-like polyurethane discs to induce local inflammation. The animals were divided into two experimental groups: those treated with a vehicle and those treated with RA. PET scans with [18F]FDG were performed to evaluate the inflammatory process. Results: The results obtained with [18F]FDG showed a decrease in inflammatory cell infiltrates in the sponge after treatment with RA. Conclusion: The use of [18F]FDG demonstrated its efficacy in quantitatively evaluating the inflammatory process in the mouse subcutaneous sponge model as well as the anti-inflammatory effect of RA.

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Author Biographies

  • Schirmer, B.G.A., Centro de Desenvolvimento da Tecnologia Nuclear - CDTN

    Centro de Desenvolvimento da Tecnologia Nuclear (CDTN), Unidade de Pesquisa e Produção de Radiofármacos

  • Dornelas, I. C. D., Centro de Desenvolvimento da Tecnologia Nuclear - CDTN

    Centro de Desenvolvimento da Tecnologia Nuclear (CDTN), Unidade de Pesquisa e Produção de Radiofármacos

  • Ferreira, L. de C. A, Centro de Desenvolvimento da Tecnologia Nuclear - CDTN

    Centro de Desenvolvimento da Tecnologia Nuclear (CDTN), Unidade de Pesquisa e Produção de Radiofármacos

  • Marques, J. V. R, Centro de Desenvolvimento da Tecnologia Nuclear - CDTN

    Centro de Desenvolvimento da Tecnologia Nuclear (CDTN), Unidade de Pesquisa e Produção de Radiofármacos

  • Souza, M. D., Centro de Desenvolvimento da Tecnologia Nuclear - CDTN

    Centro de Desenvolvimento da Tecnologia Nuclear (CDTN), Unidade de Pesquisa e Produção de Radiofármacos

  • Miranda, M. B., Universidade Federal de Minas Gerais - UFMG

    Department of Physiology, Biological Science Institute, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.

  • Castro, P. R., Universidade Federal de Minas Gerais - UFMG

    Department of Physiology, Biological Science Institute, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.

  • Pereira, J. M, Centro de Desenvolvimento da Tecnologia Nuclear - CDTN

    Centro de Desenvolvimento da Tecnologia Nuclear (CDTN), Unidade de Pesquisa e Produção de Radiofármacos

  • Barcelos, L.S., Universidade Federal de Minas Gerais - UFMG

    Department of Physiology, Biological Science Institute, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.

  • Malamut, C., Centro de Desenvolvimento da Tecnologia Nuclear

    Centro de Desenvolvimento da Tecnologia Nuclear (CDTN), Unidade de Pesquisa e Produção de Radiofármacos

References

Li, Y., Wang, Q., Wang, X., Li, X., Wu, H., Wang, Q., & Li, X. F. (2020). Expert Consensus on clinical application of FDG PET/CT in infection and inflammation. Annals of Nuclear Medicine, 34, 369-376.

RAHMAN, W. T. et al. The impact of infection and inflammation in oncologic 18F-FDG PET/CT imaging. Biomedecine & pharmacotherapie [Biomedicine & pharmacotherapy], v. 117, n. 109168, p. 109168, 2019.

JAMAR, F. et al. EANM/SNMMI guideline for18F-FDG use in inflammation and infection. Journal of Nuclear Medicine, v. 54, n. 4, p. 647–658, 2013.

CALDER, P. C.; DIMITRIADIS, G.; NEWSHOLME, P. Glucose metabolism in lymphoid and inflammatory cells and tissues. Current opinion in clinical nutrition and metabolic care, v. 10, n. 4, p. 531–540, 2007.

MARTINEAU, P. et al. Assessing cardiovascular infection and inflammation with FDG-PET. American Journal of Nuclear Medicine and Molecular Imaging, v. 11, n. 1, p. 46, 2021.

QIAO, S. et al. Rosmarinic acid inhibits the formation of reactive oxygen and nitrogen species in RAW264.7 macrophages. Free radical research, v. 39, n. 9, p. 995–1003, 2009.

YOUN, J. et al. Beneficial effects of rosmarinic acid on suppression of collagen induced arthritis. The journal of rheumatology, v. 30, n. 6, 2003.

LUAN, H. et al. Rosmarinic acid protects against experimental diabetes with cerebral ischemia: relation to inflammation response. Journal of neuroinflammation, v. 10, n. 1, 2013.

ROCHA, J. et al. Anti‐inflammatory effect of rosmarinic acid and an extract of Rosmarinus officinalis in rat models of local and systemic inflammation. Basic & clinical pharmacology & toxicology, v. 116, n. 5, p. 398–413, 2015.

PEREIRA, J. M. et al. Use of [18F]FLT/PET for assessing the tumor evolution and monitoring the antitumor activity of rosmarinic acid in a mouse 4T1 breast tumor model. Brazilian Journal of Radiation Sciences, v. 11, n. 3, p. 01–23, 2023.

FARIA ALMEIDA, F. A. DE et al. KETO[18F]FDG -VAP-P1: In vivo studies of a potential PET radiotracer for diagnosis of inflammation. Applied radiation and isotopes: including data, instrumentation and methods for use in agriculture, industry and medicine, v. 192, n. 110547, p. 110547, 2023.

CASTRO, P. R. et al. Kinetics of implant-induced inflammatory angiogenesis in abdominal muscle wall in mice. Microvascular research, v. 84, n. 1, p. 9–15, 2012.

FERREIRA, M. A. N. D. et al. Sponge‐induced angiogenesis and inflammation in PAF receptor‐deficient mice (PAFR‐KO). British journal of pharmacology, v. 141, n. 7, p. 1185–1192, 2004.

GUABIRABA, R. et al. Blockade of cannabinoid receptors reduces inflammation, leukocyte accumulation and neovascularization in a model of sponge-induced inflammatory angiogenesis. et al [Inflammation research], v. 62, n. 8, p. 811–821, 2013.

CASSINI-VIEIRA, P. et al. Estimation of wound tissue neutrophil and macrophage accumulation by measuring myeloperoxidase (MPO) and N-acetyl-β-D-glucosaminidase (NAG) activities. Bio-protocol, v. 5, n. 22, 2015.

SANTOS, E. V. DOS et al. Applicability of [18F]FDG/PET for investigating rosmarinic acid preconditioning efficacy in a global stroke model in mice. Brazilian Journal of Pharmaceutical Sciences, v. 59, p. e21555, 2023.

LANNA, M. F. et al. Kinetics of phenotypic and functional changes in mouse models of sponge implants: Rational selection to optimize protocols for specific biomolecules screening purposes. Frontiers in bioengineering and biotechnology, v. 8, 2020.

CAO, W. et al. Rosmarinic acid inhibits inflammation and angiogenesis of hepatocellular carcinoma by suppression of NF-κB signaling in H22 tumor-bearing mice. Journal of pharmacological sciences, v. 132, n. 2, p. 131–137, 2016.

JIANG, K. et al. Anti-inflammatory effects of rosmarinic acid in lipopolysaccharide-induced mastitis in mice. Inflammation, v. 41, n. 2, p. 437–448, 2018

HUANG, S.-S.; ZHENG, R.-L. Rosmarinic acid inhibits angiogenesis and its mechanism of action in vitro. Cancer letters, v. 239, n. 2, p. 271–280, 2006.

ANDRADE, S. P.; FERREIRA, M. A. N. D. The sponge implant model of angiogenesis. Em: Methods in Molecular Biology. New York, NY: Springer New York, 2016. v. 1430p. 333–343.

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Published

2024-10-11

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How to Cite

Use of [18F]FDG/PET to access the rosmarinic acid anti-inflammatory effect in a mouse sponge implant model. Brazilian Journal of Radiation Sciences, Rio de Janeiro, Brazil, v. 12, n. 4, 2024. DOI: 10.15392/2319-0612.2024.2490. Disponível em: https://bjrs.org.br/revista/index.php/REVISTA/article/view/2490.. Acesso em: 15 oct. 2024.

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