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https://doi.org/10.1016/j.molmet.2019.05.003
Title: | Imaging adipose tissue browning using the TSPO-18kDa tracer [18F]FEPPA | Authors: | Hartimath, S.V. Khanapur, S. Boominathan, R. Jiang, L. Cheng, P. Yong, F.F. Tan, P.W. Robins, E.G. Goggi, J.L. |
Keywords: | Beige Brown fat FDG PET imaging TSPO-18kDa ?3-adrenergic receptor |
Issue Date: | 2019 | Publisher: | Elsevier GmbH | Citation: | Hartimath, S.V., Khanapur, S., Boominathan, R., Jiang, L., Cheng, P., Yong, F.F., Tan, P.W., Robins, E.G., Goggi, J.L. (2019). Imaging adipose tissue browning using the TSPO-18kDa tracer [18F]FEPPA. Molecular Metabolism 25 : 154-158. ScholarBank@NUS Repository. https://doi.org/10.1016/j.molmet.2019.05.003 | Rights: | Attribution-NonCommercial-NoDerivatives 4.0 International | Abstract: | Objectives: The browning of white adipose tissue (WAT) into beige has been proposed as a strategy to enhance energy expenditure to combat the growing epidemic of obesity. Research into browning strategies are hampered by the lack of sensitive, translatable, imaging tools capable of detecting beige fat mass non-invasively. [18F]FDG is able to detect activated beige fat but provides little information on unstimulated beige fat mass. We have assessed the use of [18F]FEPPA, a tracer for the TSPO-18KDa found on the outer mitochondrial membrane, as an alternative imaging agent capable of detecting unstimulated brown fat (BAT) and beige fat. Methods: Female Balb/c mice (n = 5) were treated for 7 days with the β3 adrenergic agonist CL-316,243 to induce the browning of inguinal WAT (beige fat). Animals were imaged longitudinally with [18F]FDG and [18F]FEPPA and uptake in interscapular BAT and inguinal WAT assessed. The browning of inguinal WAT was confirmed using H&E and immunohistochemical detection of UCP-1 and TSPO. Results: Repeated dosing with β3-adrenergic agonist CL-316,243 caused a significant increase in [18F]FDG uptake in both interscapular BAT and inguinal WAT associated with the increased metabolic activity of brown and beige adipocytes respectively. [18F]FEPPA uptake was likewise increased in inguinal WAT but showed no increase in BAT uptake due to stimulation over the same time course. Furthermore, inguinal WAT uptake was unaffected by pharmacological blockade, indicating that [18F]FEPPA uptake is associated with the expression of mitochondria in BAT and beige adipocytes and independent of activation. Conclusion: These data show that [18F]FEPPA can detect BAT and newly formed beige fat under non-stimulated, thermoneutral conditions and that uptake after stimulation is linked to mitochondrial expression as opposed to activation. © 2019 The Authors | Source Title: | Molecular Metabolism | URI: | https://scholarbank.nus.edu.sg/handle/10635/210760 | ISSN: | 22128778 | DOI: | 10.1016/j.molmet.2019.05.003 | Rights: | Attribution-NonCommercial-NoDerivatives 4.0 International |
Appears in Collections: | Elements Staff Publications |
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