Background: In vivo imaging of glucose analogue 2-deoxy-2-[F]fluoro-D-glucose ([F]FDG) via positron emission tomography (PET) is the current gold standard to visualize and assess brown adipose tissue (BAT) activity. However, glucose metabolism is only a part of the metabolic activity of BAT. [F]FDG-PET has been shown in clinical trials to often fail to visualize BAT under insulin-resistant conditions associated with aging and weight gain. We employed a novel developed triglyceride-based tracer to visualize BATs metabolic activity under different temperature conditions as well as under diabetic and obese conditions in preclinical models.
Results: [F]BDP-TG-chylomicron-like particles visualized BAT in control, streptozocin-induced diabetes and obese mice. Increased BAT tracer uptake was found in control mice acutely exposed to cold but not in cold-acclimated animals. Diabetes did not remove BAT tracer uptake, but did limit BAT tracer uptake to levels of control mice housed at 21 °C. In obese animals, BAT tracer uptake was significantly reduced, although the stimulating effect of cold exposure could still be noted.
Conclusion: BAT was visualized in control, diabetic and obese conditions. Streptozocin-induced diabetes, but not obesity, inhibited the stimulatory effect of cold exposure.
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http://dx.doi.org/10.1186/s13550-020-00701-6 | DOI Listing |
J Contam Hydrol
May 2024
Université de Poitiers/CNRS, UMR 7285 IC2MP, Equipe HydrASA, 5 rue Albert Turpain, Bât. B8, TSA - 51106, 86073 Poitiers cedex 9, France.
Molecules
February 2024
Université Paris-Saclay, CNRS, BioCIS, Bat. Henri Moissan, 17, Av. des Sciences, 91400 Orsay, France.
Physiology (Bethesda)
March 2024
Department of Medicine, Division of Endocrinology, Centre de Recherche du Centre Hospitalier Universitaire de Sherbrooke, Université de Sherbrooke, Sherbrooke, Quebec, Canada.
White adipose tissue and brown adipose tissue (WAT and BAT) regulate fatty acid metabolism and control lipid fluxes to other organs. Dysfunction of these key metabolic processes contributes to organ insulin resistance and inflammation leading to chronic diseases such as type 2 diabetes, metabolic dysfunction-associated steatohepatitis, and cardiovascular diseases. Metabolic tracers combined with molecular imaging methods are powerful tools for the investigation of these pathogenic mechanisms.
View Article and Find Full Text PDFExpert Rev Med Devices
November 2023
Nuclear Medicine Unit, St. Salvatore Hospital, L'Aquila, Italy.
Introduction: This review provides an update of 18 F-fluorodeoxyglucose ([F] FDG) for Brown adipose tissue (BAT) activity quantification, whose role is not completely understood.
Areas Covered: We conducted an unstructured search of the literature for any studies employing the [F] FDG PET in BAT assessment. We explored BAT quantification both in healthy individuals and in different pathologies, after cold exposure and as a metabolic biomarker.
Am J Physiol Heart Circ Physiol
January 2024
Department of Chemical Physiology and Biochemistry, Oregon Health and Science University, Portland, Oregon, United States.
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