Abstract

Brown adipose tissue (BAT), a uniquely thermogenic tissue that plays an important role in metabolism and energy expenditure, has recently become a revived target in the fight against metabolic diseases, such as obesity, diabetes, and non-alcoholic fatty liver disease (NAFLD). Different from white adipose tissue (WAT), the brown adipocytes have distinctive features including multilocular lipid droplets, a large number of mitochondria, and a high expression of uncoupling protein-1 (UCP-1), as well as abundant capillarity. These histologic characteristics provide an opportunity to differentiate BAT from WAT using imaging modalities, such as PET/CT, SPECT/CT, MRI, NIRF and Ultrasound. However, most of the reported imaging methods were BAT activation dependent, and the imaging signals could be affected by many factors, including environmental temperatures and the states of the sympathetic nervous system. Accurate BAT mass detection methods that are independent of temperature and hormone levels have the capacity to track the development and changes of BAT throughout the lifetime of mammals, and such methods could be very useful for the investigation of potential BAT-related therapies. In this review, we focus on molecular imaging modalities that can detect and quantify BAT mass. In addition, their detection mechanism and limitations will be discussed as well.

Highlights

  • Brown adipose tissue (BAT) is a specialized tissue for thermogenesis, and its function in mammals is to dissipate large amounts of chemical/food energy as heat, maintaining an energy balance of the whole body [1,2,3]

  • positron emission tomography (PET) tracers targeting BAT were designed according to the unique characteristics of BAT, including dense mitochondria packing, high metabolic activity, and high expression of unique proteins, such as uncoupling protein-1 (UCP-1) and translocator protein (TSPO)

  • Two near-infrared spectroscopy (NIRS) techniques were commonly used for BAT properties monitoring: near-infrared time resolved spectroscopy (NIRTRS) that targets the oxygenated and deoxygenated hemoglobin and near-infrared continuous wavelength spectroscopy (NIRcws) that measures the relative oxygenation changes in the tissue [110]

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Summary

Introduction

BAT is a specialized tissue for thermogenesis, and its function in mammals is to dissipate large amounts of chemical/food energy as heat, maintaining an energy balance of the whole body [1,2,3]. The most distinct characteristics of BAT include a large number of mitochondria, abundant uncoupling protein-1 (UCP-1) expression, numerous small oil droplets in a single cell, as well as significant vascularization of BAT tissue [1,38,39,40,41]. These characteristics strongly indicate that BAT plays an important role in metabolism and energy expenditure, and regulating BAT mass and activation represents a very attractive approach for obesity and diabetes treatment. BAT mass is the actual weight of the tissue that is consistent with and without stimulations, such as cold exposure and beta-agonist treatment, while BAT activation, reflecting

18 F-FMPEP-d2 18 F-F-DPA 18 F-F-FEPPA 18 F-F-PBR28 64 Cu-Dis
Limitations
11 C-acetate
Imaging Modalities for BAT Detection
Other Imaging Modalities for BAT Imaging
Findings
Discussion and Future
Conclusions
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