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Brown adipose tissue (BAT) is an important energy metabolic organ that is highly implicated in obesity, type 2 diabetes, and atherosclerosis. Aging is one of the most important determinants of BAT activity. In this study, we used  18 F-FDG PET/CT imaging to assess BAT aging in Lmna −/−  mice. The maximum standardized uptake value (SUV Max ) of the BAT was measured, and the target/nontarget (T/NT) values of BAT were calculated. The transcription and the protein expression levels of the uncoupling protein 1 (UCP1), beta3-adrenergic receptor ( β 3-AR), and the PR domain-containing 16 (PRDM16) were measured by quantitative real-time polymerase chain reaction (RT-PCR) and Western blotting or immunohistochemical analysis. Apoptosis and cell senescence rates in the BAT of WT and Lmna −/−  mice were determined by terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) and by CDKN2A/p16INK4a immunohistochemical staining, respectively. At 14 weeks of age, the BAT SUV Max  and the expression levels of UCP1,  β 3-AR, and PRDM16 in Lmna −/−  mice were significantly reduced relative to WT mice. At the same time, the number of p16INK4a and TUNEL positively stained cells (%) increased in Lmna −/−  mice. Collectively, our results indicate that the aging characteristics and the aging regulatory mechanism in the BAT of Lmna −/−  mice can mimic the normal BAT aging process.

Assessment of the Aging of the Brown Adipose Tissue by 18F-FDG PET/CT Imaging in the Progeria Mouse Model Lmna−/−

Assessment of the Aging of the Brown Adipose Tissue by ¹⁸F-FDG PET/CT Imaging in the Progeria Mouse Model Lmna^−/−