Literature DB >> 28543963

Ageing is associated with brown adipose tissue remodelling and loss of white fat browning in female C57BL/6 mice.

Leidyanne Ferreira Gonçalves1, Thaissa Queiroz Machado1, Camila Castro-Pinheiro1, Nathalia Guimaraes de Souza2, Karen Jesus Oliveira2, Caroline Fernandes-Santos1.   

Abstract

Fat storage changes throughout life and affects body metabolism. Ageing impact on brown (BAT) and white adipose tissue (WAT) deserves attention, especially in females, because they are less prone to age-induced weight gain. While in male mice the impact of ageing on adipose tissue remodelling is well characterized, the effects in female mice remain largely unclear. Thus, we investigated BAT and WAT remodelling during ageing in female C57BL/6 mice. At 3 months, body weight was 24 ± 0.3 g (mean±SD), and it increased from 6 to 9 months of age (+20%, P < 0.0001). Oral glucose tolerance test showed no disturbance of glucose metabolism. All WAT depots became heavier, and white adipocytes hypertrophied. The subcutaneous and visceral WAT had clusters of beige cells in younger mice, but they were progressively lost by ageing, indicating loss of WAT browning. Older mice had hypertrophied classic brown adipocytes that had larger cytoplasmic lipid droplets than younger mice. Pearson's correlation showed that WAT mass has a weak correlate with BAT mass, although white adipocyte diameter has a strong correlation with classic brown adipocyte size. In conclusion, our results indicate that female C57BL/6 mice have a progressive age-dependent loss of subcutaneous and visceral WAT browning, and this process runs in parallel with BAT morphological changes towards a fat storer phenotype, independent of cycling or disturbances in glucose metabolism.
© 2017 The Authors. International Journal of Experimental Pathology © 2017 International Journal of Experimental Pathology.

Entities:  

Keywords:  ageing; female; metabolism; mice; obesity

Mesh:

Year:  2017        PMID: 28543963      PMCID: PMC5485357          DOI: 10.1111/iep.12228

Source DB:  PubMed          Journal:  Int J Exp Pathol        ISSN: 0959-9673            Impact factor:   1.925


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