Key result
Cold exposure upregulates Ucp1 expression ~729-fold in bat intra-abdominal white adipose tissue.
Why the study?
Animal models for beige fat induction are limited to rodents where subcutaneous WAT is more prone to browning than intra-abdominal WAT, which is the major source of obesity-related diseases in humans.
The great roundleaf bat may serve as a useful animal model for studying cold-induced browning of intra-abdominal white adipose tissue, which is relevant for obesity research.
Answers are grounded in this paper and cite their sources.
May position the great roundleaf bat as a model for intra-abdominal WAT browning; leaves open human translation for obesity.
BACKGROUND: Inducing beige fat from white adipose tissue (WAT) is considered to be a shortcut to weight loss and increasingly becoming a key area in research into treatments for obesity and related diseases. However, currently, animal models of beige fat are restricted to rodents, where subcutaneous adipose tissue (sWAT, benign WAT) is more liable to develop into the beige fat under specific activators than the intra-abdominal adipose tissue (aWAT, malignant WAT) that is the major source of obesity related diseases in humans. METHODS: Here we induced beige fat by cold exposure in two species of bats, the great roundleaf bat (Hipposideros armiger) and the rickett's big-footed bat (Myotis ricketti), and compared the molecular and morphological changes with those seen in the mouse. Expression of thermogenic genes (Ucp1 and Pgc1a) was measured by RT-qPCR and adipocyte morphology examined by HE staining at three adipose locations, sWAT, aWAT and iBAT (interscapular brown adipose tissue). RESULTS: Expression of Ucp1 and Pgc1a was significantly upregulated, by 729 and 23 fold, respectively, in aWAT of the great roundleaf bat after exposure to 10°C for 7 days. Adipocyte diameters of WATs became significantly reduced and the white adipocytes became brown-like in morphology. In mice, similar changes were found in the sWAT, but much lower amounts of changes in aWAT were seen. Interestingly, the rickett's big-footed bat did not show such a tendency in beige fat. CONCLUSIONS: The great roundleaf bat is potentially a good animal model for human aWAT browning research. Combined with rodent models, this model should be helpful for finding therapies for reducing harmful aWAT in humans.
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Wang et al. (2014) studied Obesity (Animal Model for Beige Fat) (n=45). Cold exposure vs. 30°C was evaluated on Ucp1 expression in intra-abdominal white adipose tissue (aWAT) (729-fold increase, p=<0.01). Cold exposure at 10°C for 7 days significantly upregulated Ucp1 expression by 729-fold in the intra-abdominal white adipose tissue of the great roundleaf bat compared to 30°C controls.
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