scholarly journals The beneficial effects of brown adipose tissue transplantation

2019 ◽  
Vol 68 ◽  
pp. 74-81 ◽  
Author(s):  
Joseph D. White ◽  
Revati S. Dewal ◽  
Kristin I. Stanford
2018 ◽  
Vol 314 (2) ◽  
pp. E131-E138 ◽  
Author(s):  
Hidechika Morimoto ◽  
Jun Mori ◽  
Hisakazu Nakajima ◽  
Yasuhiro Kawabe ◽  
Yusuke Tsuma ◽  
...  

The renin-angiotensin system is a key regulator of metabolism with beneficial effects of the angiotensin 1–7 (Ang 1–7) peptide. We hypothesized that the antiobesity effect of Ang 1–7 was related to the stimulation of brown adipose tissue (BAT). We administered Ang 1–7 (0.54 mg kg−1 day−1) for 28 days via implanted micro-osmotic pumps to mice with high-fat diet (HFD)-induced obesity. Ang 1–7 treatment reduced body weight, upregulated thermogenesis, and ameliorated impaired glucose homeostasis without affecting food consumption. Furthermore, Ang 1–7 treatment enlarged BAT and the increased expression of UCP1, PRDM16, and prohibitin. Alterations in PRDM16 expression correlated with increased AMPK and phosphorylation of mTOR. Ang 1–7 treatment elevated thermogenesis in subcutaneous white adipose tissue without altering UCP1 expression. These changes occurred in the context of decreased lipid accumulation in BAT from HFD-fed mice, preserved insulin signaling concomitant with phosphorylation of hormone-sensitive lipase and decreased expression of perilipin. These data suggest that Ang 1–7 induces brown adipocyte differentiation leading to upregulation of thermogenesis and improved metabolic profile in diet-induced obesity. Enhancing Ang 1–7 action represents a promising therapy to increase BAT and to reduce the metabolic complications associated with diet-induced obesity.


Endocrinology ◽  
2015 ◽  
Vol 156 (7) ◽  
pp. 2461-2469 ◽  
Author(s):  
Xiaomeng Liu ◽  
Siping Wang ◽  
Yilin You ◽  
Minghui Meng ◽  
Zongji Zheng ◽  
...  

2018 ◽  
Vol 155 ◽  
pp. 346-355 ◽  
Author(s):  
M. Carmen Soler-Vázquez ◽  
Paula Mera ◽  
Sebastián Zagmutt ◽  
Dolors Serra ◽  
Laura Herrero

2020 ◽  
Vol 45 (1) ◽  
pp. 109-121 ◽  
Author(s):  
Moloud Payab ◽  
Mina Abedi ◽  
Najmeh Foroughi Heravani ◽  
Mahdieh Hadavandkhani ◽  
Maryam Arabi ◽  
...  

Gut ◽  
2019 ◽  
Vol 69 (7) ◽  
pp. 1239-1247 ◽  
Author(s):  
Lin-Hu Quan ◽  
Chuanhai Zhang ◽  
Meng Dong ◽  
Jun Jiang ◽  
Hongde Xu ◽  
...  

ObjectiveDietary fibre has beneficial effects on energy metabolism, and the majority of studies have focused on short-chain fatty acids produced by gut microbiota. Ginseng has been reported to aid in body weight management, however, its mechanism of action is not yet clear. In this study, we focused on the potential modulating effect of ginseng on gut microbiota, aiming to identify specific strains and their metabolites, especially long-chain fatty acids (LCFA), which mediate the anti-obesity effects of ginseng.DesignDb/db mice were gavaged with ginseng extract (GE) and the effects of GE on gut microbiota were evaluated using 16S rDNA-based high throughput sequencing. To confirm the candidate fatty acids, untargeted metabolomics analyses of the serum and medium samples were performed.ResultsWe demonstrated that GE can induce Enterococcus faecalis, which can produce an unsaturated LCFA, myristoleic acid (MA). Our results indicate that E. faecalis and its metabolite MA can reduce adiposity by brown adipose tissue (BAT) activation and beige fat formation. In addition, the gene of E. faecalis encoding Acyl-CoA thioesterases (ACOTs) exhibited the biosynthetic potential to synthesise MA, as knockdown (KD) of the ACOT gene by CRISPR-dCas9 significantly reduced MA production. Furthermore, exogenous treatment with KD E. faecalis could not reproduce the beneficial effects of wild type E. faecalis, which work by augmenting the circulating MA levels.ConclusionsOur results demonstrated that the gut microbiota-LCFA-BAT axis plays an important role in host metabolism, which may provide a strategic advantage for the next generation of anti-obesity drug development.


Cell Research ◽  
2013 ◽  
Vol 23 (6) ◽  
pp. 851-854 ◽  
Author(s):  
Xiaomeng Liu ◽  
Zongji Zheng ◽  
Xiaoming Zhu ◽  
Minghui Meng ◽  
Lan Li ◽  
...  

Cytotherapy ◽  
2020 ◽  
Vol 22 (10) ◽  
pp. 521-528 ◽  
Author(s):  
Kang-Yun Lu ◽  
Kingsley Theras Primus Dass ◽  
Shinn-Zong Lin ◽  
Horng-Jyh Harn ◽  
Shih-Ping Liu

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