The combined effect of metformin and mirabegron on diet-induced obesity.
Xin-Yuan ZhaoYing LiuXuan ZhangBen-Chi ZhaoGeorge BurleyZhi-Can YangYi LuoAn-Qi LiRuo-Xin ZhangZhi-Ying LiuYan-Chuan ShiG Gregory NeelyPublished in: MedComm (2023)
Anti-obesity medications act by suppressing energy intake (EI), promoting energy expenditure (EE), or both. Metformin (Met) and mirabegron (Mir) cause weight loss by targeting EI and EE, respectively. However, anti-obesity effects during concurrent use of both have yet to be explored. In this study, we investigated the anti-obesity effects, metabolic benefits, and underlying mechanisms of Met/Mir combination therapy in two clinically relevant contexts: the prevention model and the treatment model. In the prevention model, Met/Mir caused further 12% and 14% reductions in body weight (BW) gain induced by a high-fat diet compared to Met or Mir alone, respectively. In the treatment model, Met/Mir additively promoted 17% BW loss in diet-induced obese mice, which was 13% and 6% greater than Met and Mir alone, respectively. Additionally, Met/Mir improved glucose tolerance and insulin sensitivity. These benefits of Met/Mir were associated with increased EE, activated brown adipose tissue thermogenesis, and white adipose tissue browning. Significantly, Met/Mir did not cause cardiovascular dysfunction in either model. Together, the combination of Met and Mir could be a promising approach for the prevention and treatment of obesity by targeting both EI and EE simultaneously.
Keyphrases
- cell proliferation
- long non coding rna
- adipose tissue
- weight loss
- insulin resistance
- long noncoding rna
- high fat diet
- tyrosine kinase
- metabolic syndrome
- type diabetes
- high fat diet induced
- weight gain
- body weight
- squamous cell carcinoma
- skeletal muscle
- physical activity
- radiation therapy
- roux en y gastric bypass
- mass spectrometry
- rectal cancer
- glycemic control