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Updated: Jun 12, 2025

Measurement of Basal and Forskolin-stimulated Lipolysis in Inguinal Adipose Fat Pads
Published on: July 21, 2017
Rifampicin prevents diet-induced obesity through Sirt6-dependent lipolysis, adipocyte browning and lipogenesis
Yang Xu1, Lei Cao1, Xiaoyuan Guo1
1State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.
Abstract:
Rifampicin (RFP) is a semi-synthetic macrocyclic broad-spectrum antibiotic known for its ability to inhibit bacterial proliferation. However, its potential role of obesity treatment has not been explored. We unveil a novel function of rifampicin using 3T3-L1 adipocytes and high-fat diet (HFD)-fed mice. Rifampicin upregulates Sirt6 expression both in vitro and in vivo. Furthermore, rifampicin inhibits 3T3-L1 preadipocyte differentiation and lipid accumulation by suppressing lipogenesis and enhancing lipolysis. Oral administration of rifampicin effectively inhibits body weight gain in HFD-fed mice. Mechanistically, rifampicin significantly suppresses lipogenesis, and enhances lipolysis, energy expenditure and the white adipose tissue browning-related pathway in the inguinal white adipose tissue (iWAT) of HFD-fed mice. Importantly, deletion of adipose Sirt6 abolishes the effects of rifampicin on HFD-induced weight gain and obesity in mice. Our data collectively reveal that rifampicin alleviates diet-induced obesity by inducing Sirt6. These findings may support a novel approach to treat obesity.
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