Publication: Regulation of adipocyte differentiation and metabolism by lansoprazole
Issued Date
2019-12-15
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ISSN
18790631
00243205
00243205
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2-s2.0-85073929140
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Mahidol University
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SCOPUS
Bibliographic Citation
Life Sciences. Vol.239, (2019)
Suggested Citation
Ameena Benchamana, Hiroyuki Mori, Ormond A. MacDougald, Sunhapas Soodvilai Regulation of adipocyte differentiation and metabolism by lansoprazole. Life Sciences. Vol.239, (2019). doi:10.1016/j.lfs.2019.116897 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/49995
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Title
Regulation of adipocyte differentiation and metabolism by lansoprazole
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Abstract
© 2019 Aims: Lansoprazole (LPZ) is one of the most commonly prescribed drugs for treatment of acid-related diseases, and it is increasingly recognized for its potential application as an anti-diabetic therapy. Although LPZ target tissues remain poorly understood, possible sites of action include adipose tissue. In this study, we assessed effects of LPZ on adipocyte differentiation and function by using 3T3-L1 preadipocytes and HFD-induced obesity mice as an in vitro and in vivo model, respectively. Main methods: Oil red O staining and intracellular triacylglycerol content were used to determine lipid accumulation. Glucose uptake was performed to measure mature adipocyte function. Expression of adipocyte genes was determined by qRT-PCR and immunoblotting. Key findings: LPZ has dual effects on differentiation of 3T3-L1 cells. At low concentrations, LPZ enhanced adipocyte differentiation via induction of PPARγ and C/EBPα, two master adipogenic transcription factors, as well as lipogenic proteins, ACC1 and FASN. Increasing of adipocyte number subsequently increased basal and insulin-stimulated glucose uptake, and expression of Glut4 mRNA. Conversely, high concentrations of LPZ strongly inhibited differentiation and expression of PPARγ and C/EBPα, and maintained expression of preadipocytes markers, β-catenin and Pref-1. Inhibition of adipogenesis by LPZ reduced mature adipocyte number, Glut4 mRNA expression and insulin-stimulated glucose uptake. In addition, treatment with LPZ at 200 mg/kg significantly reduced body weight gain and total fat mass in HFD-induced obese mice. Significance: These results indicate that effects of LPZ on adipocyte differentiation are dependent on concentration and are correlated with PPARγ and C/EBPα.