Aspartame downregulates 3T3-L1 differentiation.

Abstract

Aspartame is an artificial sweetener used as an alternate for sugar in several foods and beverages. Since aspartame is 200 times sweeter than traditional sugar, it can give the same level of sweetness with less substance, which leads to lower-calorie food intake. There are reports that consumption of aspartame-containing products can help obese people lose weight. However, the potential role of aspartame in obesity is not clear. The present study investigated whether aspartame suppresses 3T3-L1 differentiation, by downregulating phosphorylated peroxisome proliferator-activated receptor γ (p-PPARγ), peroxisome proliferator-activated receptor γ (PPARγ), fatty acid-binding protein 4 (FABP4), CCAAT/enhancer-binding protein α (C/EBPα), and sterol regulatory element-binding protein 1 (SREBP1), which are critical for adipogenesis. The 3T3-L1 adipocytes were cultured and differentiated for 6 d in the absence and presence of 10 μg/ml of aspartame. Aspartame reduced lipid accumulation in differentiated adipocytes as evidenced by Oil Red O staining. qRT-PCR analysis showed that the PPARγ, FABP4, and C/EBPα mRNA expression was significantly reduced in the aspartame-treated adipocytes. Western blot analysis showed that the induction of p-PPARγ, PPARγ, SREBP1, and adipsin was markedly reduced in the aspartame-treated adipocytes. Taken together, these data suggest that aspartame may be a potent substance to alter adipocyte differentiation and control obesity.

• Authors: Muthuraman Pandurangan, Jeongeun Park, Eunjung Kim
• Journal: In vitro cellular & developmental biology. Animal (In Vitro Cell Dev Biol Anim) Vol. 50 Issue 9 Pg. 851-7 (Oct 2014) ISSN: 1543-706X [Electronic] Germany
• PMID: 24961835 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• CCAAT-Enhancer-Binding Protein-alpha
• Fabp4 protein, mouse
• Fatty Acid-Binding Proteins
• PPAR gamma
• Sterol Regulatory Element Binding Protein 1
• Aspartame

Topics

• Adipocytes (drug effects)
• Adipogenesis (drug effects)
• Animals
• Aspartame (pharmacology)
• CCAAT-Enhancer-Binding Protein-alpha (metabolism)
• Cell Differentiation (drug effects)
• Fatty Acid-Binding Proteins (metabolism)
• Gene Expression Regulation (drug effects)
• Lipid Metabolism (drug effects)
• Mice
• NIH 3T3 Cells
• PPAR gamma (genetics)
• Sterol Regulatory Element Binding Protein 1 (metabolism)