Inhibitory Effect of Vitamin U (S-Methylmethionine Sulfonium Chloride) on Differentiation in 3T3-L1 Pre-adipocyte Cell Lines.
	    		
		   		
		   			
		   		
	    	
    	- Author:
	        		
		        		
		        		
			        		Na Young LEE
			        		
			        		
			        		
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			        		Kui Young PARK
			        		
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			        		Hye Jung MIN
			        		
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			        		Kye Yong SONG
			        		
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			        		Yun Young LIM
			        		
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			        		Juhee PARK
			        		
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			        		Beom Joon KIM
			        		
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			        		Myeung Nam KIM
			        		
			        		
		        		
		        		
		        		
			        		
			        		Author Information
			        		
 - Publication Type:Original Article
 - Keywords: Adipocyte differentiation; S-methylmethionine sulfonium chloride; Vitamin U
 - MeSH: 1-Methyl-3-isobutylxanthine; Adipocytes; AMP-Activated Protein Kinases; Cell Line; Complement Factor D; Digestive System; Down-Regulation; Fatty Acid Synthetase Complex; Flowers; Glycerolphosphate Dehydrogenase; Insulin; Lipoproteins; Triglycerides; Ulcer; Up-Regulation; Vitamin U; Vitamins
 - From:Annals of Dermatology 2012;24(1):39-44
 - CountryRepublic of Korea
 - Language:English
 - Abstract: BACKGROUND: S-methylmethionine sulfonium chloride was originally called vitamin U because of its inhibition of ulceration in the digestive system. Vitamin U is ubiquitously expressed in the tissues of flowering plants, and while there have been reports on its hypolipidemic effect, its precise function remains unknown. OBJECTIVE: This study was designed to evaluate the anti-obesity effect of vitamin U in 3T3-L1 pre-adipocyte cell lines. METHODS: We cultured the pre-adipocyte cell line 3T3L1 to overconfluency and then added fat differentiation-inducing media (dexamethasone, IBMX [isobutylmethylxanthine], insulin, indomethacin) and different concentrations (10, 50, 70, 90, 100 mM) of vitamin U. Then, we evaluated changes in the levels of triglycerides (TGs), glycerol-3-phosphate dehydrogenase (G3PDH), AMP-activated protein kinase (AMPK), adipocyte-specific markers (peroxisome proliferator-activated receptor gamma [PPAR-gamma], CCAAT/enhancer-binding protein alpha [C/EBP-alpha], adipocyte differentiation and determination factor 1 [ADD-1], adipsin, fatty acid synthase, lipoprotein lipase) and apoptosis-related signals (Bcl-2, Bax). RESULTS: There was a gradual decrease in the level of TGs, C/EBP-alpha, PPAR-gamma, adipsin, ADD-1 and GPDH activity with increasing concentrations of vitamin U. In contrast, we observed a significant increase in AMPK activity with increasing levels of vitamin U. The decrease in bcl-2 and increase in Bax observed with increasing concentrations of vitamin U in the media were not statistically significant. CONCLUSION: This study suggests that vitamin U inhibits adipocyte differentiation via down-regulation of adipogenic factors and up-regulation of AMPK activity.
 
            