Analysis of transcriptomic, lipidomic and phospho-kinase profiles reveals the effects of chlorogenic acid on 3T3-L1 preadipocytes differentiation
[Display omitted] •CGA treatment during differentiation resulted in transcriptome changes in 3 T3-L1 cells.•CGA treatment during differentiation altered cellular lipid profile in 3 T3-L1 cells.•CGA treatment during differentiation inhibited adipogenesis-related kinases in 3 T3-L1 cells. Chlorogenic...
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Published in | Journal of functional foods Vol. 110; p. 105828 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier Ltd
01.11.2023
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | [Display omitted]
•CGA treatment during differentiation resulted in transcriptome changes in 3 T3-L1 cells.•CGA treatment during differentiation altered cellular lipid profile in 3 T3-L1 cells.•CGA treatment during differentiation inhibited adipogenesis-related kinases in 3 T3-L1 cells.
Chlorogenic acid has been widely reported to profoundly influence preadipocyte differentiation but without consensus being achieved. In the current study, 3 T3-L1 preadipocytes were differentiated using adipogenic cocktail with or without chlorogenic acid. The influences of chlorogenic acid on the mRNA, lipid and phospho-kinase profiles were evaluated using transcriptomic analysis, lipidomic analysis and phospho-kinase array assay. The obtained results showed that chlorogenic acid treatment during 3T3-L1 cells differentiation altered a series of genes transcription, resulted in obvious changes in the contents of various lipids, and inhibited phosphorylation of several adipogenesis-related kinases. Overall, the observed changes in transcriptomic, lipidomic and phospho-kinase profiles in the current study favor the findings that chlorogenic acid may inhibit the differentiation of 3T3-L1 preadipocytes. In conclusion, the findings from this study highlighted the therapeutic potential of chlorogenic acid for the treatment of obesity. |
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ISSN: | 1756-4646 2214-9414 |
DOI: | 10.1016/j.jff.2023.105828 |