Tamarixetin Abrogates Adipogenesis Through Inhibiting p300/CBP-Associated Factor Acetyltransferase Activity in 3T3-L1 Preadipocyte Cells.

Tamarixetin (TX) is an O-methylated flavonoid naturally derived from quercetin. TX has bioactive properties; however, whether it shows antilipogenic activity remains unknown. Therefore, in the present study, we aimed to determine the antilipogenic effects of TX using 3T3-L1 adipocytes. The 3T3-L1 ad...

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Publicado en:Journal of Medicinal Food Vol. 25; no. 3; pp. 272 - 281
Autores principales: Kim, Hyo-Jin, Lee, Jangho, Chung, Min-Yu, Park, Soo Hyun, Park, Jae Ho, Choi, Hyo-Kyoung, Hwang, Jin-Taek
Formato: pictorial research tables/charts Journal Article
Publicado: Mary Ann Liebert, Inc. Mar2022
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Mar2022
      vid: 25
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      pub: Mary Ann Liebert, Inc.
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        10.1089/jmf.2021.K.0126
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        atl: Tamarixetin Abrogates Adipogenesis Through Inhibiting p300/CBP-Associated Factor Acetyltransferase Activity in 3T3-L1 Preadipocyte Cells.
      aug:
        au:
          Kim, Hyo-Jin
          Lee, Jangho
          Chung, Min-Yu
          Park, Soo Hyun
          Park, Jae Ho
          Choi, Hyo-Kyoung
          Hwang, Jin-Taek
        affil: Korea Food Research Institute, Jeollabuk-do, Korea.
      sug:
        subj:
          Antilipemic Agents Pharmacodynamics
          Quercetin Pharmacodynamics
          Adipocytes Drug Effects
          Adipose Tissue Drug Effects
          Transferases Drug Effects
          Animal Studies
          Mice
          Lipids Drug Effects
          RNA, Messenger
          Gene Expression Drug Effects
      ab: Tamarixetin (TX) is an O-methylated flavonoid naturally derived from quercetin. TX has bioactive properties; however, whether it shows antilipogenic activity remains unknown. Therefore, in the present study, we aimed to determine the antilipogenic effects of TX using 3T3-L1 adipocytes. The 3T3-L1 adipocytes were cultured in a differentiation medium with or without TX. Lipid accumulation was diminished and the mRNA expression of lipogenesis-related genes was decreased following TX treatment. We found that TX exhibited antilipogenic effects by inhibiting the expression of p300/CBP-associated factor (pCAF), a histone acetyltransferase, as confirmed by pCAF knockdown. Furthermore, TX inhibited both pCAF expression and its activity, thereby reducing the total acetylation level of nonhistone and histone proteins. Finally, TX decreased the expression of CCAAT/enhancer-binding protein alpha and beta (CEBPα and CEBPβ), and peroxisome proliferator-activated receptor γ along with pCAF expression during adipogenesis of 3T3-L1 cells in a time-dependent manner. Collectively, our findings suggest that TX is a potent antilipogenic agent derived from natural products and may be used as a pCAF inhibitor.
      pubtype: Academic Journal
      doctype:
        pictorial
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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