Kojyl cinnamate esters are peroxisome proliferator-activated receptor α/γ dual agonists

被引:14
|
作者
Kim, Sae On [1 ,2 ]
Han, Yujia [1 ,2 ]
Ahn, Sungjin [1 ,2 ]
An, Seungchan [1 ,2 ]
Shin, Jeayoung C. [1 ,2 ]
Choi, Hyunjung [3 ]
Kim, Hyoung-June [3 ]
Park, Nok Hyun [3 ]
Kim, Yong-Jin [3 ]
Jin, Sun Hee [1 ,2 ]
Rho, Ho Sik [4 ]
Noh, Minsoo [1 ,2 ]
机构
[1] Seoul Natl Univ, Coll Pharm, 1 Gwanak Ro, Seoul 08826, South Korea
[2] Seoul Natl Univ, Nat Prod Res Inst, 1 Gwanak Ro, Seoul 08826, South Korea
[3] AmorePacif Corp R&D Ctr, Yongin 17074, Gyeounggi Do, South Korea
[4] Univ Suwon, Dept Chem & Mat Engn, Gyeounggi Do 18323, South Korea
基金
新加坡国家研究基金会;
关键词
Kojyl cinnamate ester derivatives; Human adipose tissue-derived mesenchymal stem cells; Adiponectin; Peroxisome proliferator-activated receptor dual modulators; MESENCHYMAL STEM-CELLS; PPAR-GAMMA; ADIPOCYTE DIFFERENTIATION; ADIPONECTIN PRODUCTION; PERMEABILITY BARRIER; LIPID-SYNTHESIS; ADIPOGENESIS; METABOLISM; MECHANISM; MODEL;
D O I
10.1016/j.bmc.2018.10.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Adiponectin is an adipocytokine with insulin-sensitizing, anti-inflammatory, anti-atherosclerotic, and anti-aging properties. Compounds with the ability to promote adiponectin secretion are of interest for the development of anti-aging drugs to improve skin-aging phenotypes. In the phenotypic assay to measure adiponectin secretion during adipogenesis in human adipose tissue-derived mesenchymal stem cells (hAT-MSCs), kojyl cinnamate ester derivatives increased adiponectin secretion. A target identification study showed that the kojyl cinnamate ester derivatives competitively bound to peroxisome proliferator-activated receptor alpha/gamma (PPAR alpha/gamma). The upregulation of adiponectin production induced by kojyl cinnamate ester derivatives was significantly correlated with PPAR alpha and PPAR gamma binding activities. Kojyl cinnamate ester derivatives significantly increased the transcription of genes encoding cholesterol and fatty acid synthesizing enzymes in hAT-MSCs. Notably, the kojyl cinnamate esters upregulated the gene transcription of lipid metabolic enzymes in human epidermal keratinocytes, which are important in the integrity of skin permeability barrier. In addition, the kojyl cinnamate esters that function as PPAR alpha/gamma dual modulators inhibited ultraviolet B irradiation-induced inflammation in human epidermal keratinocytes. Therefore, kojyl cinnamate ester derivatives are a novel class of PPAR alpha/gamma dual agonists with the potential to improve skin-aging phenotypes.
引用
收藏
页码:5654 / 5663
页数:10
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