Cryptotanshinone, a compound of Salvia miltiorrhiza inhibits pre-adipocytes differentiation by regulation of adipogenesis-related genes expression via STAT3 signaling

被引:43
作者
Rahman, Naimur [1 ]
Jeon, Miso [1 ]
Song, Ho-Yeon [1 ]
Kim, Yong-Sik [1 ,2 ]
机构
[1] Soonchunhyang Univ, Coll Med, Dept Microbiol, Cheonan, South Korea
[2] Soonchunhyang Univ, Coll Med, Inst Tissue Engn, Cheonan, South Korea
基金
新加坡国家研究基金会;
关键词
Crypiolanshinoi; Adipogenesis; C/EBP beta; PPAR gamma; STAT3; DIET-INDUCED OBESITY; PPAR-GAMMA; RETINOIC ACID; PROTEIN; CELLS; CONVERSION; ALPHA;
D O I
10.1016/j.phymed.2015.12.004
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Background: Cryptotanshinone (CT), a major tanshinone found in Salvia rrtitliorrhiza Bunge (Lcniacecie), has various pharmacological effects such as antitumor, anti-inflammatory, and antioxidant properties. Despite its well-documented benefits in a wide range of diseases, the effect of CT on adipocyte differentiation has not been well characterized. Purpose: The present study was designed to determine the in vitro anti-adipogenic effect and underlying molecular mechanisms of CT using 3T3-L1 murine pre-adipocytes. Methods: We measured the levels of intracellular triglyceride accumulation and mRNA and protein expression of key adipogenic transcription factors and their target genes. Results: Treatment with CT drastically reduced lipid accumulation in a dose-and time-dependent manner. Molecular assays showed that CT effectively suppressed the expression of C/EBP beta, C/EBP alpha, and PPAR gamma and of theft target adipocyte-specific genes aP2, adiponectin, and GUIT4 but activated the expression of anti-adipogenic genes such as GATA2, CH0P10, and TNT-alpha. CT treatment also inhibited the phosphorylation of STAT3 in the early phase of adipogenesis. A small-interfering-RNA-mediated knockdown of STAT3 potentiated the anti-adipogenic effect of CT. Conclusion: Taken together, the results suggest that CT may be a good anti-adipogenic candidate because it regulates STAT3 during early adipogenesis. (C) 2015 Elsevier GmbH. All rights reserved.
引用
收藏
页码:58 / 67
页数:10
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