scholarly journals Inhibitory effects of Pericarpium zanthoxyli extract on adipocyte differentiation

2014 ◽  
Vol 33 (5) ◽  
pp. 1140-1146 ◽  
Author(s):  
HA-RIM KIM ◽  
JEONG-MI KIM ◽  
MI-SEONG KIM ◽  
JIN-KI HWANG ◽  
SEI-HOON YANG ◽  
...  
2008 ◽  
Vol 11 (5) ◽  
pp. 557-562 ◽  
Author(s):  
Mi-Ja Kim ◽  
Un-Jae Chang ◽  
Jin-Sil Lee

2021 ◽  
Vol 11 (4) ◽  
pp. 1725
Author(s):  
Hee-Do Hong ◽  
Sun-Il Choi ◽  
Ok-Hwan Lee ◽  
Young-Cheul Kim

Although ginsenosides Rb1 and Rg3 have been identified as the significant ginsenosides found in red ginseng that confer anti-diabetic actions, it is unclear whether insulin-sensitizing effects are mediated by the individual compounds or by their combination. To determine the effect of ginsenosides Rb1 and Rg3 on adipocyte differentiation, 3T3-L1 preadipocytes were induced to differentiate the standard hormonal inducers in the absence or presence of ginsenosides Rb1 or Rg3. Additionally, we determined the effects of Rb1, Rg3, or their combination on the expression of genes related to adipocyte differentiation, adipogenic transcription factors, and the insulin signaling pathway in 3T3-L1 cells using semi-quantitative RT-PCR. Rb1 significantly increased the expression of CEBPα, PPARγ, and aP2 mRNAs. However, Rg3 exerted its maximal stimulatory effect on these genes at 1 μM concentration, while a high concentration (50 μM) showed inhibitory effects. Similarly, treatment with Rb1 and Rg3 (1 μM) increased the expression of IRS-1, Akt, PI3K, GLUT4, and adiponectin. Importantly, co-treatment of Rb1 and Rg3 (9:1) induced the maximal expression levels of these mRNAs. Our data indicate that the anti-diabetic activity of red ginseng is, in part, mediated by synergistic actions of Rb1 and Rg3, further supporting the significance of minor Rg3.


2010 ◽  
Vol 73 (2) ◽  
pp. 172-176 ◽  
Author(s):  
IkSoo Lee ◽  
JungJu Seo ◽  
JinPyo Kim ◽  
HongJin Kim ◽  
UiJung Youn ◽  
...  

2014 ◽  
Vol 24 (5) ◽  
pp. 476-484 ◽  
Author(s):  
Yun-Hee Park ◽  
Jun-Hyeok Choi ◽  
Key Whang ◽  
Syng-Ook Lee ◽  
Seun-Ah Yang ◽  
...  

1997 ◽  
Vol 17 (2) ◽  
pp. 977-988 ◽  
Author(s):  
C M Smas ◽  
L Chen ◽  
H S Sul

pref-1 is an epidermal growth factor-like repeat protein present on the surface of preadipocytes that functions in the maintenance of the preadipose state. pref-1 expression is completely abolished during 3T3-L1 adipocyte differentiation. Bypassing this downregulation by constitutive expression of full-length transmembrane pref-1 in preadipocytes drastically inhibits differentiation. For the first time, we show processing of cell-associated pref-1 to generate both a soluble pref-1 protein of approximately 50 kDa that corresponds to the ectodomain and also smaller products of 24 to 25 kDa and 31 kDa. Furthermore, while all four of the alternately spliced forms of pref-1 produce cell-associated protein, only the two largest of the four alternately spliced isoforms undergo cleavage in the juxtamembrane region to release the soluble 50-kDa ectodomain. We demonstrate that addition of Escherichia coli-expressed pref-1 ectodomain to 3T3-L1 preadipocytes blocks differentiation, thus overriding the adipogenic actions of dexamethasone and methylisobutylxanthine. The inhibitory effects of the pref-1 ectodomain are blocked by preincubation of the protein with pref-1 antibody. That the ectodomain alone is sufficient for inhibition demonstrates that transmembrane pref-1 can be processed to generate an inhibitory soluble form, thereby greatly extending its range of action. Furthermore, we present evidence that alternate splicing is the mechanism that governs the production of transmembrane versus soluble pref-1, thereby determining the mode of action, juxtacrine or paracrine, of the pref-1 protein.


2020 ◽  
Vol 62 (6) ◽  
pp. 854-863
Author(s):  
Su-Young Choi ◽  
Su Yeon Lee ◽  
Da hye Jang ◽  
Suk Jun Lee ◽  
Jeong-Yong Cho ◽  
...  

2017 ◽  
Vol 95 ◽  
pp. 589-598 ◽  
Author(s):  
Chang Won Lee ◽  
Jeong Yeon Seo ◽  
Jisun Lee ◽  
Ji Won Choi ◽  
Sarang Cho ◽  
...  

2013 ◽  
Vol 2013 ◽  
pp. 1-12 ◽  
Author(s):  
Dong Hoon Kwak ◽  
Ji-Hye Lee ◽  
Dong-Gun Kim ◽  
Taesoo Kim ◽  
Kwang Jin Lee ◽  
...  

Hwangryunhaedok-tang (HRT) has been long used as traditional medicine in Asia. However, inhibitory role of HRT is unclear in early stage of 3T3-L1 adipocyte differentiation related to signaling. In the present study, we investigated the inhibitory effects of HRT on upstream signaling of peroxisome proliferation-activity receptor-γ(PPAR-γ) and CCAAT/enhancer binding protein-β(C/EBP-β) expression in differentiation of 3T3-L1 preadipocytes. We found that HRT significantly inhibited the adipocyte differentiation by downregulating several adipocyte-specific transcription factors including PPAR-γ, C/EBP-α, and C/EBP-βin 3T3-L1 preadipocytes. Furthermore, we observed that HRT markedly inhibited the differentiation media-mediated phosphorylation of Raf/extracellular mitogen-activated protein kinase 1 (MEK1)/signal-regulated protein kinase 1/2 (ERK1/2) and phosphorylation of phosphoinositide-dependent kinase 1 (PDK1)/Akt. These results indicate that anti-adipogenesis mechanism involves the downregulation of the major transcription factors of adipogenesis including PPAR-γand C/EBP-αthrough inhibition of Raf/MEK1/ERK1/2 phosphorylation and PDK1/Akt phosphorylation by HRT. Furthermore, high performance liquid chromatography (HPLC) analysis showed HRT contains active antiobesity constituents such as palmatine, berberine, geniposide, baicalin, baicalein, and wogonin. Taken together, this study suggested that anti-adipogenesis effects of HRT were accounted by downregulation of Raf/MEK1/ERK1/2 pathway and PDK1/Akt pathway during 3T3-L1 adipocyte differentiation.


2010 ◽  
Vol 33 (9) ◽  
pp. 1610-1614 ◽  
Author(s):  
Eunjin Shin ◽  
Kyeong-Mi Choi ◽  
Hwan-Soo Yoo ◽  
Chong-Kil Lee ◽  
Bang Yeon Hwang ◽  
...  

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