Methanol extract of Elsholtzia fruticosa promotes 3T3-L1 preadipocyte differentiation.
Deumaya ShresthaEunbin KimKrishna K ShresthaSung-Suk SuhSung Hak KimJong Bae SeoPublished in: Journal of animal science and technology (2024)
Elsholtzia fruticosa (EF) is present in tropical regions throughout South Asian countries as well as the Himalayas. Although it has been used as a traditional medicine to treat digestive, respiratory, and inflammatory issues, its effect on preadipocyte differentiation is unknown. In this study, we examined the effects of a methanol extract prepared from EF on the differentiation of 3T3-L1 preadipocytes. Cell differentiation was assessed by microscopic observation and oil-red O staining. The expression of adipogenic and lipogenic genes, including PPARγ and C/EBPα , was measured by western blot analysis and quantitative real-time polymerase chain reaction (qRT-PCR), to provide insight into adipogenesis and lipogenesis mechanisms. The results indicated that EF promotes the differentiation of 3T3-L1 preadipocytes, with elevated lipid accumulation occurring in a concentration-dependent manner without apparent cytotoxicity. EF enhances the expression of adipogenic and lipogenic genes, including PPARγ , FABP4 , adiponectin , and FAS , at the mRNA and protein levels. The effect of EF was more pronounced during the early and middle stages of 3T3-L1 cell differentiation. Treatment with EF decreased C/EBP homologous protein (CHOP) mRNA and protein levels, while increasing C/EBPα and PPARγ expression. Treatment with EF resulted in the upregulation of cyclin E and CDK2 gene expression within 24 h, followed by a decrease at 48 h, demonstrating the early-stage impact of EF. A concomitant increase in cyclin-D1 levels was observed compared with untreated cells, indicating that EF modulates lipogenic and adipogenic genes through intricate mechanisms involving CHOP and cell cycle pathways. In summary, EF induces the differentiation of 3T3-L1 preadipocytes by increasing the expression of adipogenic and lipogenic genes, possibly through CHOP and cell cycle-dependent mechanisms.
Keyphrases
- cell cycle
- poor prognosis
- binding protein
- cell proliferation
- gene expression
- early stage
- genome wide
- oxidative stress
- insulin resistance
- diffuse large b cell lymphoma
- long non coding rna
- metabolic syndrome
- dna methylation
- fatty acid
- induced apoptosis
- dna damage
- signaling pathway
- south africa
- magnetic resonance
- climate change
- amino acid
- combination therapy
- cell cycle arrest
- dna repair
- computed tomography
- small molecule
- carbon dioxide