Abstract
Purposes: Nuciferine, a main aporphine alkaloid component found in lotus leaf (Nelumbo nucifera), has been demonstrated to possess the property of reducing fat mass and alleviating dyslipidemia in vivo. The purpose of this study is to explore the effects of nuciferine on the proliferation and differentiation of 3T3-L1 cells and further investigate the possible underlying molecular mechanisms. Methods: 3T3-L1 preadipocytes were treated with 0∼20 μM nuciferine for 24∼120 h, the cell viability was assessed using CCK8. 3T3-L1 preadipocytes and human primary preadipocytes were then induced differentiation and the effects of nuciferine on the lipid metabolism in differentiating and fully differentiated adipocytes were observed by the methods of intracellular triglyceride (TG) assay, Oil Red O staining, RT-qPCR and western blot. Transient transfection and dual luciferase reporter gene methods were used to assess the effects of nuciferine on FAS promoter activities. Results: Nuciferine inhibited the proliferation of 3T3-L1 preadipocytes in a dose- and time-dependent manner. 20 μM nuciferine significantly attenuated lipid accumulation and reduced intracellular TG contents by 47.2, 59.9 and 55.4% on the third, sixth and ninth day of preadipocytes differentiation, respectively (all p < 0.05). Moreover, the mRNA levels of PPARγ, C/EBPα, C/EBPβ, FAS, ACC, HSL and ATGL were notably decreased by 39.2∼92.5% in differentiating preadipocytes when treated with 5∼20 μM nuciferine (all p < 0.05). In fully differentiated adipocytes treated with 20 μM nuciferine for 48 h, the mRNA levels of FAS, ACC and SREBP1 were remarkably downregulated by 22.6∼45.2% compared with the controls (0 μM) (all p < 0.05), whereas the expression of adipokines FGF21 and ZAG were notably promoted by nuciferine. Similarly, in fully differentiated human primary adipocytes, the mRNA levels of FAS, ACC, SREBP1 were decreased and the expression of FGF21 and ZAG were elevated after treated with nuciferine (all p < 0.05). Further mechanism studies showed that 2.5∼20 μM nuciferine significantly decreased FAS promoter activities in 3T3-L1 preadipocytes. Conclusion: Nuciferine inhibited the proliferation and differentiation of 3T3-L1 preadipocytes. The inhibitory effects of nuciferine on adipogenesis might be due to the downregulation of PPARγ, C/EBPα and C/EBPβ, which led to the reduction of intracellular lipid accumulation in 3T3-L1 cells and by downregulating the expression of critical lipogenic enzymes, especially of FAS, which was achieved by inhibiting the FAS promoter activities. Besides, nuciferine promoted the expression of adipokines in fully differentiated adipocytes.
Highlights
Obesity is a wide spread chronic disease which is becoming one of the major risk factors for various diseases including cardiovascular diseases, type 2 diabetes and tumors
3T3-L1 preadipocytes were treated with 0∼20 μM nuciferine for 24∼120 h
The maximal inhibition effect was observed at 20 μM nuciferine for 120h, where the cell viability rate was 39.7% lower than that of the control cells (0 μM) (Figure 2B, p < 0.05). These results indicate that the proliferation of 3T3-L1 preadipocytes was gradually and sustainably inhibited by nuciferine treatment in a dose- and timedependent manner
Summary
Obesity is a wide spread chronic disease which is becoming one of the major risk factors for various diseases including cardiovascular diseases, type 2 diabetes and tumors. It is characterized by excessive triglyceride (TG) accumulation resulting from increased food intake and/or lessened energy consumption. The number and the size of mature adipocytes reflects the overall volume of fat mass (White and Ravussin, 2019). Fat depots expands by increasing the number of adipocytes and the size of average fat cell volume, regulating proliferation and differentiation of preadipocytes establishes a new therapeutic target for obesity and related complications (White and Ravussin, 2019). 3T3-L1 preadipocyte line was selected as it is known to be one of the most characterized cell lines used in studying the molecular mechanism involved in the proliferation and differentiation of adipocytes (Liu et al, 2017)
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