Verapamil inhibits 3T3-L1 preadipocyte differentiation

Nan Gu , Shi Liu , Xirong Guo , Li Fei , Xiaoqin Pan , Mei Guo , Ronghua Chen
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Abstract

Objective

To investigate the effect of the calcium channel blocker verapamil on adipocyte differentiation and its mechanism of action.

Methods

Preadipocytes from 3T3-L1 strain mouse embryos were cultured and differentiated into matured adipocytes in vitro. Verapamil was added to the culture medium in the concentration of 30 μmol/L on Day 0. Cell differentiation was determined by Oil Red O staining and marker gene mRNA expression was evaluated and compared by RT-PCR. The fluo-3/AM probe and laser scanning confocal microscopy were used to measure intracellular calcium concentrations.

Results

The differentiation rate of 3T3-L1 preadipocytes exposed to verapamil was lower than that of untreated cells.
Verapamil promoted the retention of pref-1 gene expression. Lipoprotein lipase expression in the verapamil group was significantly lower than that in the control group on Day 4, Day 6 and Day 8 (P < 0.05) and resistin expression was significantly lower than that in the control group on Day 6, Day 8 and Day 10 (P < 0.05). Fatty acid synthase expression in the verapamil group was significantly lower than that in the control group from Day 2 (P < 0.05).
Intracellular concentrations of calcium [Ca2+]i in the verapamil group were significantly decreased compared with those in the control group on Day 2, Day 4 and Day 6 (P < 0.05), while there was no obvious difference between the two groups on Day 0 (P > 0.05).

Conclusion

In 3T3-L1 preadipocytes verapamil significantly reduced adipocyte differentiation, down-regulated the mRNA expression of three marker genes for adipocytes differentiation, and prolonged the mRNA expression of an inhibitor of differentiation. The inhibitory effect of verapamil on differentiation may involve its role as a blocker of calcium influx in adipocytes.

维拉帕米抑制3T3-L1前脂肪细胞分化
目的探讨钙通道阻滞剂维拉帕米对脂肪细胞分化的影响及其作用机制。方法体外培养3T3-L1系小鼠胚胎脂肪细胞,并将其分化为成熟脂肪细胞。第0天在培养基中加入维拉帕米,浓度为30 μmol/L。油红O染色检测细胞分化情况,RT-PCR检测标记基因mRNA表达水平。使用fluo-3/AM探针和激光扫描共聚焦显微镜测量细胞内钙浓度。结果维拉帕米处理的3T3-L1前脂肪细胞分化率低于未处理的细胞。维拉帕米促进pref-1基因表达的保留。维拉帕米组在第4天、第6天、第8天的脂蛋白脂肪酶表达量显著低于对照组(P <在第6天、第8天和第10天,抵抗素的表达显著低于对照组(P <0.05)。维拉帕米组脂肪酸合成酶的表达从第2天起显著低于对照组(P <0.05)。维拉帕米组细胞内钙[Ca2+]i浓度在第2天、第4天和第6天与对照组相比显著降低(P <0.05),而第0天两组间差异无统计学意义(P >0.05)。结论维拉帕米可显著抑制3T3-L1前脂肪细胞的分化,下调3个脂肪细胞分化标志基因的mRNA表达,延长1个分化抑制基因的mRNA表达。维拉帕米对分化的抑制作用可能涉及其作为脂肪细胞钙内流的阻滞剂的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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