Laboratory of Immunobiology, School of Life Sciences and Biotechnology, College of Natural Sciences, Kyungpook National University, Daegu, Korea.
Phytother Res. 2011 May;25(5):724-31. doi: 10.1002/ptr.3329. Epub 2010 Nov 12.
The effect of mollugin, isolated from the roots of Rubia cordifolia L., on cell viability, apoptosis and adipogenesis in 3T3-L1 preadipocytes was investigated. The inhibitory effect of mollugin (40-60 µM) on cell viability was more significant in differentiated adipocytes than in 3T3-L1 preadipocytes. In 3T3-L1 cells, the cytotoxicity of mollugin was accompanied by apoptotic events including mitochondrial membrane potential (Δψm) loss and activation of caspase-9, -3 and -7, leading to PARP degradation. Although the presence of 20 µM mollugin during induced adipocytic differentiation of 3T3-L1 cells for 6 days failed to affect the cell viability, it could almost completely abrogate the differentiation-associated morphology change and intracellular lipid accumulation. A similar level of inhibition was observed, when 20 µM mollugin was present during the early stage (D0-D2) of the differentiation period. In addition, the expression of C/EBPα, PPARγ1 and PPARγ2 was significantly down-regulated. The presence of 20 µM mollugin during either middle stage (D2-D4) or late stage (D4-D6) of the differentiation period, however, caused the inhibition to a lesser extent. These results indicated that mollugin at high concentrations (40-60 µM) exerted cytotoxicity via inducing apoptosis, whereas mollugin at a low concentration (20 µM) suppressed adipocytic differentiation without exerting cytotoxicity in 3T3-L1 preadipocytes.
从茜草根中分离得到的醉椒素对 3T3-L1 前脂肪细胞活力、细胞凋亡和脂肪生成的影响。醉椒素(40-60μM)对分化的脂肪细胞活力的抑制作用比对 3T3-L1 前脂肪细胞的抑制作用更为显著。在 3T3-L1 细胞中,醉椒素的细胞毒性伴随着细胞凋亡事件,包括线粒体膜电位(Δψm)丧失和 caspase-9、-3 和 -7 的激活,导致 PARP 降解。尽管在 3T3-L1 细胞诱导脂肪细胞分化的 6 天中存在 20μM 醉椒素不会影响细胞活力,但它几乎可以完全阻止分化相关的形态变化和细胞内脂质积累。当在分化期的早期(D0-D2)存在 20μM 醉椒素时,观察到相似水平的抑制。此外,C/EBPα、PPARγ1 和 PPARγ2 的表达显著下调。然而,在分化期的中期(D2-D4)或晚期(D4-D6)存在 20μM 醉椒素时,抑制作用程度较小。这些结果表明,高浓度(40-60μM)的醉椒素通过诱导细胞凋亡发挥细胞毒性,而低浓度(20μM)的醉椒素在 3T3-L1 前脂肪细胞中不发挥细胞毒性,抑制脂肪细胞分化。