Department of Pharmacognosy and Phytochemistry, Meiji Pharmaceutical University, 2-522-1 Noshio, Kiyose, Tokyo 204-8588, Japan.
Research Institute of Pharmaceutical Science, Musashino University, 1-1-20 Shinmachi Nishitokyo-shi, Tokyo 202-8585, Japan.
Phytomedicine. 2014 May 15;21(6):800-6. doi: 10.1016/j.phymed.2014.01.014. Epub 2014 Mar 11.
We previously demonstrated that ethyl acetate extracts of Kaempferia parviflora Wall. Ex Baker (KPE) improve insulin resistance in TSOD mice and showed that its components induce differentiation and adipogenesis in 3T3-L1 preadipocytes. The present study was undertaken to examine whether KPE and its isolated twelve components suppress further lipid accumulation in 3T3-L1 mature adipocytes. KPE reduced intracellular triglycerides in mature adipocytes, as did two of its components, 3,5,7,3',4'-pentamethoxyflavone and 5,7,4'-trimethoxyflavone. Shrinkage of lipid droplets in mature adipocytes was observed, and mRNA expression levels of adipose tissue triglyceride lipase (ATGL) and hormone-sensitive lipase (HSL) were up-regulated by these two polymethoxyflavonoids (PMFs). Furthermore, the protein expression level of ATGL and the release level of glycerol into the cell culture medium increased. In contrast, the peroxisome proliferator-activated receptor γ (PPARγ) agonist, troglitazone, did not decrease intracellular triglycerides in mature adipocytes, and the mRNA expression level of PPARγ was not up-regulated in mature adipocytes treated with the two active PMFs. Therefore, suppression of lipid accumulation in mature adipocytes is unlikely to be enhanced by transcriptional activation of PPARγ. These results suggest that KPE and its active components enhance lipolysis in mature adipocytes by activation of ATGL and HSL independent of PPARγ transcription, thus preventing adipocyte hypertrophy. On the other hand, the full hydroxylated flavonoid quercetin did not show the suppressive effects of lipid accumulation in mature adipocyte in the same conditions. Consequently, methoxy groups in the flavones are important for the activity.
我们之前已经证明,山柰酚二甲醚提取物(KPE)可以改善 TSOD 小鼠的胰岛素抵抗,并表明其成分可以诱导 3T3-L1 前脂肪细胞分化和脂肪生成。本研究旨在研究 KPE 及其 12 种分离成分是否能抑制 3T3-L1 成熟脂肪细胞中进一步的脂质积累。KPE 和两种成分(3,5,7,3',4'-五甲氧基黄酮和 5,7,4'-三甲氧基黄酮)可减少成熟脂肪细胞中的细胞内甘油三酯。成熟脂肪细胞中脂质滴收缩,两种多甲氧基黄酮(PMFs)上调脂肪组织甘油三酯脂肪酶(ATGL)和激素敏感脂肪酶(HSL)的 mRNA 表达水平。此外,ATGL 的蛋白表达水平和甘油向细胞培养液中的释放水平增加。相比之下,过氧化物酶体增殖物激活受体γ(PPARγ)激动剂曲格列酮并不能减少成熟脂肪细胞中的细胞内甘油三酯,用两种活性 PMFs 处理的成熟脂肪细胞中 PPARγ 的 mRNA 表达水平也没有上调。因此,PPARγ 的转录激活不太可能增强成熟脂肪细胞中脂质积累的抑制作用。这些结果表明,KPE 及其活性成分通过激活 ATGL 和 HSL 增强成熟脂肪细胞中的脂肪分解,而不依赖于 PPARγ 转录,从而防止脂肪细胞肥大。另一方面,全羟基化黄酮槲皮素在相同条件下并未显示出抑制成熟脂肪细胞中脂质积累的作用。因此,类黄酮中的甲氧基对于活性很重要。