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齐墩果酸可降低 3T3-L1 脂肪细胞的分化标志物。

Oleanolic acid reduces markers of differentiation in 3T3-L1 adipocytes.

机构信息

Department of Food Science and Nutrition and Regional Research Universities Program/Medical and Bio-Materials Research Center, Hallym University, Chuncheon, Kangwon-do 200-702, South Korea.

出版信息

Nutr Res. 2010 Dec;30(12):831-9. doi: 10.1016/j.nutres.2010.10.001.

Abstract

Oleanolic acid is a triterpenoid compound that is widely present in vegetables, medicinal herbs, and other plants and has potent antioxidant and antiinflammatory properties. However, the potential of oleanolic acid to offset obesity is not clear. This study tested the hypothesis that oleanolic acid suppresses the differentiation of 3T3-L1 adipocytes by downregulating cellular induction of peroxisome proliferators-activated receptor γ (PPARγ) and cytidine-cytidine-adenosine-adenosine-thymidine (CCAAT) enhancer binding protein α (C/EBPα). The 3T3-L1 adipocytes were cultured and differentiated in Dulbecco modified Eagle medium containing 10% fetal bovine serum for 6 to 8 days in the absence and presence of 1 to 25 μmol/L oleanolic acid according to differentiating protocols. Nontoxic oleanolic acid, at 25 μmol/L or less, dose-dependently attenuated lipid accumulation in differentiated adipocytes as evidenced by Oil Red O staining. Western blot analysis showed that the induction of PPARγ and C/EBPα was markedly attenuated in differentiated and oleanolic acid-treated adipocytes at their transcriptional messenger RNA levels. Furthermore, this study examined whether oleanolic acid dampened the induction of visfatin, a proinflammatory and visceral fat-specific adipokine expressed in adipocytes. Visfatin expression was inhibited in differentiated adipocytes exposed to a PPARγ inhibitor GW9662. In addition, the visfatin production was significantly repressed in 25 μmol/L oleanolic acid-treated adipocytes, possibly through blocking PPARγ activation. These results demonstrate that oleanolic acid may be a promising agent to disturb adipocyte differentiation and suppress obesity-associated inflammation.

摘要

齐墩果酸是一种广泛存在于蔬菜、草药和其他植物中的三萜化合物,具有强大的抗氧化和抗炎特性。然而,齐墩果酸抵消肥胖的潜力尚不清楚。本研究检验了以下假设:齐墩果酸通过下调过氧化物酶体增殖物激活受体 γ(PPARγ)和胞嘧啶-胞嘧啶-腺苷-腺苷-胸腺嘧啶(CCAAT)增强子结合蛋白 α(C/EBPα)的细胞诱导来抑制 3T3-L1 脂肪细胞的分化。根据分化方案,将 3T3-L1 脂肪细胞在含有 10%胎牛血清的 Dulbecco 改良 Eagle 培养基中培养和分化 6 至 8 天,有无 1 至 25 μmol/L 齐墩果酸。非毒性齐墩果酸,在 25 μmol/L 或更低剂量下,剂量依赖性地减弱了分化脂肪细胞中的脂质积累,如油红 O 染色所示。Western blot 分析表明,在分化和齐墩果酸处理的脂肪细胞中,PPARγ 和 C/EBPα 的诱导在转录信使 RNA 水平上明显减弱。此外,本研究还检查了齐墩果酸是否减弱了内脏脂肪特异性脂肪细胞因子 visfatin 的诱导。在分化的脂肪细胞中,PPARγ 抑制剂 GW9662 显著抑制了 visfatin 的表达。此外,在 25 μmol/L 齐墩果酸处理的脂肪细胞中,visfatin 的产生明显受到抑制,可能是通过阻断 PPARγ 激活。这些结果表明,齐墩果酸可能是一种有前途的干扰脂肪细胞分化和抑制肥胖相关炎症的药物。

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