Department of Nutritional Biochemistry, School of Nutrition and Dietetics, Kanagawa University of Human Services, 1-10-1 Heisei-cho, Yokosuka, Kanagawa 238-8522, Japan.
Med Chem. 2011 Jul;7(4):250-6. doi: 10.2174/157340611796150950.
Adiponectin, an adipose-derived protein, shows insulin-sensitizing, anti-diabetic and anti-atherogenic activities, which implies that the protein represents a potential target to improve lifestyle-related diseases like type 2 diabetes. Based on our hypothesis that agents that cause adipocyte differentiation could also act as adiponectin secretion enhancers, we screened butanol extracts of 96 fungus culture extracts for their differentiation-inducing activity in ST-13 preadipocytes. We found that the butanol extract of a fungus P16 culture extract possessed such an activity, and isolated norlichexanthone as an active compound through activity-guided fractionation. Oil red O staining showed that norlichexanthone induced adipogenesis in ST-13 cells. Its differentiation-inducing activity was supported by the observation that norlichexanthone dose-dependently increased the mRNA expression of fatty acid-binding protein and peroxisome proliferator activated receptor γ (PPARγ), markers of adipocyte differentiation. Western blot analysis demonstrated that the compound enhanced the secretion of adiponectin protein in a dose-dependent manner. An increase in mRNA expression of adiponectin was also observed in the norlichexanthone-treated ST-13 cells. Actinomycin D treatment blocked the enhancement of adiponectin mRNA expression by norlichexanthone, suggesting that it is the result of increased transcription. A luciferase reporter assay indicated that norlichexanthone was unlikely to be an agonist of PPARγ, implying that its action of mechanism might differ from those of thiazolidinediones which upregulate adiponectin expression via activation of PPARγ. These findings suggest the possibility that norlichexanthone has the potential to treat and/or prevent lifestyle-related diseases, including metabolic syndrome, type 2 diabetes, atherosclerosis and cardiovascular diseases.
脂联素是一种脂肪衍生的蛋白质,具有胰岛素增敏、抗糖尿病和抗动脉粥样硬化作用,这意味着该蛋白代表了改善与生活方式相关疾病(如 2 型糖尿病)的潜在靶点。基于我们的假设,即导致脂肪细胞分化的物质也可以作为脂联素分泌增强剂,我们筛选了 96 种真菌培养物的丁醇提取物,以寻找其对 ST-13 前体脂肪细胞的分化诱导活性。我们发现,真菌 P16 培养物的丁醇提取物具有这种活性,并通过活性导向分离分离出了诺里二氢黄酮作为活性化合物。油红 O 染色显示,诺里二氢黄酮可诱导 ST-13 细胞脂肪生成。其分化诱导活性得到了以下观察结果的支持:诺里二氢黄酮可剂量依赖性增加脂肪酸结合蛋白和过氧化物酶体增殖物激活受体 γ(PPARγ)mRNA 的表达,这是脂肪细胞分化的标志物。Western blot 分析表明,该化合物以剂量依赖性方式增强脂联素蛋白的分泌。在诺里二氢黄酮处理的 ST-13 细胞中也观察到脂联素 mRNA 表达增加。放线菌酮处理阻断了诺里二氢黄酮对脂联素 mRNA 表达的增强作用,表明这是转录增加的结果。荧光素酶报告基因分析表明,诺里二氢黄酮不太可能是 PPARγ 的激动剂,这意味着其作用机制可能与噻唑烷二酮类不同,后者通过激活 PPARγ 上调脂联素表达。这些发现表明,诺里二氢黄酮有可能治疗和/或预防与生活方式相关的疾病,包括代谢综合征、2 型糖尿病、动脉粥样硬化和心血管疾病。