Department of Food Science and Nutrition, Hallym University, Chuncheon, Kangwon-do 200-702, Republic of Korea.
Chem Biol Interact. 2010 Dec 5;188(3):457-66. doi: 10.1016/j.cbi.2010.09.017. Epub 2010 Sep 21.
Many benzo[b]furan lignans are known to be biologically active in nature. 2-(3'-Methoxy-4'-hydroxy-phenyl)-5-(3-hydroxypropyl)-7-methoxy-benzo[b]furan-3-carbaldehyde (XH-14) is found as a bioactive component isolated from the plant Salvia miltiorrhiza, commonly known as Danshen, which is a traditional Chinese medicine that is used as a cardiovascular medication. This study examined whether 3 different XH-14 derivatives can inhibit adipocyte differentiation and induction of the adipokines visfatin and resistin in 3T3-L1 adipocytes. Adipocytes were cultured and differentiated in Dulbecco's modified Eagle medium containing fetal bovine serum, 3-isobytyl-1-methylxanthine, dexamethasone, and insulin for 6-8d in the absence and presence of 1-25μM XH-14-derived benzo[b]furan derivatives. Nontoxic 2-(3'-methoxy-4'-hydroxy-phenyl)-6-(3-hydroxypropyl)-5-methoxy-benzo[b]furan (5-MBF) at ≥5μM attenuated cellular lipid accumulation and down-regulated induction of peroxisome proliferator activated receptors γ (PPARγ) and CCAAT enhancer binding protein α (C/EBPα) in a dose-dependent manner, as evidenced by Oil Red O staining and Western blot analysis. Such inhibition of PPAR( and C/EBP( by 5-MBF was achieved at transcriptional mRNA levels. However, 2-(3'-methoxy-4'-hydroxy-phenyl)-5-(3-hydroxypropyl)-7-methoxy-benzo[b]furan (7-MBF) and 2-(3'-methoxy-4'-hydroxy-phenyl)-5-(3-hydroxypropyl)-7-methoxy-benzo[b]furan (6-MBF) had minimal effects on adipogenic differentiation, suggesting a structure-activity relationship of methoxybenzo[b]furan derivatives as an inhibitor of adipogenic differentiation. Furthermore, ≥5μM 5-MBF retarded protein and mRNA expression of proinflammatory and insulin resistance-enhancing adipokines of visfatin and resistin in differentiated adipocytes. Induction of visfatin and resistin was, at least in part, mediated via adipocyte differentiation-associated activation of PPARγ signal targeting adipocyte protein 2 and stearoyl-CoA desaturase. These results demonstrate that the 2-(3'-methoxy-4'-hydroxy-phenyl)-3-hydroxypropyl benzo[b]furan lignan, with a methoxy group at the 5-position on the benzene ring, may be a promising agent for disturbance of adipogenic differentiation and for blockage of obesity-associated inflammatory and metabolic diseases.
许多苯并[b]呋喃木脂素在自然界中具有生物活性。2-(3'-甲氧基-4'-羟基-苯基)-5-(3-羟丙基)-7-甲氧基苯并[b]呋喃-3-甲醛(XH-14)是从丹参植物中分离出的生物活性成分,丹参是一种传统的中药,用作心血管药物。本研究探讨了 3 种不同的 XH-14 衍生物是否可以抑制 3T3-L1 脂肪细胞中的脂肪细胞分化和脂联素和抵抗素的诱导。脂肪细胞在含有胎牛血清、3-异丁基-1-甲基黄嘌呤、地塞米松和胰岛素的 Dulbecco 改良 Eagle 培养基中培养并分化 6-8d,在不存在和存在 1-25μM XH-14 衍生的苯并[b]呋喃衍生物的情况下。非毒性 2-(3'-甲氧基-4'-羟基-苯基)-6-(3-羟丙基)-5-甲氧基苯并[b]呋喃(5-MBF)在≥5μM 时以剂量依赖性方式减弱细胞脂质积累,并下调过氧化物酶体增殖物激活受体γ(PPARγ)和 CCAAT 增强子结合蛋白α(C/EBPα)的诱导,如油红 O 染色和 Western blot 分析所示。5-MBF 对 PPAR(和 C/EBP(的这种抑制作用在转录 mRNA 水平上实现。然而,2-(3'-甲氧基-4'-羟基-苯基)-5-(3-羟丙基)-7-甲氧基苯并[b]呋喃(7-MBF)和 2-(3'-甲氧基-4'-羟基-苯基)-5-(3-羟丙基)-7-甲氧基苯并[b]呋喃(6-MBF)对脂肪生成分化的影响最小,这表明甲氧基苯并[b]呋喃衍生物作为脂肪生成分化抑制剂的结构-活性关系。此外,≥5μM 5-MBF 延迟了分化脂肪细胞中促炎和胰岛素抵抗增强的脂肪细胞因子脂联素和抵抗素的蛋白和 mRNA 表达。脂联素和抵抗素的诱导至少部分是通过脂肪细胞分化相关的靶向脂肪细胞蛋白 2 和硬脂酰辅酶 A 去饱和酶的 PPARγ信号介导的。这些结果表明,具有苯环 5 位甲氧基的 2-(3'-甲氧基-4'-羟基-苯基)-3-羟丙基苯并[b]呋喃木脂素可能是一种有前途的药物,可用于干扰脂肪生成分化,并阻断肥胖相关的炎症和代谢性疾病。