Department of Pharmacology, Louisiana State University Health Science Center, New Orleans, Louisiana, West Virginia 25755, USA.
J Med Food. 2009 Oct;12(5):1074-83. doi: 10.1089/jmf.2008.0230.
Adiponectin is an adipokine secreted by differentiated adipocytes. Clinical studies suggest a negative correlation between oxidative stress and adiponectin levels in patients with metabolic syndrome or cardiovascular disease. Natural compounds that can prevent oxidative stress mediated inhibition of adiponectin may be potentially therapeutic. Boldine, an aporphine alkaloid abundant in the medicinal plant Peumus boldus, is a powerful antioxidant. The current study demonstrates the effects of boldine on the expression of adiponectin and its regulators, CCAAT/enhancer binding protein-alpha (C/EBPalpha) and peroxisome proliferator-activated receptor (PPAR)-gamma, in 3T3-L1 cells. Differentiated 3T3-L1 adipocytes were exposed to either hydrogen peroxide (H(2)O(2)) (100 microM) or tumor necrosis factor-alpha (TNFalpha) (1 ng/mL) for 24 hours in the presence or absence of increasing concentrations of boldine (5-100 microM). Quantitative polymerase chain reaction showed that both the oxidants decreased the mRNA levels of adiponectin, PPARgamma, and C/EBPalpha to half of the control levels. Boldine, at all concentrations, counteracted the inhibitory effect of H(2)O(2) or TNFalpha and increased the expression of adiponectin and its regulators. The effect of boldine on adiponectin expression was biphasic, with the lower concentrations (5-25 microM) having a larger inductive effect compared to higher concentrations (50-100 microM). Boldine treatment alone in the absence of H(2)O(2) or TNFalpha was also able to induce adiponectin at the inductive phase of adipogenesis. Peroxisome proliferator response element-luciferase promoter transactivity analysis showed that boldine interacts with the PPAR response element and could potentially modulate PPAR responsive genes. Our results indicate that boldine is able to modulate the expression of adiponectin and its regulators in 3T3-L1 cells and has the potential to be beneficial in obesity-related cardiovascular disease.
脂联素是一种由分化的脂肪细胞分泌的脂肪因子。临床研究表明,在代谢综合征或心血管疾病患者中,氧化应激与脂联素水平呈负相关。能够预防氧化应激介导的脂联素抑制的天然化合物可能具有潜在的治疗作用。波多因,一种丰富于药用植物 Peumus boldus 中的阿朴啡生物碱,是一种强大的抗氧化剂。本研究表明,波多因对 3T3-L1 细胞中脂联素及其调节因子 CCAAT/增强子结合蛋白-α(C/EBPα)和过氧化物酶体增殖物激活受体(PPAR)-γ的表达的影响。分化的 3T3-L1 脂肪细胞在存在或不存在增加浓度的波多因(5-100 μM)的情况下,分别用过氧化氢(H2O2)(100 μM)或肿瘤坏死因子-α(TNFα)(1ng/ml)处理 24 小时。定量聚合酶链反应显示,两种氧化剂均使脂联素、PPARγ和 C/EBPα 的 mRNA 水平降低至对照水平的一半。波多因在所有浓度下均能拮抗 H2O2 或 TNFα 的抑制作用,并增加脂联素及其调节因子的表达。波多因对脂联素表达的影响呈双相性,较低浓度(5-25 μM)比较高浓度(50-100 μM)具有更大的诱导作用。在没有 H2O2 或 TNFα 的情况下,波多因单独处理也能在脂肪生成的诱导阶段诱导脂联素。过氧化物酶体增殖物反应元件-荧光素酶启动子转录活性分析表明,波多因与 PPAR 反应元件相互作用,可能调节 PPAR 反应基因。我们的结果表明,波多因能够调节 3T3-L1 细胞中脂联素及其调节因子的表达,并有潜力在肥胖相关的心血管疾病中发挥作用。