Woo Sangee, Yoon Miso, Kim Jeongjun, Hong Yeonhee, Kim Min-Young, Shin Soon Shik, Yoon Michung
Department of Biomedical Engineering, Mokwon University, Daejeon 302-729, Republic of Korea.
AngioLab, Inc., Daejeon 305-509, Republic of Korea.
J Ethnopharmacol. 2016 Feb 3;178:238-50. doi: 10.1016/j.jep.2015.12.015. Epub 2015 Dec 15.
Melissa officinalis L. (Labiatae; lemon balm) has been used traditionally and contemporarily as an anti-stress herb. Current hypotheses suggest that not only chronic stress promotes angiogenesis, but angiogenesis also modulates adipogenesis and obesity. Because the herbal extract ALS-L1023 from M. officinalis L. (Labiatae; lemon balm) has an anti-angiogenic activity, we hypothesized that ALS-L1023 could inhibit adipogenesis and adipocyte hypertrophy.
ALS-L1023 was prepared by a two-step organic solvent fractionation from M. officinalis. The effects of ALS-L1023 on adipogenesis in 3T3-L1 adipocytes and adipocyte hypertrophy in high fat diet (HFD)-fed obese mice were measured using in vivo and in vitro approaches.
ALS-L1023 inhibited angiogenesis in a dose-dependent manner in the HUVEC tube formation assay in vitro. Treatment of cells with ALS-L1023 inhibited lipid accumulation and adipocyte-specific gene expression caused by troglitazone or MDI differentiation mix. ALS-L1023 reduced mRNA expression of angiogenic factors (VEGF-A and FGF-2) and MMPs (MMP-2 and MMP-9) in differentiated cells. In contrast, mRNA levels of angiogenic inhibitors (TSP-1, TIMP-1, and TIMP-2) increased. Protease activity, as measured by zymography, showed that activity of MMP-2 and MMP-9 decreased in ALS-L1023-treated cells. ALS-L1023 also inhibited MMP-2 and MMP-9 reporter gene expression in the presence of the MMP inducer phorbol 12-myristate 13-acetate. An in vivo study showed that ALS-L1023 not only decreased adipose tissue mass and adipocyte size, but also reduced mRNA levels of adipose tissue angiogenic factors and MMPs in HFD-fed obese mice.
These results suggest that the anti-angiogenic herbal extract ALS-L1023 suppresses adipogenesis and adipocyte hypertrophy, and this effect may be mediated by inhibiting angiogenesis and MMP activities. Thus, by curbing adipogenesis, anti-angiogenic ALS-L1023 yields a possible therapeutic choice for the prevention and treatment of human obesity and its associated conditions.
香蜂草(唇形科;柠檬香脂)在传统和现代都被用作抗应激草药。目前的假说表明,不仅慢性应激会促进血管生成,而且血管生成也会调节脂肪生成和肥胖。由于来自香蜂草的草药提取物ALS-L1023具有抗血管生成活性,我们推测ALS-L1023可能抑制脂肪生成和脂肪细胞肥大。
通过两步有机溶剂分级分离法从香蜂草中制备ALS-L1023。使用体内和体外方法测量ALS-L1023对3T3-L1脂肪细胞脂肪生成和高脂饮食(HFD)喂养的肥胖小鼠脂肪细胞肥大的影响。
在体外人脐静脉内皮细胞管形成试验中,ALS-L1023以剂量依赖性方式抑制血管生成。用ALS-L1023处理细胞可抑制由曲格列酮或MDI分化混合物引起的脂质积累和脂肪细胞特异性基因表达。ALS-L1023降低了分化细胞中血管生成因子(VEGF-A和FGF-2)和基质金属蛋白酶(MMP-2和MMP-9)的mRNA表达。相反,血管生成抑制剂(TSP-1、TIMP-1和TIMP-2)的mRNA水平升高。通过酶谱法测量的蛋白酶活性表明,在ALS-L1023处理的细胞中,MMP-2和MMP-9的活性降低。在存在MMP诱导剂佛波醇12-肉豆蔻酸酯13-乙酸酯的情况下,ALS-L1023也抑制MMP-2和MMP-9报告基因表达。一项体内研究表明,ALS-L1023不仅降低了HFD喂养的肥胖小鼠的脂肪组织质量和脂肪细胞大小,还降低了脂肪组织血管生成因子和MMPs的mRNA水平。
这些结果表明,抗血管生成草药提取物ALS-L1023抑制脂肪生成和脂肪细胞肥大,这种作用可能是通过抑制血管生成和MMP活性介导的。因此,通过抑制脂肪生成,抗血管生成的ALS-L1023为预防和治疗人类肥胖及其相关病症提供了一种可能的治疗选择。