首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Suppression of Lipid Accumulation by Indole-3-Carbinol Is Associated with Increased Expression of the Aryl Hydrocarbon Receptor and CYP1B1 Proteins in Adipocytes and with Decreased Adipocyte-Stimulated Endothelial Tube Formation
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Suppression of Lipid Accumulation by Indole-3-Carbinol Is Associated with Increased Expression of the Aryl Hydrocarbon Receptor and CYP1B1 Proteins in Adipocytes and with Decreased Adipocyte-Stimulated Endothelial Tube Formation

机译:吲哚-3-甲醇抑制脂质蓄积与脂肪细胞中芳烃受体和CYP1B1蛋白的表达增加以及脂肪细胞刺激的内皮管形成减少有关。

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摘要

This study investigated the effects of indole-3-carbinol (I3C) on adipogenesis- and angiogenesis-associated factors in mature adipocytes. The cross-talk between mature adipocytes and endothelial cells (ECs) was also explored by cultivating ECs in a conditioned medium (CM) by using I3C-treated adipocytes. The results revealed that I3C significantly inhibited triglyceride accumulation in mature adipocytes in association with significantly increased expression of AhR and CYP1B1 proteins as well as slightly decreased nuclear factor erythroid-derived factor 2–related factor 2, hormone-sensitive lipase, and glycerol-3-phosphate dehydrogenase expression by mature adipocytes. Furthermore, I3C inhibited CM-stimulated endothelial tube formation, which was accompanied by the modulated secretion of angiogenic factors in adipocytes, including vascular endothelial growth factor, interleukin-6, matrix metalloproteinases, and nitric oxide. In conclusion, I3C reduced lipid droplet accumulation in adipocytes and suppressed adipocyte-stimulated angiogenesis in ECs, suggesting that I3C is a potential therapeutic agent for treating obesity and obesity-associated disorders.
机译:这项研究调查了吲哚-3-甲醇(I3C)对成熟脂肪细胞中脂肪生成和血管生成相关因子的影响。还通过使用I3C处理的脂肪细胞在条件培养基(CM)中培养EC来探索成熟脂肪细胞与内皮细胞(EC)之间的串扰。结果显示,I3C显着抑制成熟脂肪细胞中甘油三酸酯的积聚,同时与AhR和CYP1B1蛋白的表达显着增加以及核因子类红血球衍生因子2相关因子2,激素敏感性脂肪酶和甘油3略有降低成熟脂肪细胞表达磷酸脱氢酶。此外,I3C抑制了CM刺激的内皮管形成,并伴随着脂肪细胞中血管生成因子的分泌调节,包括血管内皮生长因子,白介素6,基质金属蛋白酶和一氧化氮。总之,I3C减少了EC中脂肪细胞中脂质滴的积累,并抑制了EC中脂肪细胞刺激的血管生成,这表明I3C是治疗肥胖和肥胖相关疾病的潜在治疗剂。

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