槐定碱通过 Src 介导的血管内皮生长因子受体表达和 PI3K/AKT 磷酸化抑制作用抵消肥胖症

Jingchun Sun, Xiaoting Wang, Yulin He, Xuekai Tian, Tiantian Yuan, Gongshe Yang, Taiyong Yu
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引用次数: 0

摘要

槐定碱(SRP)是一种天然喹嗪生物碱,存在于许多传统中草药中,但其对脂肪组织的影响尚不清楚。我们通过给高脂饮食(HFD)喂养的 C57BL/6 小鼠灌胃服用 SRP 来改善血清脂质水平。11 周后,补充 SRP 可显著降低体重增加,改善葡萄糖稳态,同时减少皮下脂肪和肝脏重量。SRP 还能抑制 3T3-L1 细胞的增殖和分化。蛋白质组学分析表明,SRP 通过与 Src 相互作用抑制脂肪细胞分化,从而抑制血管内皮生长因子受体 2(VEGFR2)的表达和 PI3K/AKT 磷酸化。这项研究为利用小分子治疗肥胖症提供了经验依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sophoridine Counteracts Obesity via Src-Mediated Inhibition of VEGFR Expression and PI3K/AKT Phosphorylation
Sophoridine (SRP) is a natural quinolizidine alkaloid found in many traditional Chinese herbs, though its effect on adipose tissue is unclear. We improved serum lipid levels by administering SRP by gavage in high-fat diet (HFD)-fed C57BL/6 mice. After 11 weeks, SRP supplementation significantly reduced body weight gain and improved glucose homeostasis, while reducing subcutaneous fat and liver weight. SRP also inhibited cell proliferation and differentiation of 3T3-L1 cells. Proteomics analysis revealed that SRP inhibits adipocyte differentiation by interacting with Src, thereby suppressing vascular endothelial growth factor receptor 2 (VEGFR2) expression and PI3K/AKT phosphorylation. This study provides an empirical basis for the treatment of obesity with small molecules.
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