天然产物圆霉菌酸通过抑制PTP1B治疗衰老和肥胖

Life medicine Pub Date : 2022-10-26 eCollection Date: 2022-12-01 DOI:10.1093/lifemedi/lnac044
Jie Zhu, Yongpan An, Xin Wang, Liting Huang, Weikaixin Kong, Miaomiao Gao, Jingxiang Wang, Xinpei Sun, Sujie Zhu, Zhengwei Xie
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引用次数: 0

摘要

肥胖的发生与年龄有关。但它们之间的相互作用仍然是个谜。在这里,我们发现圆形酸(RA),一种植物衍生的五环三萜,是一种强大的抗衰老和治疗肥胖的药物。考虑到肥胖个体降低了瘦素导致肥胖的食欲抑制和能量消耗增强功能,我们发现RA是一种瘦素增敏剂,通过观察RA增强了瘦素对正常饮食诱导肥胖(DIO)小鼠的敏感性,而对正常瘦小鼠、瘦素受体缺陷(db/db)小鼠和瘦素缺陷(ob/ob)小鼠的作用很小或没有作用。同时,RA通过增强瘦素敏感性,显著增加了DIO小鼠的能量消耗、BAT产热和葡萄糖代谢。关于作用方式,我们证明了RA是瘦素负调节蛋白酪氨酸磷酸酶1B (PTP1B)和t细胞PTP (TCPTP)的非竞争性抑制剂,通过与它们的c端相互作用,从而通过增强瘦素敏感性导致体重减轻。此外,我们发现酵母中yPTP1的缺失完全消除了RA、cellstrol和withaferin A的延长寿命作用,而这些化合物显示出PTP1B抑制活性。此外,PTP1B敲低可以延长酵母和人类细胞的寿命,这表明PTP1B是调节细胞衰老的重要因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The natural product rotundic acid treats both aging and obesity by inhibiting PTP1B.

The occurrence of obesity is associated with age. But their interplay remains mysterious. Here, we discovered that rotundic acid (RA), a plant-derived pentacyclic triterpene, was a powerful agent for both anti-aging and treating obesity. Considering that obese individuals decrease the appetite-suppressing and energy-expenditure-enhancing functions of leptin leading to obesity, we found RA was a leptin sensitizer, evidenced by observations that RA enhanced the leptin sensitivity to normal diet-induced obese (DIO) mice, and had minimal or no use to normal lean mice, leptin receptor-deficient (db/db) mice, and leptin-deficient (ob/ob) mice. Simultaneously, RA significantly increased energy expenditure, BAT thermogenesis, and glucose metabolism in DIO mice, as the results of enhancing leptin sensitivity. Regarding mode of action, we demonstrated that RA is a noncompetitive inhibitor of leptin negative regulators protein tyrosine phosphatase 1B (PTP1B) and T-cell PTP through interaction with their C-terminus, thus leading to weight loss through enhancing leptin sensitivity. Besides, we showed that deletion of yPTP1 in yeast completely abolished the lifespan extension effect of RA, celstrol, and withaferin A, while these compounds exhibited PTP1B inhibition activity. Furthermore, PTP1B knockdown extend lifespan in yeast and human cells, indicating PTP1B is an important factor regulating cellular aging.

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