Department of Toxicology, School of Public Health, Peking University, Beijing, 100191, China.
Beijing Key Laboratory of Diagnostic and Traceability Technologies for Food Poisoning, Beijing Center for Disease Prevention and Control, Beijing Center of Preventive Medicine Research, Beijing, 100013, China.
Eur J Pharmacol. 2020 Dec 5;888:173558. doi: 10.1016/j.ejphar.2020.173558. Epub 2020 Sep 14.
Sappanone A (SA) is a homoisoflavonoid compound isolated from Caesalpinia sappan L. that selectively binds to inosine monophosphate dehydrogenase 2, a protein involved in aging. It is unknown if SA has an anti-aging effect and what is it mechanism. This study aimed to investigate the lifespan-extending and health-enhancing effects of SA, and the potential pharmacological mechanism in Caenorhabditis elegans (C. elegans). The worms were exposed to 0-50 μM SA. The effect on the lifespan was observed, and health status was evaluated by detecting motility, feeding, reproduction, thermotolerance, lipofuscin and ROS accumulation. To explore a possible mechanism, the transcription of the genes of the insulin/insulin-like growth factor-1 signalling pathway and heat stress response was detected by RT-qPCR. Moreover, subcellular distribution of green fluorescent protein-labeled DAF-16 was determined, and the interaction between SA and HSP-90 protein was simulated by molecular docking. We found that SA prolonged lifespan in C. elegans and enhanced motility and thermotolerance. The feeding and reproduction were not impacted. The ROS and lipofuscin accumulation was declined. Mechanistic study revealed that the gene expression levels of daf-16 and hsp-90 were up-regulated. Moreover, DAF-16 was translocated into the nucleus. SA was docked into the active pocket of HSP-90 in the simulation. SA (50 μM) can extend lifespan in C. elegans and decelerate aging by regulating the IIS pathway, and daf-16 is specifically important for the regulation of longevity. HSP-90 was involved in the enhancement of thermotolerance. Thus, SA may act as a promising candidate for the development of an anti-aging agent.
紫檀芪 A(SA)是从苏木(Caesalpinia sappan L.)中分离出的一种异黄酮类化合物,它选择性地结合到参与衰老的肌苷一磷酸脱氢酶 2(IMPDH2)上。目前尚不清楚 SA 是否具有抗衰老作用及其作用机制。本研究旨在探讨 SA 的延长寿命和增强健康的作用及其在秀丽隐杆线虫(C. elegans)中的潜在药理机制。将线虫暴露于 0-50μM 的 SA 中。观察其对线虫寿命的影响,并通过检测运动性、摄食、繁殖、耐热性、脂褐素和 ROS 积累来评估健康状况。为了探讨一种可能的机制,通过 RT-qPCR 检测胰岛素/胰岛素样生长因子-1 信号通路和热应激反应相关基因的转录。此外,通过荧光显微镜观察绿色荧光蛋白标记的 DAF-16 的亚细胞分布,并通过分子对接模拟 SA 与 HSP-90 蛋白的相互作用。我们发现 SA 可延长线虫的寿命并增强其运动性和耐热性。摄食和繁殖不受影响。ROS 和脂褐素的积累减少。机制研究表明,daf-16 和 hsp-90 的基因表达水平上调。此外,DAF-16 易位到细胞核中。SA 在模拟中与 HSP-90 的活性口袋结合。SA(50μM)可通过调节 IIS 通路延长线虫的寿命并延缓衰老,daf-16 对线虫寿命的调节具有特异性重要性。HSP-90 参与耐热性的增强。因此,SA 可能是开发抗衰老药物的有前途的候选药物。