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基于大黄酸的氮氧自由基衍生物作为靶向Keap1-Nrf2通路的潜在抗衰老剂的设计、合成与评价

Design, Synthesis, and Evaluation of Nitroxide Radical Derivatives Based on Rhein as Potential Anti-Aging Agents Targeting the Keap1-Nrf2 Pathway.

作者信息

Wang Jie, Peng Xuejing, Zhang Xinyue, Lin Jia, Zhang Qili, Li Jiaojiao, Cui Longchen, Zhao Lei

机构信息

College of Pharmacy, Gansu University of Chinese Medicine, Lanzhou, People's Republic of China.

Northwest Collaborative Innovation Center for Traditional Chinese Medicine Co-Constructed by Gansu Province & MOE of PRC, Gansu University of Chinese Medicine, Lanzhou, People's Republic of China.

出版信息

Drug Des Devel Ther. 2025 Jun 19;19:5153-5167. doi: 10.2147/DDDT.S516209. eCollection 2025.

Abstract

PURPOSE

Targeting the crucial Keap1-Nrf2-ARE antioxidant pathway, we selected Rhein - a natural anthraquinone from traditional Chinese medicine with established Keap1-Nrf2 inhibitory activity as our lead compound. Through rational structural modification by incorporating nitroxide radicals at the 3-carboxyl position, we aimed to develop enhanced Keap1-Nrf2 modulators with anti-aging potential.

PATIENTS AND METHODS

A series of rhein nitroxide derivatives were synthesized, and their free radical scavenging activity was assessed in vitro using DPPH and ABTS methods. Compound , demonstrating significant activity, was selected for further evaluation. Its effects on the survival of L02 hepatocytes under oxidative stress and the lifespan and stress tolerance of () were investigated. Additionally, the impacts of on antioxidant enzyme activity, malondialdehyde (MDA) levels, and reactive oxygen species (ROS) accumulation under oxidative stress were assessed. Molecular docking was conducted to analyze interactions between and the Kelch domain of Keap1.

RESULTS

Compound exhibited potent free radical scavenging activity, with IC values of 0.51 ± 0.09 mM against DPPH radicals and 0.12 ± 0.03 mM against ABTS radicals. It significantly improved the survival rate of L02 hepatocytes under oxidative stress, maintaining 95.42% viability ( < 0.01). In the model, extended the average lifespan and enhanced stress resistance, increasing GSH activity, reducing MDA content, and decreasing ROS accumulation. Molecular docking showed that penetrates deeply into the Kelch domain of Keap1, forming stable interactions with key residues.

CONCLUSION

Compound demonstrates superior antioxidant and anti-aging effects compared to the parent compound rhein, representing a highly promising anti-aging candidate and Keap1-Nrf2 signaling pathway modulator with potential as a novel therapeutic agent for age-related diseases.

摘要

目的

针对关键的Keap1-Nrf2-ARE抗氧化途径,我们选择了大黄酸——一种来自中药的天然蒽醌,其对Keap1-Nrf2具有已确定的抑制活性,作为我们的先导化合物。通过在3-羧基位置引入氮氧自由基进行合理的结构修饰,我们旨在开发具有抗衰老潜力的增强型Keap1-Nrf2调节剂。

患者和方法

合成了一系列大黄酸氮氧衍生物,并使用DPPH和ABTS方法在体外评估了它们的自由基清除活性。选择表现出显著活性的化合物 进行进一步评估。研究了其对氧化应激下L02肝细胞存活以及秀丽隐杆线虫()寿命和应激耐受性的影响。此外,评估了 在氧化应激下对抗氧化酶活性、丙二醛(MDA)水平和活性氧(ROS)积累的影响。进行分子对接以分析 与Keap1的Kelch结构域之间的相互作用。

结果

化合物 表现出强大的自由基清除活性,对DPPH自由基的IC值为0.51±0.09 mM,对ABTS自由基的IC值为0.12±0.03 mM。它显著提高了氧化应激下L02肝细胞的存活率,维持了95.42%的活力(<0.01)。在秀丽隐杆线虫模型中, 延长了平均寿命并增强了应激抵抗力,增加了谷胱甘肽(GSH)活性,降低了MDA含量,并减少了ROS积累。分子对接表明 深入穿透Keap1的Kelch结构域,与关键残基形成稳定相互作用。

结论

与母体化合物大黄酸相比,化合物 表现出优异的抗氧化和抗衰老作用,是一种极具潜力的抗衰老候选物和Keap1-Nrf2信号通路调节剂,有可能成为治疗与年龄相关疾病的新型治疗剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c62/12184699/f6a899c6167f/DDDT-19-5153-g0001.jpg

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