缓解子痫前期线粒体氧化应激的二芳酰腙的研究进展

IF 6.8 1区 医学 Q1 CHEMISTRY, MEDICINAL
Maxim Mastyugin, R. Bernadett Vlocskó, Zsuzsanna K. Zsengellér, Béla Török* and Marianna Török*, 
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引用次数: 0

摘要

子痫前期是一种妊娠特异性综合征,与氧化应激有关,影响5-8%的妊娠,目前尚无有效治疗方法。在这里,二芳酰腙被设计、合成和研究作为线粒体靶向抗氧化剂,以减少胎盘氧化应激和减轻子痫前期症状。该设计基于密度泛函理论研究,揭示了具有nh基序的共轭电子结构似乎可以解释它们的作用。合成了30种化合物,并通过三种方法进行了测试,其中它们表现出优异的自由基清除活性,明显高于标准的Trolox。根据这些数据,我们选择了8种化合物进行基于细胞的检测。在人滋养细胞中诱导氧化应激,并以抗坏血酸和MitoTEMPO为标准评估化合物是否降低下游抗血管生成反应。水合腙预处理可减少h2o2暴露的滋养细胞线粒体超氧化物和sFLT-1的产生,表明这些化合物可以减轻线粒体氧化应激和抗血管生成反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Development of Diaryl Hydrazones for Alleviation of Mitochondrial Oxidative Stress in Preeclampsia

Development of Diaryl Hydrazones for Alleviation of Mitochondrial Oxidative Stress in Preeclampsia

Preeclampsia is a pregnancy-specific syndrome, linked to oxidative stress, affecting 5–8% of pregnancies, with no effective treatment available. Here, diaryl-hydrazones have been designed, synthesized, and investigated as mitochondria-targeting antioxidants to reduce placental oxidative stress and mitigate preeclampsia symptoms. The design, based on density functional theory studies, revealed that conjugated electron structure with the NH-motif appeared to explain their effect. Thirty compounds were synthesized and tested in three assays, where they exhibited excellent radical scavenging activity, significantly greater than that of the standard, Trolox. Based on the data, eight compounds were selected for cell-based assays. Oxidative stress was induced in human trophoblast cells and assessed whether the compounds reduced downstream antiangiogenic responses using ascorbic acid and MitoTEMPO as standards. The pretreatment with the hydrazones reduced mitochondrial superoxide and sFLT-1 production in H2O2-exposed trophoblast cells, indicating that mitochondrial oxidative stress and the anti-angiogenic response can be alleviated by these compounds.

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来源期刊
Journal of Medicinal Chemistry
Journal of Medicinal Chemistry 医学-医药化学
CiteScore
4.00
自引率
11.00%
发文量
804
审稿时长
1.9 months
期刊介绍: The Journal of Medicinal Chemistry is a prestigious biweekly peer-reviewed publication that focuses on the multifaceted field of medicinal chemistry. Since its inception in 1959 as the Journal of Medicinal and Pharmaceutical Chemistry, it has evolved to become a cornerstone in the dissemination of research findings related to the design, synthesis, and development of therapeutic agents. The Journal of Medicinal Chemistry is recognized for its significant impact in the scientific community, as evidenced by its 2022 impact factor of 7.3. This metric reflects the journal's influence and the importance of its content in shaping the future of drug discovery and development. The journal serves as a vital resource for chemists, pharmacologists, and other researchers interested in the molecular mechanisms of drug action and the optimization of therapeutic compounds.
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