姜黄素和肉桂酸(具有膜活性的天然酚类化合物)的共同线粒体靶标

IF 4.9 3区 医学 Q1 PHARMACOLOGY & PHARMACY
Tatiana A Fedotcheva, Natalia V Beloborodova, Nadezhda I Fedotcheva
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引用次数: 0

摘要

背景:研究表明,姜黄素对不同的细胞系统(包括酶和线粒体)具有多种作用。检测到的姜黄素对线粒体的作用多种多样,有保护作用,也有毒性作用。研究目的在本研究中,我们研究了姜黄素以及肉桂酸(姜黄素的微生物代谢产物和微生物分解姜黄素的可能产物)对离体线粒体的影响。研究方法使用选择性电极、荧光和光谱方法研究了膜电位、膨胀、呼吸和钙保持能力。结果研究发现,姜黄素在低浓度(10-20 μM)时可激活钙依赖性通透性转换孔(mPTP)的开放,并降低钙滞留能力和 mPTP 开放所需的阈值浓度。此外,姜黄素还能引起膜电位的浓度依赖性阶梯式下降,并伴随呼吸的激活和氧化磷酸化的降低,这表明姜黄素是一种典型的线粒体解偶联剂。解偶联效应在很大程度上取决于姜黄素的浓度,姜黄素的浓度也是逐步增加的,从 25 µM 时的微弱解偶联到 75-100 µM 时的完全解偶联。肉桂酸具有类似的效果,但去极化效果除外,其浓度要高出一个数量级。结论:据推测,姜黄素的解偶联作用是一种启动事件,可调节任何依赖能量和氧化还原的线粒体功能,从积极刺激到毒性紊乱。这种效应也可能是姜黄素诱导的不同细胞过程变化的基础,并可通过绕过微生物群,有针对性地将姜黄素输送到某些细胞来实现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Common Mitochondrial Targets of Curcumin and Cinnamic Acid, the Membrane-Active Natural Phenolic Compounds.

Background: Research has shown the multiple actions of curcumin on different cell systems, including enzymes and mitochondria. The detected effects of curcumin on mitochondria are diverse, ranging from protective to toxic. Objectives: In this present work, the influence of curcumin, as well as cinnamic acid, which is a microbial metabolite and a possible product of the microbial breakdown of curcumin, on isolated mitochondria, was investigated. Methods: Membrane potential, swelling, respiration, and calcium retention capacity were studied using selective electrodes, fluorescence and spectral methods. Results: It was found that curcumin at low concentrations (10-20 μM) activated the opening of the calcium-dependent permeability transition pore (mPTP) and decreased the calcium retention capacity and threshold concentrations necessary for the mPTP opening. Moreover, curcumin caused a concentration-dependent stepwise decrease in the membrane potential, accompanied by the activation of respiration and a decrease in oxidative phosphorylation, which indicates that curcumin is a typical mitochondrial uncoupler. The uncoupling effect strongly depended on the concentration of curcumin, which also increased, stepwise, from weak uncoupling at 25 µM to complete uncoupling at 75-100 µM. Cinnamic acid had similar effects, with the exception of the depolarizing effect, at concentrations that were an order of magnitude higher. Conclusions: Presumably, the uncoupling action of curcumin is a priming event that modulates any energy- and redox-dependent mitochondrial functions, from positive stimulation to toxic disorder. This effect can also underlie the curcumin-induced changes in different cellular processes and be achieved by targeted delivery of curcumin to certain cells, bypassing the microbiota.

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来源期刊
Pharmaceutics
Pharmaceutics Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
7.90
自引率
11.10%
发文量
2379
审稿时长
16.41 days
期刊介绍: Pharmaceutics (ISSN 1999-4923) is an open access journal which provides an advanced forum for the science and technology of pharmaceutics and biopharmaceutics. It publishes reviews, regular research papers, communications,  and short notes. Covered topics include pharmacokinetics, toxicokinetics, pharmacodynamics, pharmacogenetics and pharmacogenomics, and pharmaceutical formulation. Our aim is to encourage scientists to publish their experimental and theoretical details in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
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