Tauchen Jan, Huml Lukáš, Jurášek Michal, Regenstein Joe M, Ozogul Fatih
Department of Food Science, Faculty of Agrobiology, Food, and Natural Resources, Czech University of Life Sciences Prague, Kamýcká, Czechia.
Department of Chemistry of Natural Compounds, University of Chemistry and Technology Prague, Technická, Czechia.
Front Pharmacol. 2025 Jul 22;16:1599816. doi: 10.3389/fphar.2025.1599816. eCollection 2025.
Oxidative stress is recognized as both a causative and contributing factor in many human diseases. As a result, significant research has been devoted to the development of synthetic and semi-synthetic antioxidants (ATs). This review summarizes the therapeutic potential of synthetic ATs, explores their possible clinical applications, and highlights novel structural modifications aimed at improving their pharmacological properties. Additionally, it presents ideas for refining current antioxidant testing methodologies. Despite the ongoing research, the therapeutic efficacy of synthetic ATs remains ambiguous for several reasons. These include the following: therapeutic benefits resulting from non-antioxidant mechanisms, insufficient dosage to elicit an antioxidant effect, poor oral bioavailability, a narrow therapeutic index, or toxicity that precludes clinical use. Nevertheless, some compounds, such as ebselen, edaravone, MitoQ10, and potentially N-acetylcysteine, have shown promising results. However, further studies are needed to confirm their efficacy and clarify whether their therapeutic effects are truly mediated through antioxidant mechanisms. Dietary antioxidants have achieved relatively higher clinical success, although their toxicity has also led to the withdrawal of some agents. One emerging therapeutic strategy involves inhibition of NADPH oxidase (NOX) enzymatic activity, with compounds such as ebselen, S17834, and GKT137831 showing potential across various disease models. Efforts to enhance antioxidant properties through molecular modifications, using advanced technologies such as prodrug strategies, nanotechnology, polymer complexation, targeted delivery systems, or conversion into inhalable formulations, have yielded variable success. Still, confirming the clinical relevance of newly developed antioxidants will require a paradigm shift in the testing approaches. Future studies must better define the molecular context of antioxidant action, including the following: which biomolecules are being protected, the specific radical species targeted, the tissue and subcellular distribution of the antioxidant, and how levels of endogenous antioxidants and reactive oxygen species (ROS) change post-administration (e.g., within the mitochondria). Despite extensive research, only a few synthetic antioxidants, such as edaravone, are currently used in clinical practice. Currently, no new antioxidant drugs are expected to receive regulatory approval in the near future.
氧化应激被认为是许多人类疾病的致病因素和促成因素。因此,大量研究致力于合成和半合成抗氧化剂(ATs)的开发。本综述总结了合成ATs的治疗潜力,探讨了它们可能的临床应用,并强调了旨在改善其药理特性的新型结构修饰。此外,还提出了改进当前抗氧化剂测试方法的思路。尽管研究仍在进行,但由于多种原因,合成ATs的治疗效果仍不明确。这些原因包括:非抗氧化机制产生的治疗益处、引发抗氧化作用的剂量不足、口服生物利用度差、治疗指数窄或毒性妨碍临床使用。然而,一些化合物,如依布硒啉、依达拉奉、线粒体辅酶Q10以及可能的N-乙酰半胱氨酸,已显示出有前景的结果。然而,需要进一步研究来证实它们的疗效,并阐明其治疗效果是否真的通过抗氧化机制介导。膳食抗氧化剂在临床上取得了相对较高的成功,尽管它们的毒性也导致了一些药物的撤市。一种新兴的治疗策略涉及抑制NADPH氧化酶(NOX)的酶活性,依布硒啉、S17834和GKT137831等化合物在各种疾病模型中显示出潜力。通过分子修饰,利用前药策略、纳米技术、聚合物络合、靶向递送系统或转化为可吸入制剂等先进技术来增强抗氧化性能的努力取得了不同程度的成功。不过,要证实新开发的抗氧化剂的临床相关性,测试方法需要进行范式转变。未来的研究必须更好地界定抗氧化作用的分子背景,包括:哪些生物分子受到保护、靶向的特定自由基种类、抗氧化剂的组织和亚细胞分布,以及给药后内源性抗氧化剂和活性氧(ROS)水平如何变化(例如在线粒体内)。尽管进行了广泛研究,但目前临床实践中仅使用少数几种合成抗氧化剂,如依达拉奉。目前,预计近期不会有新的抗氧化剂药物获得监管批准。