Apostolova Nadezda, Victor Victor M
1 Faculty of Health Sciences, University Jaume I , Castellón de la Plana, Spain .
Antioxid Redox Signal. 2015 Mar 10;22(8):686-729. doi: 10.1089/ars.2014.5952.
Mitochondrial function and specifically its implication in cellular redox/oxidative balance is fundamental in controlling the life and death of cells, and has been implicated in a wide range of human pathologies. In this context, mitochondrial therapeutics, particularly those involving mitochondria-targeted antioxidants, have attracted increasing interest as potentially effective therapies for several human diseases. For the past 10 years, great progress has been made in the development and functional testing of molecules that specifically target mitochondria, and there has been special focus on compounds with antioxidant properties. In this review, we will discuss several such strategies, including molecules conjugated with lipophilic cations (e.g., triphenylphosphonium) or rhodamine, conjugates of plant alkaloids, amino-acid- and peptide-based compounds, and liposomes. This area has several major challenges that need to be confronted. Apart from antioxidants and other redox active molecules, current research aims at developing compounds that are capable of modulating other mitochondria-controlled processes, such as apoptosis and autophagy. Multiple chemically different molecular strategies have been developed as delivery tools that offer broad opportunities for mitochondrial manipulation. Additional studies, and particularly in vivo approaches under physiologically relevant conditions, are necessary to confirm the clinical usefulness of these molecules.
线粒体功能,特别是其在细胞氧化还原/氧化平衡中的作用,对于控制细胞的生死至关重要,并且与多种人类疾病相关。在此背景下,线粒体疗法,尤其是那些涉及线粒体靶向抗氧化剂的疗法,作为治疗多种人类疾病的潜在有效疗法,已引起越来越多的关注。在过去的10年里,在特异性靶向线粒体的分子的开发和功能测试方面取得了巨大进展,并且特别关注具有抗氧化特性的化合物。在这篇综述中,我们将讨论几种这样的策略,包括与亲脂性阳离子(如三苯基膦)或罗丹明共轭的分子、植物生物碱共轭物、基于氨基酸和肽的化合物以及脂质体。该领域存在几个需要面对的重大挑战。除了抗氧化剂和其他氧化还原活性分子外,当前的研究旨在开发能够调节其他线粒体控制过程的化合物,如细胞凋亡和自噬。已经开发了多种化学性质不同的分子策略作为递送工具,为线粒体操作提供了广泛的机会。需要进行更多的研究,特别是在生理相关条件下的体内研究,以证实这些分子的临床实用性。