Rouco Lara, Alvariño Rebeca, Alfonso Amparo, Fernández-Fariña Sandra, González-Noya Ana M, Martínez-Calvo Miguel, Pedrido Rosa, Rodríguez-Silva Laura, Maneiro Marcelino
Departamento de Química Inorgánica, Facultade de Ciencias, Campus Terra, Universidade de Santiago de Compostela, 27002 Lugo, Spain.
Departamento de Fisiología, Facultade de Veterinaria, IDIS, Universidade de Santiago de Compostela, 27002 Lugo, Spain.
Antioxidants (Basel). 2024 Feb 22;13(3):265. doi: 10.3390/antiox13030265.
Manganosalen complexes are a class of catalytic antioxidants with beneficial effects against different neurological disorders according to various in vitro and in vivo studies. The interest in the factors that determine their antioxidant activity is based on the fact that they are key to achieving more efficient models. In this work, we report a set of new manganosalen complexes, thoroughly characterized in the solid state and in solution by different techniques. The chelating Schiff base ligands used were prepared from condensation of different substituted hydroxybenzaldehydes with 1,2-diaminoethane and 1,3-diaminopropane. The antioxidant activity of the new models was tested through superoxide dismutase and catalase probes in conjunction with the studies about their neuroprotective effects in human SH-SY5Y neuroblastoma cells in an oxidative stress model. The ability to scavenge excess reactive oxygen species (ROS) varied depending on the manganosalen models, which also yielded different improvements in cell survival. An assessment of the different factors that affect the oxidant activity for these complexes, and others previously reported, revealed the major influence of the structural factors versus the redox properties of the manganosalen complexes.
根据各种体外和体内研究,锰-salen配合物是一类具有催化抗氧化活性的物质,对不同的神经疾病具有有益作用。对决定其抗氧化活性的因素的关注基于这样一个事实,即它们是实现更高效模型的关键。在这项工作中,我们报道了一组新的锰-salen配合物,通过不同技术对其固态和溶液状态进行了全面表征。所使用的螯合席夫碱配体是由不同取代的羟基苯甲醛与1,2-二氨基乙烷和1,3-二氨基丙烷缩合制备而成。通过超氧化物歧化酶和过氧化氢酶探针测试了新模型的抗氧化活性,并结合在氧化应激模型中对其在人SH-SY5Y神经母细胞瘤细胞中的神经保护作用的研究。清除过量活性氧(ROS)的能力因锰-salen模型而异,这也导致细胞存活率有不同程度的提高。对影响这些配合物以及先前报道的其他配合物氧化活性的不同因素的评估表明,结构因素对锰-salen配合物的氧化还原性质具有主要影响。