Thrombosis Research Center, Department of Clinical Biochemistry and Immunohaematology, Faculty of Health Sciences, Interdisciplinary Excellence Research Program on Healthy Aging (PIEI-ES), Universidad de Talca, Talca, Chile.
Instituto de Química de Recursos Naturales, Programa de Investigación Asociativa en Cáncer Gástrico (PIA-CG), Universidad de Talca, Talca, Chile.
Biochem Pharmacol. 2018 Oct;156:215-222. doi: 10.1016/j.bcp.2018.08.035. Epub 2018 Aug 25.
Platelet mitochondrial dysfunction has been identified in different diseases. Platelet mitochondrial dysfunction favors platelet activation with a considerable increase in oxidative stress, which is implicated in platelet non-responsiveness to current antiplatelet therapy. The inhibition of platelet mitochondrial dysfunction could potentially be used as a new strategy for the development of antiplatelet activity drugs. In this context, we described quinone and hydroquinone derivatives and mitochondrially targeted compounds as initial precursors for the synthesis of new antiplatelet agents.
血小板线粒体功能障碍已在多种疾病中被发现。血小板线粒体功能障碍有利于血小板的激活,同时伴随着氧化应激的显著增加,这与血小板对当前抗血小板治疗的无反应性有关。抑制血小板线粒体功能障碍可能成为开发抗血小板活性药物的新策略。在这种情况下,我们将醌和氢醌衍生物以及靶向线粒体的化合物描述为合成新型抗血小板药物的初始前体。