Membranes (Nov 2021)

Study of Tissue-Specific Reactive Oxygen Species Formation by Cell Membrane Microarrays for the Characterization of Bioactive Compounds

  • Ane Elexpe,
  • Nerea Nieto,
  • Claudia Fernández-Cuétara,
  • Celtia Domínguez-Fernández,
  • Teresa Morera-Herreras,
  • María Torrecilla,
  • Cristina Miguélez,
  • Antonio Laso,
  • Eneko Ochoa,
  • María Bailen,
  • Azucena González-Coloma,
  • Iñigo Angulo-Barturen,
  • Egoitz Astigarraga,
  • Gabriel Barreda-Gómez

DOI
https://doi.org/10.3390/membranes11120943
Journal volume & issue
Vol. 11, no. 12
p. 943

Abstract

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The production of reactive oxygen species (ROS) increases considerably in situations of cellular stress, inducing lipid peroxidation and multiple alterations in proteins and nucleic acids. However, sensitivity to oxidative damage varies between organs and tissues depending on the triggering process. Certain drugs used in the treatment of diverse diseases such as malaria have side effects similar to those produced by oxidative damage, although no specific study has been conducted. For this purpose, cell membrane microarrays were developed and the superoxide production evoked by the mitochondrial activity was assayed in the presence of specific inhibitors: rotenone, antimycin A and azide. Once the protocol was set up on cell membrane isolated from rat brain areas, the effect of six antimalarial drugs (atovaquone, quinidine, doxycycline, mefloquine, artemisinin, and tafenoquine) and two essential oils (Rosmarinus officinalis and Origanum majoricum) were evaluated in multiple human samples. The basal activity was different depending on the type of tissue, the liver, jejunum and adrenal gland being the ones with the highest amount of superoxide. The antimalarial drugs studied showed specific behavior according to the type of human tissue analyzed, with atovaquone and quinidine producing the highest percentage of superoxide formation, and doxycycline the lowest. In conclusion, the analysis of superoxide production evaluated in cell membranes of a collection of human tissues allowed for the characterization of the safety profile of these antimalarial drugs against toxicity mediated by oxidative stress.

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