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Modulatory Effects of Caffeine and Pentoxifylline on Aromatic Antibiotics: A Role for Hetero-Complex Formation

Antimicrobial resistance is a major healthcare threat globally. Xanthines, including caffeine and pentoxifylline, are attractive candidates for drug repurposing, given their well-established safety and pharmacological profiles. This study aimed to analyze potential interactions between xanthines and...

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Autores principales: Woziwodzka, Anna, Krychowiak-Maśnicka, Marta, Gołuński, Grzegorz, Felberg, Anna, Borowik, Agnieszka, Wyrzykowski, Dariusz, Piosik, Jacek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8231999/
https://www.ncbi.nlm.nih.gov/pubmed/34198510
http://dx.doi.org/10.3390/molecules26123628
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author Woziwodzka, Anna
Krychowiak-Maśnicka, Marta
Gołuński, Grzegorz
Felberg, Anna
Borowik, Agnieszka
Wyrzykowski, Dariusz
Piosik, Jacek
author_facet Woziwodzka, Anna
Krychowiak-Maśnicka, Marta
Gołuński, Grzegorz
Felberg, Anna
Borowik, Agnieszka
Wyrzykowski, Dariusz
Piosik, Jacek
author_sort Woziwodzka, Anna
collection PubMed
description Antimicrobial resistance is a major healthcare threat globally. Xanthines, including caffeine and pentoxifylline, are attractive candidates for drug repurposing, given their well-established safety and pharmacological profiles. This study aimed to analyze potential interactions between xanthines and aromatic antibiotics (i.e., tetracycline and ciprofloxacin), and their impact on antibiotic antibacterial activity. UV-vis spectroscopy, statistical-thermodynamical modeling, and isothermal titration calorimetry were used to quantitatively evaluate xanthine-antibiotic interactions. The antibacterial profiles of xanthines, and xanthine-antibiotic mixtures, towards important human pathogens Staphylococcus aureus, Enterococcus faecium, Escherichia coli, Acinetobacter baumannii, Klebsiella pneumoniae, and Enterobacter cloacae were examined. Caffeine and pentoxifylline directly interact with ciprofloxacin and tetracycline, with neighborhood association constant values of 15.8–45.6 M(−1) and enthalpy change values up to −4 kJ·M(−1). Caffeine, used in mixtures with tested antibiotics, enhanced their antibacterial activity in most pathogens tested. However, antagonistic effects of caffeine were also observed, but only with ciprofloxacin toward Gram-positive pathogens. Xanthines interact with aromatic antibiotics at the molecular and in vitro antibacterial activity level. Given considerable exposure to caffeine and pentoxifylline, these interactions might be relevant for the effectiveness of antibacterial pharmacotherapy, and may help to identify optimal treatment regimens in the era of multidrug resistance.
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spelling pubmed-82319992021-06-26 Modulatory Effects of Caffeine and Pentoxifylline on Aromatic Antibiotics: A Role for Hetero-Complex Formation Woziwodzka, Anna Krychowiak-Maśnicka, Marta Gołuński, Grzegorz Felberg, Anna Borowik, Agnieszka Wyrzykowski, Dariusz Piosik, Jacek Molecules Article Antimicrobial resistance is a major healthcare threat globally. Xanthines, including caffeine and pentoxifylline, are attractive candidates for drug repurposing, given their well-established safety and pharmacological profiles. This study aimed to analyze potential interactions between xanthines and aromatic antibiotics (i.e., tetracycline and ciprofloxacin), and their impact on antibiotic antibacterial activity. UV-vis spectroscopy, statistical-thermodynamical modeling, and isothermal titration calorimetry were used to quantitatively evaluate xanthine-antibiotic interactions. The antibacterial profiles of xanthines, and xanthine-antibiotic mixtures, towards important human pathogens Staphylococcus aureus, Enterococcus faecium, Escherichia coli, Acinetobacter baumannii, Klebsiella pneumoniae, and Enterobacter cloacae were examined. Caffeine and pentoxifylline directly interact with ciprofloxacin and tetracycline, with neighborhood association constant values of 15.8–45.6 M(−1) and enthalpy change values up to −4 kJ·M(−1). Caffeine, used in mixtures with tested antibiotics, enhanced their antibacterial activity in most pathogens tested. However, antagonistic effects of caffeine were also observed, but only with ciprofloxacin toward Gram-positive pathogens. Xanthines interact with aromatic antibiotics at the molecular and in vitro antibacterial activity level. Given considerable exposure to caffeine and pentoxifylline, these interactions might be relevant for the effectiveness of antibacterial pharmacotherapy, and may help to identify optimal treatment regimens in the era of multidrug resistance. MDPI 2021-06-14 /pmc/articles/PMC8231999/ /pubmed/34198510 http://dx.doi.org/10.3390/molecules26123628 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Woziwodzka, Anna
Krychowiak-Maśnicka, Marta
Gołuński, Grzegorz
Felberg, Anna
Borowik, Agnieszka
Wyrzykowski, Dariusz
Piosik, Jacek
Modulatory Effects of Caffeine and Pentoxifylline on Aromatic Antibiotics: A Role for Hetero-Complex Formation
title Modulatory Effects of Caffeine and Pentoxifylline on Aromatic Antibiotics: A Role for Hetero-Complex Formation
title_full Modulatory Effects of Caffeine and Pentoxifylline on Aromatic Antibiotics: A Role for Hetero-Complex Formation
title_fullStr Modulatory Effects of Caffeine and Pentoxifylline on Aromatic Antibiotics: A Role for Hetero-Complex Formation
title_full_unstemmed Modulatory Effects of Caffeine and Pentoxifylline on Aromatic Antibiotics: A Role for Hetero-Complex Formation
title_short Modulatory Effects of Caffeine and Pentoxifylline on Aromatic Antibiotics: A Role for Hetero-Complex Formation
title_sort modulatory effects of caffeine and pentoxifylline on aromatic antibiotics: a role for hetero-complex formation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8231999/
https://www.ncbi.nlm.nih.gov/pubmed/34198510
http://dx.doi.org/10.3390/molecules26123628
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