Literature DB >> 21190429

Direct visualization of phase separation induced by phenothiazine-type antipsychotic drugs in model lipid membranes.

Olga Wesołowska1, Krystyna Michalak, Andrzej B Hendrich.   

Abstract

Lipid rafts constitute dynamic assemblies within a bilayer, engaged in, e.g., signal transduction, membrane trafficking and cell polarization. Despite wide interest in the process of domain formation in binary or ternary lipid model systems, only a limited number of papers are devoted to the influence of different additives on this process. In particular, works devoted to the role of drugs in raft formation are missing. In the present study, the influence of trifluoperazine, thioridazine and chlorpromazine on domain organization in raft-mimicking model membranes was investigated. Using giant unilamellar vesicles formed from an equimolar DOPC:sphingomyelin:cholesterol mixture, we found that phenothiazines elevated the number of domains, decreased their area and markedly increased the total length of the domain border. The impact of studied drugs on phase separation in the raft lipid mixture was also confirmed by Laurdan generalized polarization measurements. Alteration of domain organization induced by antipsychotic drugs was very likely to arise from selective accumulation of phenothiazines in interfacial regions between liquid ordered and liquid disordered domains. Interpretation of the results allowed us to demonstrate new aspects underlaying mechanisms of action of phenothiazine-type antipsychotic drugs. To the best of our knowledge, this is the first report demonstrating the influence of drugs on domain morphology directly visualized in giant unilamellar vesicles.

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Year:  2010        PMID: 21190429     DOI: 10.3109/09687688.2010.533706

Source DB:  PubMed          Journal:  Mol Membr Biol        ISSN: 0968-7688            Impact factor:   2.857


  5 in total

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Authors:  Yong Zhou; Kwang-Jin Cho; Sarah J Plowman; John F Hancock
Journal:  J Biol Chem       Date:  2012-03-19       Impact factor: 5.157

2.  Cholesterol regulates prokaryotic Kir channel by direct binding to channel protein.

Authors:  Dev K Singh; Tzu-Pin Shentu; Decha Enkvetchakul; Irena Levitan
Journal:  Biochim Biophys Acta       Date:  2011-07-21

3.  Chemogenetic profiling reveals PP2A-independent cytotoxicity of proposed PP2A activators iHAP1 and DT-061.

Authors:  Gianmatteo Vit; Joana Duro; Girish Rajendraprasad; Emil P T Hertz; Lya Katrine Kauffeldt Holland; Melanie Bianca Weisser; Brennan C McEwan; Blanca Lopez-Mendez; Paula Sotelo-Parrilla; A Arockia Jeyaprakash; Guillermo Montoya; Niels Mailand; Kenji Maeda; Arminja Kettenbach; Marin Barisic; Jakob Nilsson
Journal:  EMBO J       Date:  2022-06-13       Impact factor: 14.012

4.  Phenothiazines inhibit hepatitis C virus entry, likely by increasing the fluidity of cholesterol-rich membranes.

Authors:  Ana M Chamoun-Emanuelli; Eve-Isabelle Pecheur; Rudo L Simeon; Da Huang; Paul S Cremer; Zhilei Chen
Journal:  Antimicrob Agents Chemother       Date:  2013-03-25       Impact factor: 5.191

5.  Effect of trifluoperazine on Tc-99m sestamibi uptake in patients with advanced nonsmall cell lung cancer.

Authors:  Ümmühan Abdülrezzak; Zeynep Erdoğan; Güler Silov; Ayşegül Özdal; Özgül Turhal
Journal:  Indian J Nucl Med       Date:  2016 Apr-Jun
  5 in total

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