Cyclodextrins Exert a Ligand-like Current Inhibitory Effect on the K

KV1.3 cholesterol cyclodextrin ligand-like interaction membrane fluidity membrane hydration membrane lipid order

Journal

Frontiers in molecular biosciences
ISSN: 2296-889X
Titre abrégé: Front Mol Biosci
Pays: Switzerland
ID NLM: 101653173

Informations de publication

Date de publication:
2021
Historique:
received: 02 07 2021
accepted: 19 10 2021
entrez: 22 11 2021
pubmed: 23 11 2021
medline: 23 11 2021
Statut: epublish

Résumé

Cyclodextrins (CDs) are cyclic oligosaccharides capable of forming water-soluble complexes with a variety of otherwise poorly soluble molecules including cholesterol and different drugs. Consistently, CDs are widely used in research and clinical practice to deplete cholesterol from cellular membranes or to increase solubility and bioavailability of different pharmaceuticals at local concentrations in the millimolar range. Effects of CDs exerted on cellular functions are generally thought to originate from reductions in cholesterol levels. Potential direct, ligand-like CD effects are largely neglected in spite of several recent studies reporting direct interaction between CDs and proteins including AMP-activated protein kinase, β-amyloid peptides, and α-synuclein. In this study, by using patch-clamp technique, time-resolved quantitation of cholesterol levels and biophysical parameters and applying cholesterol-extracting and non-cholesterol-extracting CDs at 1 and 5 mM concentrations, we provide evidence for a previously unexplored ligand-like, cholesterol-independent current inhibitory effect of CDs on K

Identifiants

pubmed: 34805269
doi: 10.3389/fmolb.2021.735357
pii: 735357
pmc: PMC8599428
doi:

Types de publication

Journal Article

Langues

eng

Pagination

735357

Informations de copyright

Copyright © 2021 Kovacs, Sohajda, Szente, Nagy, Panyi, Varga and Zakany.

Déclaration de conflit d'intérêts

TS and LS was employed by the CycloLab Cyclodextrin R and D Laboratory Ltd. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Tamas Kovacs (T)

Division of Biophysics, Department of Biophysics and Cell Biology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.

Tamas Sohajda (T)

CycloLab Cyclodextrin R and D Laboratory Ltd., Budapest, Hungary.

Lajos Szente (L)

CycloLab Cyclodextrin R and D Laboratory Ltd., Budapest, Hungary.

Peter Nagy (P)

Division of Biophysics, Department of Biophysics and Cell Biology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.

Gyorgy Panyi (G)

Division of Biophysics, Department of Biophysics and Cell Biology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.

Zoltan Varga (Z)

Division of Biophysics, Department of Biophysics and Cell Biology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.

Florina Zakany (F)

Division of Biophysics, Department of Biophysics and Cell Biology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.

Classifications MeSH