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@ARTICLE{Maleeva:864468,
author = {Maleeva, Galyna and Wutz, Daniel and Rustler, Karin and
Nin‐Hill, Alba and Petukhova, Elena and
Bautista‐Barrufet, Antoni and Gomila‐Juaneda, Alexandre
and Scholze, Petra and Peiretti, Franck and Rovira, Carme
and König, Burkhard and Gorostiza, Pau and Bregestovski,
Piotr and Alfonso-Prieto, Mercedes},
title = {{A} photoswitchable {GABA} receptor channel blocker},
journal = {British journal of pharmacology},
volume = {176},
number = {15},
issn = {1476-5381},
address = {Malden, MA},
publisher = {Wiley},
reportid = {FZJ-2019-04249},
pages = {2661-2677},
year = {2019},
abstract = {Background and PurposeAnion‐selective Cys‐loop
receptors (GABA and glycine receptors) provide the main
inhibitory drive in the CNS. Both types of receptor operate
via chloride‐selective ion channels, though with different
kinetics, pharmacological profiles, and localization.
Disequilibrium in their function leads to a variety of
disorders, which are often treated with allosteric
modulators. The few available GABA and glycine receptor
channel blockers effectively suppress inhibitory currents in
neurons, but their systemic administration is highly toxic.
With the aim of developing an efficient light‐controllable
modulator of GABA receptors, we constructed
azobenzene‐nitrazepam (Azo‐NZ1), which is composed of a
nitrazepam moiety merged to an azobenzene photoisomerizable
group.Experimental ApproachThe experiments were carried out
on cultured cells expressing Cys‐loop receptors of known
subunit composition and in brain slices using patch‐clamp.
Site‐directed mutagenesis and molecular modelling
approaches were applied to evaluate the mechanism of action
of Azo‐NZ1.Key ResultsAt visible light, being in
trans‐configuration, Azo‐NZ1 blocked heteromeric
α1/β2/γ2 GABAA receptors, ρ2 GABAA (GABAC), and α2
glycine receptors, whereas switching the compound into
cis‐state by UV illumination restored the activity.
Azo‐NZ1 successfully photomodulated GABAergic currents
recorded from dentate gyrus neurons. We demonstrated that in
trans‐configuration, Azo‐NZ1 blocks the Cl‐selective
ion pore of GABA receptors interacting mainly with the 2′
level of the TM2 region.Conclusions and
ImplicationsAzo‐NZ1 is a soluble light‐driven
Cl‐channel blocker, which allows photo‐modulation of the
activity induced by anion‐selective Cys‐loop receptors.
Azo‐NZ1 is able to control GABAergic postsynaptic currents
and provides new opportunities to study inhibitory
neurotransmission using patterned illumination.},
cin = {IAS-5 / INM-9},
ddc = {610},
cid = {I:(DE-Juel1)IAS-5-20120330 / I:(DE-Juel1)INM-9-20140121},
pnm = {571 - Connectivity and Activity (POF3-571) / 574 - Theory,
modelling and simulation (POF3-574)},
pid = {G:(DE-HGF)POF3-571 / G:(DE-HGF)POF3-574},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:30981211},
UT = {WOS:000474034600001},
doi = {10.1111/bph.14689},
url = {https://juser.fz-juelich.de/record/864468},
}