Illuminating phenylazopyridines to photoswitch metabotropic glutamate receptors

Phenylazopyridines are photoisomerizable compounds with high potential to control biological functions with light. We have obtained a series of phenylazopyridines with light dependent activity as negative allosteric modulators (NAM) of metabotropic glutamate receptor subtype 5 (mGlu). Here we descri...

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Detalles Bibliográficos
Autores: Gómez-Santacana, Xavier|||0000-0001-8830-0494, Pittolo, Silvia|||0000-0002-5673-1692, Rovira, Xavier|||0000-0002-9764-9927, Lopez, Marc, Zussy, Charleine, Dalton, James A. R.|||0000-0002-5279-4581, Faucherre, Adèle, Jopling, Chris, Pin, Jean-Philippe|||0000-0002-1423-345X, Ciruela, Francisco|||0000-0003-0832-3739, Goudet, Cyril|||0000-0002-8255-3535, Giraldo, Jesús|||0000-0001-7082-4695, Gorostiza, Pau|||0000-0002-7268-5577, Llebaria, Amadeu|||0000-0002-8200-4827
Tipo de recurso: artículo
Fecha de publicación:2017
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:186140
Acceso en línea:https://ddd.uab.cat/record/186140
https://dx.doi.org/urn:doi:10.1021/acscentsci.6b00353
Access Level:acceso abierto
Descripción
Sumario:Phenylazopyridines are photoisomerizable compounds with high potential to control biological functions with light. We have obtained a series of phenylazopyridines with light dependent activity as negative allosteric modulators (NAM) of metabotropic glutamate receptor subtype 5 (mGlu). Here we describe the factors needed to achieve an operational molecular photoisomerization and its effective translation into in vitro and in vivo receptor photoswitching, which includes zebrafish larva motility and the regulation of the antinociceptive effects in mice. The combination of light and some specific phenylazopyridine ligands displays atypical pharmacological profiles, including light-dependent receptor overactivation, which can be observed both in vitro and in vivo. Remarkably, the localized administration of light and a photoswitchable compound in the peripheral tissues of rodents or in the brain amygdalae results in an illumination-dependent analgesic effect. The results reveal a robust translation of the phenylazopyridine photoisomerization to a precise photoregulation of biological activity. The cis - trans photoisomerization of phenylazopyridines, allowing mGlu receptor activity photoswitching in cells, is used in vivo to control zebrafish motility with light and analgesia in mice including peripheral and brain localized illumination.