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Ex Vivo Feedback Control of Neurotransmission Using a Photocaged Adenosine A1 Receptor Agonist
We report the design, synthesis, and validation of the novel compound photocaged N(6)-cyclopentyladenosine (cCPA) to achieve precisely localized and timed release of the parent adenosine A1 receptor agonist CPA using 405 nm light. G(i) protein-coupled A(1) receptors (A(1)Rs) modulate neurotransmissi...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9408941/ https://www.ncbi.nlm.nih.gov/pubmed/36012151 http://dx.doi.org/10.3390/ijms23168887 |
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author | Craey, Erine Hulpia, Fabian Spanoghe, Jeroen Manzella, Simona Larsen, Lars E. Sprengers, Mathieu De Bundel, Dimitri Smolders, Ilse Carrette, Evelien Delbeke, Jean Vonck, Kristl Boon, Paul Van Calenbergh, Serge Wadman, Wytse J. Raedt, Robrecht |
author_facet | Craey, Erine Hulpia, Fabian Spanoghe, Jeroen Manzella, Simona Larsen, Lars E. Sprengers, Mathieu De Bundel, Dimitri Smolders, Ilse Carrette, Evelien Delbeke, Jean Vonck, Kristl Boon, Paul Van Calenbergh, Serge Wadman, Wytse J. Raedt, Robrecht |
author_sort | Craey, Erine |
collection | PubMed |
description | We report the design, synthesis, and validation of the novel compound photocaged N(6)-cyclopentyladenosine (cCPA) to achieve precisely localized and timed release of the parent adenosine A1 receptor agonist CPA using 405 nm light. G(i) protein-coupled A(1) receptors (A(1)Rs) modulate neurotransmission via pre- and post-synaptic routes. The dynamics of the CPA-mediated effect on neurotransmission, characterized by fast activation and slow recovery, make it possible to implement a closed-loop control paradigm. The strength of neurotransmission is monitored as the amplitude of stimulus-evoked local field potentials. It is used for feedback control of light to release CPA. This system makes it possible to regulate neurotransmission to a pre-defined level in acute hippocampal brain slices incubated with 3 µM cCPA. This novel approach of closed-loop photopharmacology holds therapeutic potential for fine-tuned control of neurotransmission in diseases associated with neuronal hyperexcitability. |
format | Online Article Text |
id | pubmed-9408941 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-94089412022-08-26 Ex Vivo Feedback Control of Neurotransmission Using a Photocaged Adenosine A1 Receptor Agonist Craey, Erine Hulpia, Fabian Spanoghe, Jeroen Manzella, Simona Larsen, Lars E. Sprengers, Mathieu De Bundel, Dimitri Smolders, Ilse Carrette, Evelien Delbeke, Jean Vonck, Kristl Boon, Paul Van Calenbergh, Serge Wadman, Wytse J. Raedt, Robrecht Int J Mol Sci Communication We report the design, synthesis, and validation of the novel compound photocaged N(6)-cyclopentyladenosine (cCPA) to achieve precisely localized and timed release of the parent adenosine A1 receptor agonist CPA using 405 nm light. G(i) protein-coupled A(1) receptors (A(1)Rs) modulate neurotransmission via pre- and post-synaptic routes. The dynamics of the CPA-mediated effect on neurotransmission, characterized by fast activation and slow recovery, make it possible to implement a closed-loop control paradigm. The strength of neurotransmission is monitored as the amplitude of stimulus-evoked local field potentials. It is used for feedback control of light to release CPA. This system makes it possible to regulate neurotransmission to a pre-defined level in acute hippocampal brain slices incubated with 3 µM cCPA. This novel approach of closed-loop photopharmacology holds therapeutic potential for fine-tuned control of neurotransmission in diseases associated with neuronal hyperexcitability. MDPI 2022-08-10 /pmc/articles/PMC9408941/ /pubmed/36012151 http://dx.doi.org/10.3390/ijms23168887 Text en © 2022 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 | Communication Craey, Erine Hulpia, Fabian Spanoghe, Jeroen Manzella, Simona Larsen, Lars E. Sprengers, Mathieu De Bundel, Dimitri Smolders, Ilse Carrette, Evelien Delbeke, Jean Vonck, Kristl Boon, Paul Van Calenbergh, Serge Wadman, Wytse J. Raedt, Robrecht Ex Vivo Feedback Control of Neurotransmission Using a Photocaged Adenosine A1 Receptor Agonist |
title | Ex Vivo Feedback Control of Neurotransmission Using a Photocaged Adenosine A1 Receptor Agonist |
title_full | Ex Vivo Feedback Control of Neurotransmission Using a Photocaged Adenosine A1 Receptor Agonist |
title_fullStr | Ex Vivo Feedback Control of Neurotransmission Using a Photocaged Adenosine A1 Receptor Agonist |
title_full_unstemmed | Ex Vivo Feedback Control of Neurotransmission Using a Photocaged Adenosine A1 Receptor Agonist |
title_short | Ex Vivo Feedback Control of Neurotransmission Using a Photocaged Adenosine A1 Receptor Agonist |
title_sort | ex vivo feedback control of neurotransmission using a photocaged adenosine a1 receptor agonist |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9408941/ https://www.ncbi.nlm.nih.gov/pubmed/36012151 http://dx.doi.org/10.3390/ijms23168887 |
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