In vivo photopharmacological inhibition of hippocampal activity via multimodal probes - perspective and opening steps on experimental and computational challenges.
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Abstract
Neurological conditions such as epilepsy can have a significant impact on people's lives. Here, we discuss a new perspective for the study/treatment of these conditions using photopharmacology. A multimodal, intracranial implant that incorporates fluidic channels for localised drug delivery, electrodes for recording and stimulation, and a light source for photoswitching is used for in vivo administration and deactivation of a photoresponsive AMPA antagonist. We review current advancements in the relevant disciplines and show experimentally that the inhibition of seizure-like events induced in the hippocampus by electrical stimulation can be altered upon switching the drug with light. We discuss the interconnection of the drug's photopharmacological properties with the design of the device by modelling light penetration into the rat brain with Monte Carlo simulations. This work delivers a new perspective, including initial experimental and computational efforts on in vivo photopharmacology to understand and eventually treat neurological conditions.
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Acknowledgements: The authors acknowledge Prof Stefan Hecht, Dr Michael Pätzel and Jutta Schwarz for reproducing the synthesis to provide photodrug 1. 3D data on the vascular system in the rat brain were kindly provided by Prof Hyung Joon Cho. The authors acknowledge Dr Dominik Marti for co-developing and maintaining MCmatlab. Furthermore, J.G. thanks Prof. Emil List-Kratochvil for the support and fruitful discussion, in particular, at the beginning of the project. J.G.'s special gratitude goes to Prof. Alexander Böker at the University of Potsdama and Fraunhofer IAPc, who gave space and support needed to work on his scientific vision as a Junior Group Leader. J.G. acknowledges the support from the German Research Foundation (Deutsche Forschungsgemeinschaft DFG via Research Fellowships Gz. GU 2073/1-1). A.C.L. acknowledges Welcome Trust for a Junior Interdisciplinary Fellowship. T.E.N. acknowledges funding from EPSRC Cambridge NanoDTC (EP/L015978/1). This work was funded by the EPSRC IRC in Targeted Delivery for Hard-to-Treat Cancers, EP/S009000/1. We gratefully acknowledge the fruitful discussions with the members of the Bioelectronics Laboratoryb.
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2050-7518
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Engineering and Physical Sciences Research Council (EP/S009000/1)

