Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/43388
Title: Coreleased orexin and glutamate evoke nonredundant spike outputs and computations in histamine neurons
Authors: Schöne, C
Apergis-Schoute, J
Sakurai, T
Adamantidis, A
Burdakov, D
First Published: 24-Apr-2014
Publisher: Elsevier
Citation: Cell Rep, 2014, 7 (3), pp. 697-704
Abstract: Stable wakefulness requires orexin/hypocretin neurons (OHNs) and OHR2 receptors. OHNs sense diverse environmental cues and control arousal accordingly. For unknown reasons, OHNs contain multiple excitatory transmitters, including OH peptides and glutamate. To analyze their cotransmission within computational frameworks for control, we optogenetically stimulated OHNs and examined resulting outputs (spike patterns) in a downstream arousal regulator, the histamine neurons (HANs). OHR2s were essential for sustained HAN outputs. OHR2-dependent HAN output increased linearly during constant OHN input, suggesting that the OHN→HAN(OHR2) module may function as an integral controller. OHN stimulation evoked OHR2-dependent slow postsynaptic currents, similar to midnanomolar OH concentrations. Conversely, glutamate-dependent output transiently communicated OHN input onset, peaking rapidly then decaying alongside OHN→HAN glutamate currents. Blocking glutamate-driven spiking did not affect OH-driven spiking and vice versa, suggesting isolation (low cross-modulation) of outputs. Therefore, in arousal regulators, cotransmitters may translate distinct features of OHN activity into parallel, nonredundant control signals for downstream effectors.
DOI Link: 10.1016/j.celrep.2014.03.055
eISSN: 2211-1247
Links: https://www.sciencedirect.com/science/article/pii/S2211124714002526?via%3Dihub
http://hdl.handle.net/2381/43388
Version: Publisher Version
Status: Peer-reviewed
Type: Journal Article
Rights: Copyright © the authors, 2014. This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Appears in Collections:Published Articles, Dept. of Neuroscience, Psychology and Behaviour

Files in This Item:
File Description SizeFormat 
1-s2.0-S2211124714002526-main.pdfPublished (publisher PDF)8.74 MBAdobe PDFView/Open


Items in LRA are protected by copyright, with all rights reserved, unless otherwise indicated.