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      Brainwide Projections of Mouse Dopaminergic Zona Incerta Neurons

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          ABSTRACT

          The zona incerta (ZI) supports diverse behaviors including binge feeding, sleep–wake cycles, nociception, and hunting. Diverse ZI functions can be attributed to its heterogeneous neurochemical characterization, cytoarchitecture, and efferent connections. The ZI is predominantly GABAergic, but we recently identified a subset of medial ZI GABA cells that are marked by the enzyme tyrosine hydroxylase (TH) and produce dopamine (DA). While the role of GABA within the ZI is well studied, less is known about the functions of ZI DA cells. To identify potential roles of ZI DA cells, we further phenotyped them and mapped their efferent fiber projections. We showed that wild‐type TH‐immunoreactive (‐ir) ZI cells did not express somatostatin or calretinin immunoreactivity. We next validated a Th‐cre;L10‐Egfp mouse line and found that medial Egfp ZI cells were more likely to be TH‐ir. We therefore delivered a Cre‐dependent virus into the medial ZI of Th‐cre or Th‐cre;L10‐Egfp mice and selected two injection cases for full brain mapping, namely, cases with the lowest and highest colocalization between TH‐ir and virally transduced, DsRed‐labeled cells, to identify common target sites. Overall, DsRed‐labeled fibers were distributed brainwide and were most prominent within the motor‐related midbrain (MBmot), notably the periaqueductal gray area and superior colliculus. We also observed numerous DsRed‐labeled fibers within the polymodal association cortex‐related thalamus (DORpm), like paraventricular thalamic nucleus and nucleus of reunions, that processes external and internal sensory input. Overall, ZI DA cells displayed a similar fiber profile to ZI GABA cells and may integrate sensory input to coordinate motor output at their target sites.

          Abstract

          Cre‐dependent viral tracing from medial dopaminergic ZI neurons revealed abundant fiber projections rostrocaudally throughout the brain. Interestingly, the midbrain motor regions, including the periaqueductal gray area and superior colliculus, contained the densest accumulation of fiber projections, and this fiber density was independent of the region size.

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          The Allen Mouse Brain Common Coordinate Framework: A 3D Reference Atlas

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            Dopamine in motivational control: rewarding, aversive, and alerting.

            Midbrain dopamine neurons are well known for their strong responses to rewards and their critical role in positive motivation. It has become increasingly clear, however, that dopamine neurons also transmit signals related to salient but nonrewarding experiences such as aversive and alerting events. Here we review recent advances in understanding the reward and nonreward functions of dopamine. Based on this data, we propose that dopamine neurons come in multiple types that are connected with distinct brain networks and have distinct roles in motivational control. Some dopamine neurons encode motivational value, supporting brain networks for seeking, evaluation, and value learning. Others encode motivational salience, supporting brain networks for orienting, cognition, and general motivation. Both types of dopamine neurons are augmented by an alerting signal involved in rapid detection of potentially important sensory cues. We hypothesize that these dopaminergic pathways for value, salience, and alerting cooperate to support adaptive behavior. Copyright © 2010 Elsevier Inc. All rights reserved.
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              A synaptic threshold mechanism for computing escape decisions

              Escaping from imminent danger is an instinctive behaviour fundamental for survival that requires classifying sensory stimuli as harmless or threatening. The absence of threat allows animals to forage for essential resources, but as the level of threat and potential for harm increases, they have to decide whether or not to seek safety1. Despite previous work on instinctive defensive behaviours in rodents2–11, little is known about how the brain computes the threat level for initiating escape. Here we show that the probability and vigour of escape in mice scale with the saliency of innate threats, and are well described by a model that computes the distance between threat level and an escape threshold. Calcium imaging and optogenetics in the midbrain of freely behaving mice show that the activity of excitatory neurons in the deep layers of the medial superior colliculus (mSC) represents the threat stimulus saliency and is predictive of escape, whereas dorsal periaqueductal gray (dPAG) glutamatergic neurons encode exclusively the escape choice and control escape vigour. We demonstrate a feed-forward monosynaptic excitatory connection from mSC to dPAG neurons that is weak and unreliable – yet necessary for escape behaviour – which provides a synaptic threshold for dPAG activation and the initiation of escape. This threshold can be overcome by high mSC network activity because of short-term synaptic facilitation and recurrent excitation within the mSC, which amplifies and sustains synaptic drive to the dPAG. Thus, dPAG glutamatergic neurons compute escape decisions and vigour using a synaptic mechanism to threshold threat information received from the mSC, and provide a biophysical model of how the brain performs a critical behavioural computation.
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                Author and article information

                Contributors
                biancabono@cmail.carleton.ca
                melissa.chee@carleton.ca
                Journal
                J Comp Neurol
                J Comp Neurol
                10.1002/(ISSN)1096-9861
                CNE
                The Journal of Comparative Neurology
                John Wiley and Sons Inc. (Hoboken )
                0021-9967
                1096-9861
                16 March 2025
                March 2025
                : 533
                : 3 ( doiID: 10.1002/cne.v533.3 )
                : e70039
                Affiliations
                [ 1 ] Department of Neuroscience Carleton University Ottawa Ontario Canada
                [ 2 ] Department of Biological Sciences The University of Texas at El Paso El Paso Texas USA
                [ 3 ] Border Biomedical Research Center The University of Texas at El Paso El Paso Texas USA
                Author notes
                [*] [* ] Correspondence: Bianca S. Bono ( biancabono@ 123456cmail.carleton.ca ) | Melissa J. Chee ( melissa.chee@ 123456carleton.ca )

                Author information
                https://orcid.org/0000-0002-5078-9682
                https://orcid.org/0000-0001-8283-9202
                https://orcid.org/0009-0008-8368-7827
                https://orcid.org/0009-0004-0764-0964
                https://orcid.org/0000-0003-0254-3546
                https://orcid.org/0000-0003-3815-9095
                Article
                CNE70039
                10.1002/cne.70039
                11911292
                40090880
                d26e990f-c4b6-4248-84e1-0c492d5fd2cb
                © 2025 The Author(s). The Journal of Comparative Neurology published by Wiley Periodicals LLC.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 27 January 2025
                : 16 September 2024
                : 24 February 2025
                Page count
                Figures: 17, Tables: 5, Pages: 34, Words: 15375
                Funding
                Funded by: Queen Elizabeth II Graduate Scholarship in Science and Technology
                Funded by: Carleton University Work Study Program
                Funded by: Howard Hughes Medical Institute education grant 52008125
                Funded by: Internship‐Carleton University Research experience for Undergraduate Students
                Funded by: UTEP PERSIST Brain Mapping & Connectomics Laboratory
                Funded by: National Science Foundation , doi 10.13039/100000001;
                Award ID: DUE‐1565063
                Funded by: Eloise E. and Patrick Wieland Fellowship
                Funded by: Natural Sciences and Engineering Research Council of Canada , doi 10.13039/501100000038;
                Award ID: Canadian Graduate Scholarship ‐ Doctoral program
                Award ID: Canadian Graduate Scholarship ‐ Master's program
                Award ID: RGPIN‐2017‐06272
                Funded by: National Institutes of Health , doi 10.13039/100000002;
                Award ID: SC1GM12721
                Categories
                Research Article
                Research Article
                Custom metadata
                2.0
                March 2025
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.5.4 mode:remove_FC converted:16.03.2025

                Neurology
                calretinin,dopamine,fibers,gaba,hypothalamus,midbrain,somatostatin,thalamus,tracing,ab_2201528,ab_10013483,ab_11177031,ab_2340593,ab_2315778,ab_10846469,ab_2302603,ab_11180865,ab_141362,ab_2571567,ab_2536611,ab_2910635,ab_2313568,ab_2313737,scr_016477,imsr_jax:000664

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