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      Descending pathways from the superior colliculus mediating autonomic and respiratory effects associated with orienting behaviour

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          Abstract

          Abstract

          The ability to discriminate competing external stimuli and initiate contextually appropriate behaviours is a key brain function. Neurons in the deep superior colliculus (dSC) integrate multisensory inputs and activate descending projections to premotor pathways responsible for orienting, attention and defence, behaviours which involve adjustments to respiratory and cardiovascular parameters. However, the neural pathways that subserve the physiological components of orienting are poorly understood. We report that orienting responses to optogenetic dSC stimulation are accompanied by short‐latency autonomic, respiratory and electroencephalographic effects in awake rats, closely mimicking those evoked by naturalistic alerting stimuli. Physiological responses were not accompanied by detectable aversion or fear, and persisted under urethane anaesthesia, indicating independence from emotional stress. Anterograde and trans‐synaptic viral tracing identified a monosynaptic pathway that links the dSC to spinally projecting neurons in the medullary gigantocellular reticular nucleus (GiA), a key hub for the coordination of orienting and locomotor behaviours. In urethane‐anaesthetized animals, sympathoexcitatory and cardiovascular, but not respiratory, responses to dSC stimulation were replicated by optogenetic stimulation of the dSC–GiA terminals, suggesting a likely role for this pathway in mediating the autonomic components of dSC‐mediated responses. Similarly, extracellular recordings from putative GiA sympathetic premotor neurons confirmed short‐latency excitatory inputs from the dSC. This pathway represents a likely substrate for autonomic components of orienting responses that are mediated by dSC neurons and suggests a mechanism through which physiological and motor components of orienting behaviours may be integrated without the involvement of higher centres that mediate affective components of defensive responses.

          Key points

          • Neurons in the deep superior colliculus (dSC) integrate multimodal sensory signals to elicit context‐dependent innate behaviours that are accompanied by stereotypical cardiovascular and respiratory activities.

          • The pathways responsible for mediating the physiological components of colliculus‐mediated orienting behaviours are unknown. We show that optogenetic dSC stimulation evokes transient orienting, respiratory and autonomic effects in awake rats which persist under urethane anaesthesia.

          • Anterograde tracing from the dSC identified projections to spinally projecting neurons in the medullary gigantocellular reticular nucleus (GiA). Stimulation of this pathway recapitulated autonomic effects evoked by stimulation of dSC neurons.

          • Electrophysiological recordings from putative GiA sympathetic premotor neurons confirmed short latency excitatory input from dSC neurons.

          • This disynaptic dSC–GiA–spinal sympathoexcitatory pathway may underlie autonomic adjustments to salient environmental cues independent of input from higher centres.

          Abstract

          Abstract figure legend Salient acoustic and visual stimuli elicit stereotypical responses with motor, respiratory and cardiovascular components. Here we show that optogenetic stimulation of the deep caudolateral superior colliculus (SC) elicits orienting and arousal that is accompanied by tail vasoconstriction and increased respiratory activity in awake rats. Using a combination of electrophysiology in urethane‐anaesthetized rats and anterograde and trans‐synaptic viral tracing, we reveal a monosynaptic tecto‐medullary pathway from the superior colliculus to spinally projecting neurons in the gigantocellular reticular nucleus (GiA) that contributes to the sympathetic and cardiovascular components of SC responses. We propose that this pathway likely mediates components of innate motor and physiological responses to ecologically relevant naturalistic stimuli.

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          Most cited references82

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          Neural regulation of endocrine and autonomic stress responses.

          The survival and well-being of all species requires appropriate physiological responses to environmental and homeostatic challenges. The re- establishment and maintenance of homeostasis entails the coordinated activation and control of neuroendocrine and autonomic stress systems. These collective stress responses are mediated by largely overlapping circuits in the limbic forebrain, the hypothalamus and the brainstem, so that the respective contributions of the neuroendocrine and autonomic systems are tuned in accordance with stressor modality and intensity. Limbic regions that are responsible for regulating stress responses intersect with circuits that are responsible for memory and reward, providing a means to tailor the stress response with respect to prior experience and anticipated outcomes.
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            AAV-Mediated Anterograde Transsynaptic Tagging: Mapping Corticocollicular Input-Defined Neural Pathways for Defense Behaviors.

            To decipher neural circuits underlying brain functions, viral tracers are widely applied to map input and output connectivity of neuronal populations. Despite the successful application of retrograde transsynaptic viruses for identifying presynaptic neurons of transduced neurons, analogous anterograde transsynaptic tools for tagging postsynaptically targeted neurons remain under development. Here, we discovered that adeno-associated viruses (AAV1 and AAV9) exhibit anterograde transsynaptic spread properties. AAV1-Cre from transduced presynaptic neurons effectively and specifically drives Cre-dependent transgene expression in selected postsynaptic neuronal targets, thus allowing axonal tracing and functional manipulations of the latter input-defined neuronal population. Its application in superior colliculus (SC) reveals that SC neuron subpopulations receiving corticocollicular projections from auditory and visual cortex specifically drive flight and freezing, two different types of defense behavior, respectively. Together with an intersectional approach, AAV-mediated anterograde transsynaptic tagging can categorize neurons by their inputs and molecular identity, and allow forward screening of distinct functional neural pathways embedded in complex brain circuits.
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              The mammalian superior colliculus: laminar structure and connections.

              The superior colliculus is a laminated midbrain structure that acts as one of the centers organizing gaze movements. This review will concentrate on sensory and motor inputs to the superior colliculus, on its internal circuitry, and on its connections with other brainstem gaze centers, as well as its extensive outputs to those structures with which it is reciprocally connected. This will be done in the context of its laminar arrangement. Specifically, the superficial layers receive direct retinal input, and are primarily visual sensory in nature. They project upon the visual thalamus and pretectum to influence visual perception. These visual layers also project upon the deeper layers, which are both multimodal, and premotor in nature. Thus, the deep layers receive input from both somatosensory and auditory sources, as well as from the basal ganglia and cerebellum. Sensory, association, and motor areas of cerebral cortex provide another major source of collicular input, particularly in more encephalized species. For example, visual sensory cortex terminates superficially, while the eye fields target the deeper layers. The deeper layers are themselves the source of a major projection by way of the predorsal bundle which contributes collicular target information to the brainstem structures containing gaze-related burst neurons, and the spinal cord and medullary reticular formation regions that produce head turning.
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                Author and article information

                Contributors
                simon.mcmullan@mq.edu.au
                Journal
                J Physiol
                J Physiol
                10.1111/(ISSN)1469-7793
                TJP
                jphysiol
                The Journal of Physiology
                John Wiley and Sons Inc. (Hoboken )
                0022-3751
                1469-7793
                02 December 2022
                15 December 2022
                02 December 2022
                : 600
                : 24 ( doiID: 10.1113/tjp.v600.24 )
                : 5311-5332
                Affiliations
                [ 1 ] Macquarie Medical School Faculty of Medicine, Health & Human Sciences Macquarie University Sydney New South Wales Australia
                [ 2 ] Department of Physiology University of Melbourne Victoria Australia
                [ 3 ] School of Medical Sciences (Physiology) University of Sydney Sydney New South Wales Australia
                Author notes
                [*] [* ] Corresponding author Simon McMullan: Macquarie Medical School, Faculty of Medicine, Health & Human Sciences, Macquarie University, 75 Talavera Road, Sydney, NSW 2109, Australia.  Email: simon.mcmullan@ 123456mq.edu.au

                Author information
                https://orcid.org/0000-0002-6441-8794
                https://orcid.org/0000-0001-9580-3890
                https://orcid.org/0000-0002-6896-3298
                https://orcid.org/0000-0002-2183-5360
                https://orcid.org/0000-0001-6468-8922
                https://orcid.org/0000-0002-9754-8069
                https://orcid.org/0000-0003-1544-7924
                https://orcid.org/0000-0002-9854-1029
                Article
                TJP15328
                10.1113/JP283789
                10107157
                36271640
                0092006c-d8f2-4ad2-ad85-6af0f53300b7
                © 2022 The Authors. The Journal of Physiology published by John Wiley & Sons Ltd on behalf of The Physiological Society.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 30 August 2022
                : 14 October 2022
                Page count
                Figures: 11, Tables: 1, Pages: 22, Words: 12796
                Funding
                Funded by: National Health & Medical Research Council, Australia
                Award ID: APP2001128
                Award ID: APP1127817
                Funded by: Hillcrest Foundation
                Award ID: IPAP2018/0437
                Categories
                Research Article
                Neuroscience
                Editor's Choice
                Custom metadata
                2.0
                15 December 2022
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.2.7 mode:remove_FC converted:17.04.2023

                Human biology
                arousal,cardiovascular,innate behaviours,sensorimotor integration,sympathetic
                Human biology
                arousal, cardiovascular, innate behaviours, sensorimotor integration, sympathetic

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