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      A Subregion of Insular Cortex Is Required for Rapid Taste-Visceral Integration and Consequent Conditioned Taste Aversion and Avoidance Expression in Rats

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          Abstract

          Postingestive signals are important for shaping appetitive and consummatory responses, but the brain mechanisms required to assimilate interoceptive events with those at the frontlines of ingestion (taste-guided) are poorly understood. Here, we investigated whether an insular cortex (IC) region, which receives viscerosensory input, including gustatory, is required to modify taste-elicited consummatory reactions in response to a real-time interoceptive change using a serial taste reactivity (TR) test where the rats’ oromotor and somatic reactions to intraoral (IO) infusions of sucrose were periodically assessed over 45 min following lithium chloride (LiCl) administration. Results showed that neurally-intact rats shifted from an ingestive repertoire to an aversive one as LiCl took effect. Overall, this hedonic shift was delayed in rats with bilateral neurotoxic IC lesions. Rats with greater neuronal loss in posterior gustatory IC displayed fewer aversive reactions to sucrose following this initial LiCl injection. We further assessed whether the failure to integrate interoceptive feedback with ongoing taste-guided behavior impaired acquisition and/or expression of conditioned aversion and/or avoidance in these same rats. Although, as a group, LiCl-injected rats with IC lesions subsequently avoided the sugar in a 48-h two-bottle test, their preference for sucrose was significantly greater than that of the LiCl-injected neurally-intact rats. Overall lesion size, as well as proportion of the posterior gustatory and/or anterior visceral IC were each associated with impaired avoidance. These findings reveal new roles for the posterior gustatory and anterior visceral ICs in multisensory integrative function.

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          Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing

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            The insular cortex

            Whether you see the person you are in love with, try to listen to your own heartbeat, suffer from a headache, or crave for a chocolate cookie, one part of your brain is sure to increase its activity strongly: the insular cortex. The insular cortex, or 'insula' for short, is part of the cerebral cortex. J.C. Reil, a German neurologist, first named this brain structure in the early 19th century. Subsequent research findings have implicated the insula in an overwhelming variety of functions ranging from sensory processing to representing feelings and emotions, autonomical and motor control, risk prediction and decision-making, bodily- and self-awareness, and complex social functions like empathy. How is one single brain area involved in so many different tasks? Is the insula comprised of several functional regions? How are these related? And, are there any common themes underlying the apparently so heterogeneous roles of the insula?
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              A whole-brain connectivity map of mouse insular cortex

              The insular cortex (IC) plays key roles in emotional and regulatory brain functions and is affected across psychiatric diseases. However, the brain-wide connections of the mouse IC have not been comprehensively mapped. Here, we traced the whole-brain inputs and outputs of the mouse IC across its rostro-caudal extent. We employed cell-type-specific monosynaptic rabies virus tracings to characterize afferent connections onto either excitatory or inhibitory IC neurons, and adeno-associated viral tracings to label excitatory efferent axons. While the connectivity between the IC and other cortical regions was highly bidirectional, the IC connectivity with subcortical structures was often unidirectional, revealing prominent cortical-to-subcortical or subcortical-to-cortical pathways. The posterior and medial IC exhibited resembling connectivity patterns, while the anterior IC connectivity was distinct, suggesting two major functional compartments. Our results provide insights into the anatomical architecture of the mouse IC and thus a structural basis to guide investigations into its complex functions.
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                Author and article information

                Journal
                eNeuro
                eNeuro
                eneuro
                eNeuro
                eNeuro
                Society for Neuroscience
                2373-2822
                31 May 2022
                6 July 2022
                Jul-Aug 2022
                : 9
                : 4
                : ENEURO.0527-21.2022
                Affiliations
                [1 ]Neuroscience Graduate Program, University of Southern California , Los Angeles, CA 90089
                [2 ]Department of Psychology, Stetson University , DeLand, FL 32723
                [3 ]Department of Psychology and Program in Neuroscience, Florida State University , Tallahassee, FL 32306
                [4 ]Department of Biology, Stetson University , DeLand, FL 32723
                [5 ]Department of Biological Sciences, University of Southern California , Los Angeles, CA 90089
                [6 ]Department of Morphological and Physiological Sciences, Kumamoto University , Kumamoto, Japan 860-8555
                Author notes

                Author contributions: C.T.K., A.C.S., and L.A.S. designed research; A-H.J., C.T.K., G.D.B., M.K., C.G., K.H., and L.A.S. performed research; A-H.J., C.K., and L.A.S. analyzed data; A-H.J. and L.A.S. wrote the paper.

                This work was supported by the National Institute of Deafness and Communications Disorders Grant R01 DC009821 (to A.C.S.), Dornsife institutional start-up funds (L.A.S.), and a Dornsife Neuroscience program graduate research fellowship (A-H.J.).

                The authors declare no competing financial interests.

                Correspondence should be addressed to Lindsey A. Schier at lschier@ 123456usc.edu .
                Article
                eN-NWR-0527-21
                10.1523/ENEURO.0527-21.2022
                9267001
                35641228
                93716249-79bb-4d3b-b930-c6aeee736f6b
                Copyright © 2022 Jung et al.

                This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license, which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.

                History
                : 21 December 2021
                : 16 May 2022
                : 19 May 2022
                Page count
                Figures: 7, Tables: 9, Equations: 0, References: 42, Pages: 15, Words: 00
                Funding
                Funded by: HHS | NIH | National Institute on Deafness and Other Communication Disorders (NIDCD), doi 10.13039/100000055;
                Award ID: DC009821
                Funded by: University of Southern California (USC), doi 10.13039/100006034;
                Categories
                5
                Research Article: New Research
                Integrative Systems
                Custom metadata
                July/August 2022

                brain mapping,food reward,gustatory cortex,interoception,taste hedonics,visceral cortex

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