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      Brain Lateralization in Mice Is Associated with Zinc Signaling and Altered in Prenatal Zinc Deficient Mice That Display Features of Autism Spectrum Disorder

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          Abstract

          A number of studies have reported changes in the hemispheric dominance in autism spectrum disorder (ASD) patients on functional, biochemical, and morphological level. Since asymmetry of the brain is also found in many vertebrates, we analyzed whether prenatal zinc deficient (PZD) mice, a mouse model with ASD like behavior, show alterations regarding brain lateralization on molecular and behavioral level. Our results show that hemisphere-specific expression of marker genes is abolished in PZD mice on mRNA and protein level. Using magnetic resonance imaging, we found an increased striatal volume in PZD mice with no change in total brain volume. Moreover, behavioral patterns associated with striatal lateralization are altered and the lateralized expression of dopamine receptor 1 (DR1) in the striatum of PZD mice was changed. We conclude that zinc signaling during brain development has a critical role in the establishment of brain lateralization in mice.

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          Shank3 mutant mice display autistic-like behaviours and striatal dysfunction

          Autism spectrum disorders (ASDs) comprise a range of disorders that share a core of neurobehavioural deficits characterized by widespread abnormalities in social interactions, deficits in communication as well as restricted interests and repetitive behaviours. The neurological basis and circuitry mechanisms underlying these abnormal behaviours are poorly understood. Shank3 is a postsynaptic protein, whose disruption at the genetic level is thought to be responsible for development of 22q13 deletion syndrome (Phelan-McDermid Syndrome) and other non-syndromic ASDs. Here we show that mice with Shank3 gene deletions exhibit self-injurious repetitive grooming and deficits in social interaction. Cellular, electrophysiological and biochemical analyses uncovered defects at striatal synapses and cortico-striatal circuits in Shank3 mutant mice. Our findings demonstrate a critical role for Shank3 in the normal development of neuronal connectivity and establish causality between a disruption in the Shank3 gene and the genesis of autistic like-behaviours in mice.
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            Mapping brain asymmetry.

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              Survival with an asymmetrical brain: advantages and disadvantages of cerebral lateralization.

              Recent evidence in natural and semi-natural settings has revealed a variety of left-right perceptual asymmetries among vertebrates. These include preferential use of the left or right visual hemifield during activities such as searching for food, agonistic responses, or escape from predators in animals as different as fish, amphibians, reptiles, birds, and mammals. There are obvious disadvantages in showing such directional asymmetries because relevant stimuli may be located to the animal's left or right at random; there is no a priori association between the meaning of a stimulus (e.g., its being a predator or a food item) and its being located to the animal's left or right. Moreover, other organisms (e.g., predators) could exploit the predictability of behavior that arises from population-level lateral biases. It might be argued that lateralization of function enhances cognitive capacity and efficiency of the brain, thus counteracting the ecological disadvantages of lateral biases in behavior. However, such an increase in brain efficiency could be obtained by each individual being lateralized without any need to align the direction of the asymmetry in the majority of the individuals of the population. Here we argue that the alignment of the direction of behavioral asymmetries at the population level arises as an "evolutionarily stable strategy" under "social" pressures occurring when individually asymmetrical organisms must coordinate their behavior with the behavior of other asymmetrical organisms of the same or different species.
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                Author and article information

                Contributors
                Journal
                Front Mol Neurosci
                Front Mol Neurosci
                Front. Mol. Neurosci.
                Frontiers in Molecular Neuroscience
                Frontiers Media S.A.
                1662-5099
                15 January 2018
                2017
                : 10
                : 450
                Affiliations
                [1] 1Institute for Anatomy and Cell Biology, Ulm University , Ulm, Germany
                [2] 2Cellular Neurobiology and Neuro-Nanotechnology Laboratory, Department of Biological Sciences, University of Limerick , Limerick, Ireland
                [3] 3WG Molecular Analysis of Synaptopathies, Neurology Department, Neurocenter of Ulm University , Ulm, Germany
                [4] 4Core Facility Small Animal Imaging, Ulm University , Ulm, Germany
                [5] 5Department of Internal Medicine II, Ulm University Medical Center , Ulm, Germany
                [6] 6Bernal Institute, University of Limerick , Limerick, Ireland
                [7] 7Health Research Institute (HRI), University of Limerick , Limerick, Ireland
                Author notes

                Edited by: Eunjoon Kim, Institute for Basic Science (IBS), South Korea

                Reviewed by: Markus Wöhr, Philipps University of Marburg, Germany; Chiara Verpelli, Istituto di Neuroscienze (CNR), Italy

                These authors have contributed equally to this work.

                Article
                10.3389/fnmol.2017.00450
                5775238
                29379414
                18e0d9ba-b29c-4ff5-9b63-2f3ef2282ca9
                Copyright © 2018 Grabrucker, Haderspeck, Sauer, Kittelberger, Asoglu, Abaei, Rasche, Schön, Boeckers and Grabrucker.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 17 October 2017
                : 22 December 2017
                Page count
                Figures: 5, Tables: 0, Equations: 0, References: 76, Pages: 13, Words: 0
                Categories
                Neuroscience
                Original Research

                Neurosciences
                zn,hemisphere dominance,asd,synapse,trace metal,connectivity
                Neurosciences
                zn, hemisphere dominance, asd, synapse, trace metal, connectivity

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