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      Learning and memory disabilities in IUGR babies: Functional and molecular analysis in a rat model

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          Abstract

          1. Introduction

          Intrauterine growth restriction ( IUGR) is the failure of the fetus to achieve its inherent growth potential, and it has frequently been associated with neurodevelopmental problems in childhood. Neurological disorders are mostly associated with IUGR babies with an abnormally high cephalization index ( CI) and a brain sparing effect. However, a similar correlation has never been demonstrated in an animal model. The aim of this study was to determine the correlations between CI, functional deficits in learning and memory and alterations in synaptic proteins in a rat model of IUGR.

          2. Methods

          Utero‐placental insufficiency was induced by meso‐ovarian vessel cauterization ( CMO) in pregnant rats at embryonic day 17 (E17). Learning performance in an aquatic learning test was evaluated 25 days after birth and during 10 days. Some synaptic proteins were analyzed ( PSD95, Synaptophysin) by Western blot and immunohistochemistry.

          3. Results

          Placental insufficiency in CMO pups was associated with spatial memory deficits, which are correlated with a CI above the normal range. CMO pups presented altered levels of synaptic proteins PSD95 and synaptophysin in the hippocampus.

          4. Conclusions

          The results of this study suggest that learning disabilities may be associated with altered development of excitatory neurotransmission and synaptic plasticity. Although interspecific differences in fetal response to placental insufficiency should be taken into account, the translation of these data to humans suggest that both IUGR babies and babies with a normal birth weight but with intrauterine Doppler alterations and abnormal CI should be closely followed to detect neurodevelopmental alterations during the postnatal period.

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          Most cited references53

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          PSD-95 is required for activity-driven synapse stabilization.

          The activity-dependent regulation of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA)-type glutamate receptors and the stabilization of synapses are critical to synaptic development and plasticity. One candidate molecule implicated in maturation, synaptic strengthening, and plasticity is PSD-95. Here we find that acute knockdown of PSD-95 in brain slice cultures by RNAi arrests the normal development of synaptic structure and function that is driven by spontaneous activity. Surprisingly, PSD-95 is not necessary for the induction and early expression of long-term potentiation (LTP). However, knockdown of PSD-95 leads to smaller increases in spine size after chemically induced LTP. Furthermore, although at this age spine turnover is normally low and LTP produces a transient increase, in cells with reduced PSD-95 spine turnover is high and remains increased after LTP. Taken together, our data support a model in which appropriate levels of PSD-95 are required for activity-dependent synapse stabilization after initial phases of synaptic potentiation.
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            Intrauterine growth retardation leads to the development of type 2 diabetes in the rat.

            Intrauterine growth retardation has been linked to the development of type 2 diabetes in later life. The mechanisms underlying this phenomenon are unknown. We have developed a model of uteroplacental insufficiency, a common cause of intrauterine growth retardation, in the rat. Bilateral uterine artery ligation was performed on day 19 of gestation (term is 22 days) in the pregnant rat; sham-operated pregnant rats served as controls. Birth weights of intrauterine growth-retarded (IUGR) animals were significantly lower than those of controls until approximately 7 weeks of age, when IUGR rats caught up to controls. Between 7 and 10 weeks of age, the growth of IUGR rats accelerated and surpassed that of controls, and by 26 weeks of age, IUGR rats were obese (P < 0.05 vs. controls). No significant differences were observed in blood glucose and plasma insulin levels at 1 week of age. However, between 7 and 10 weeks of age, IUGR rats developed mild fasting hyperglycemia and hyperinsulinemia (P < 0.05 vs. controls). At age 26 weeks, IUGR animals had markedly elevated levels of glucose (P < 0.05 vs. controls). IUGR animals were glucose-intolerant and insulin-resistant at an early age. First-phase insulin secretion in response to glucose was also impaired early in life in IUGR rats, before the onset of hyperglycemia. There were no significant differences in beta-cell mass, islet size, or pancreatic weight between IUGR and control animals at 1 and 7 weeks of age. However, in 15-week-old IUGR rats, the relative beta-cell mass was 50% that of controls, and by 26 weeks of age, beta-cell mass was less than one-third that of controls (P < 0.05). The data presented here support the hypothesis that an abnormal intrauterine milieu can induce permanent changes in glucose homeostasis after birth and lead to type 2 diabetes in adulthood.
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              Multiple autism-linked genes mediate synapse elimination via proteasomal degradation of a synaptic scaffold PSD-95.

              The activity-dependent transcription factor myocyte enhancer factor 2 (MEF2) induces excitatory synapse elimination in mouse neurons, which requires fragile X mental retardation protein (FMRP), an RNA-binding protein implicated in human cognitive dysfunction and autism. We report here that protocadherin 10 (Pcdh10), an autism-spectrum disorders gene, is necessary for this process. MEF2 and FMRP cooperatively regulate the expression of Pcdh10. Upon MEF2 activation, PSD-95 is ubiquitinated by the ubiquitin E3 ligase murine double minute 2 (Mdm2) and then binds to Pcdh10, which links it to the proteasome for degradation. Blockade of the Pcdh10-proteasome interaction inhibits MEF2-induced PSD-95 degradation and synapse elimination. In FMRP-lacking neurons, elevated protein levels of eukaryotic translation elongation factor 1 α (EF1α), an Mdm2-interacting protein and FMRP target mRNA, sequester Mdm2 and prevent MEF2-induced PSD-95 ubiquitination and synapse elimination. Together, our findings reveal roles for multiple autism-linked genes in activity-dependent synapse elimination. Copyright © 2012 Elsevier Inc. All rights reserved.
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                Author and article information

                Contributors
                mcamprubic@hsjdbcn.org
                salcantara@ub.edu
                Journal
                Brain Behav
                Brain Behav
                10.1002/(ISSN)2157-9032
                BRB3
                Brain and Behavior
                John Wiley and Sons Inc. (Hoboken )
                2162-3279
                07 February 2017
                March 2017
                : 7
                : 3 ( doiID: 10.1002/brb3.2017.7.issue-3 )
                : e00631
                Affiliations
                [ 1 ] Neonatology Service Sant Joan de Déu BCNatal Hospital Sant Joan de Déu i ClínicUniversity of Barcelona BarcelonaSpain
                [ 2 ] Department of Pathology and Experimental Therapeutics School of MedicineUniversity of Barcelona BarcelonaSpain
                [ 3 ] Department of Molecular Biology and Biochemical EngineeringUniversity Pablo de Olavide – CABIMER – CIBERDEM SevillaSpain
                [ 4 ] Pediatrics ServiceHospital Álvaro Cunqueiro VigoSpain
                [ 5 ]Universitat Internacional de Catalunya Sant Cugat del Vallès BarcelonaSpain
                [ 6 ]Present address: Department of Neurology Feinberg School of MedicineNorthwestern University Chicago IL 60611USA
                Author notes
                [*] [* ] Correspondence

                Soledad Alcántara, Department of Pathology and Experimental Therapeutics, School of Medicine and Health Sciences, University of Barcelona, Barcelona, Spain.

                Email: salcantara@ 123456ub.edu

                Marta Camprubí Camprubí, Neonatology Service, Sant Joan de Déu, BCNatal, Hospital Sant Joan de Déu i Clínic, University of Barcelona, Barcelona, Spain.

                Email: mcamprubic@ 123456hsjdbcn.org

                Author information
                http://orcid.org/0000-0001-9202-4664
                Article
                BRB3631
                10.1002/brb3.631
                5346519
                28293472
                fea20d27-d84f-4f8e-9d3b-bd713da68b35
                © 2017 The Authors. Brain and Behavior published by Wiley Periodicals, Inc.

                This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 19 March 2016
                : 22 July 2016
                : 30 November 2016
                Page count
                Figures: 4, Tables: 2, Pages: 14, Words: 8662
                Funding
                Funded by: Spanish Ministerio de Economía y Competitividad
                Award ID: MAT2011‐29778‐C02‐02
                Funded by: European Regional Development Fund
                Award ID: BFU2014‐55373‐R
                Funded by: Generalitat de Catalunya
                Award ID: 2014 SGR 1178
                Categories
                Original Research
                Original Research
                Custom metadata
                2.0
                brb3631
                March 2017
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.0.8 mode:remove_FC converted:12.03.2017

                Neurosciences
                cephalization index,intrauterine growth restriction,learning,placental insufficiency,spatial memory,synaptic plasticity

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