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      Enhanced Neonatal Brain Responses To Sung Streams Predict Vocabulary Outcomes By Age 18 Months

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          Abstract

          Words and melodies are some of the basic elements infants are able to extract early in life from the auditory input. Whether melodic cues contained in songs can facilitate word-form extraction immediately after birth remained unexplored. Here, we provided converging neural and computational evidence of the early benefit of melodies for language acquisition. Twenty-eight neonates were tested on their ability to extract word-forms from continuous flows of sung and spoken syllabic sequences. We found different brain dynamics for sung and spoken streams and observed successful detection of word-form violations in the sung condition only. Furthermore, neonatal brain responses for sung streams predicted expressive vocabulary at 18 months as demonstrated by multiple regression and cross-validation analyses. These findings suggest that early neural individual differences in prosodic speech processing might be a good indicator of later language outcomes and could be considered as a relevant factor in the development of infants’ language skills.

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          Most cited references63

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          Specification of cerebral cortical areas.

          P Rakic (1988)
          How the immense population of neurons that constitute the human cerebral neocortex is generated from progenitors lining the cerebral ventricle and then distributed to appropriate layers of distinctive cytoarchitectonic areas can be explained by the radial unit hypothesis. According to this hypothesis, the ependymal layer of the embryonic cerebral ventricle consists of proliferative units that provide a proto-map of prospective cytoarchitectonic areas. The output of the proliferative units is translated via glial guides to the expanding cortex in the form of ontogenetic columns, whose final number for each area can be modified through interaction with afferent input. Data obtained through various advanced neurobiological techniques, including electron microscopy, immunocytochemistry, [3H]thymidine and receptor autoradiography, retrovirus gene transfer, neural transplants, and surgical or genetic manipulation of cortical development, furnish new details about the kinetics of cell proliferation, their lineage relationships, and phenotypic expression that favor this hypothesis. The radial unit model provides a framework for understanding cerebral evolution, epigenetic regulation of the parcellation of cytoarchitectonic areas, and insight into the pathogenesis of certain cortical disorders in humans.
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            Reward-motivated learning: mesolimbic activation precedes memory formation.

            We examined anticipatory mechanisms of reward-motivated memory formation using event-related FMRI. In a monetary incentive encoding task, cues signaled high- or low-value reward for memorizing an upcoming scene. When tested 24 hr postscan, subjects were significantly more likely to remember scenes that followed cues for high-value rather than low-value reward. A monetary incentive delay task independently localized regions responsive to reward anticipation. In the encoding task, high-reward cues preceding remembered but not forgotten scenes activated the ventral tegmental area, nucleus accumbens, and hippocampus. Across subjects, greater activation in these regions predicted superior memory performance. Within subject, increased correlation between the hippocampus and ventral tegmental area was associated with enhanced long-term memory for the subsequent scene. These findings demonstrate that brain activation preceding stimulus encoding can predict declarative memory formation. The findings are consistent with the hypothesis that reward motivation promotes memory formation via dopamine release in the hippocampus prior to learning.
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              A small step for the cell, a giant leap for mankind: a hypothesis of neocortical expansion during evolution.

              The more than 1000-fold increase in the cortical surface without a comparable increase in its thickness during mammalian evolution is explained in the context of the radial-unit hypothesis of cortical development. According to the proposed model, cortical expansion is the result of changes in proliferation kinetics that increase the number of radial columnar units without changing the number of neurons within each unit significantly. Thus, mutation of a regulatory gene(s) that controls the timing and ratio of symmetric and asymmetric modes of cell divisions in the proliferative zone, coupled with radial constraints in the distribution of migrating neurons, could create an expanded cortical plate with enhanced capacity for establishing new patterns of connectivity that are validated through natural selection.
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                Author and article information

                Contributors
                fclement24@hotmail.com
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                29 September 2017
                29 September 2017
                2017
                : 7
                : 12451
                Affiliations
                [1 ]ISNI 0000 0004 0427 2257, GRID grid.418284.3, Cognition and Brain Plasticity Group, Bellvitge Biomedical Research Institute IDIBELL, L’Hospitalet de Llobregat, ; Barcelona, Spain
                [2 ]ISNI 0000 0004 1937 0247, GRID grid.5841.8, Department of Cognition, Development and Educational Psychology, University of Barcelona, ; Barcelona, Spain
                [3 ]ISNI 0000 0001 0663 8628, GRID grid.411160.3, Institut de Recerca Pediàtrica Hospital Sant Joan de Déu, ; Barcelona, Spain
                [4 ]ISNI 0000 0004 4650 2882, GRID grid.462486.a, Aix Marseille Univ, CNRS, INT, Inst Neurosci Timone, ; Marseille, France
                [5 ]ISNI 0000 0001 0663 8628, GRID grid.411160.3, Department of Neonatalogy, Hospital Sant Joan de Déu, ; Barcelona, Spain
                [6 ]ISNI 0000 0004 1937 0247, GRID grid.5841.8, Institut de Neurociències, University of Barcelona, ; Barcelona, Spain
                [7 ]ISNI 0000 0000 9601 989X, GRID grid.425902.8, Institució Catalana de Recerca i Estudis Avançats, ICREA, ; Barcelona, Spain
                Author information
                http://orcid.org/0000-0003-2271-6942
                http://orcid.org/0000-0001-8410-0962
                Article
                12798
                10.1038/s41598-017-12798-2
                5622081
                28963569
                99c57bb3-e3fd-4786-a0a7-aaff838a9084
                © The Author(s) 2017

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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                : 15 June 2017
                : 15 September 2017
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