Cortical Processing of Multimodal Sensory Learning in Human Neonates

Author:

Dall'Orso S123,Fifer W P4,Balsam P D4,Brandon J2,O’Keefe C2,Poppe T2,Vecchiato K2,Edwards A D12,Burdet E1,Arichi T125ORCID

Affiliation:

1. Department of Bioengineering, Imperial College London, London SW7 2AZ, UK

2. Centre for the Developing Brain, School of Biomedical Engineering and Imaging Sciences, Kings College London, London SE1 7EH, UK

3. Department of Electrical Engineering, Chalmers University of Technology, Gothenburg 412 96, Sweden

4. Department of Psychiatry, Columbia University, New York 10032, NY

5. Paediatric Neurosciences, Evelina London Children’s Hospital, St Thomas’ Hospital, London SE1 7EH, UK

Abstract

Abstract Following birth, infants must immediately process and rapidly adapt to the array of unknown sensory experiences associated with their new ex-utero environment. However, although it is known that unimodal stimuli induce activity in the corresponding primary sensory cortices of the newborn brain, it is unclear how multimodal stimuli are processed and integrated across modalities. The latter is essential for learning and understanding environmental contingencies through encoding relationships between sensory experiences; and ultimately likely subserves development of life-long skills such as speech and language. Here, for the first time, we map the intracerebral processing which underlies auditory-sensorimotor classical conditioning in a group of 13 neonates (median gestational age at birth: 38 weeks + 4 days, range: 32 weeks + 2 days to 41 weeks + 6 days; median postmenstrual age at scan: 40 weeks + 5 days, range: 38 weeks + 3 days to 42 weeks + 1 days) with blood-oxygen-level-dependent (BOLD) functional magnetic resonance imaging (MRI) and magnetic resonance (MR) compatible robotics. We demonstrate that classical conditioning can induce crossmodal changes within putative unimodal sensory cortex even in the absence of its archetypal substrate. Our results also suggest that multimodal learning is associated with network wide activity within the conditioned neural system. These findings suggest that in early life, external multimodal sensory stimulation and integration shapes activity in the developing cortex and may influence its associated functional network architecture.

Funder

Engineering and Physical Sciences Research Council

Chalmers University of Technology Area of Advance in Life Science Engineering

Medical Research Council

European Commission

UK Engineering and Physical Sciences Research Council

National Institute for Health Research

Wellcome Engineering and Physical Sciences Research Council

Centre for Medical Engineering at Kings College London

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Cognitive Neuroscience

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3