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A Neonatal Piglet Model for Investigating Brain and Cognitive Development in Small for Gestational Age Human Infants
The piglet was investigated as a potential model for studying brain and cognitive deficits associated with being born small for gestational age (SGA). Naturally farrowed SGA (0.7–1.0 kg BW) and average for gestational age (AGA, 1.3–1.6 kg BW) piglets were obtained on postnatal day (PD) 2, placed in...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3956804/ https://www.ncbi.nlm.nih.gov/pubmed/24637829 http://dx.doi.org/10.1371/journal.pone.0091951 |
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author | Radlowski, Emily C. Conrad, Matthew S. Lezmi, Stephane Dilger, Ryan N. Sutton, Brad Larsen, Ryan Johnson, Rodney W. |
author_facet | Radlowski, Emily C. Conrad, Matthew S. Lezmi, Stephane Dilger, Ryan N. Sutton, Brad Larsen, Ryan Johnson, Rodney W. |
author_sort | Radlowski, Emily C. |
collection | PubMed |
description | The piglet was investigated as a potential model for studying brain and cognitive deficits associated with being born small for gestational age (SGA). Naturally farrowed SGA (0.7–1.0 kg BW) and average for gestational age (AGA, 1.3–1.6 kg BW) piglets were obtained on postnatal day (PD) 2, placed in individual cages, and provided a nutritionally adequate milk replacer diet (285 ml/kg/d). Beginning at PD14, performance in a spatial T-maze task was assessed. At PD28, piglets were anesthetized for magnetic resonance (MR) imaging to assess brain structure (voxel-based morphometry), connectivity (diffusion-tensor imaging) and metabolites in the hippocampus and corpus callosum (proton MR spectroscopy). Piglets born SGA showed compensatory growth such that BW of SGA and AGA piglets was similar (P>0.05), by PD15. Birth weight affected maze performance, with SGA piglets taking longer to reach criterion than AGA piglets (p<0.01). Total brain volume of SGA and AGA piglets was similar (P<0.05), but overall, SGA piglets had less gray matter than AGA piglets (p<0.01) and tended to have a smaller internal capsule (p = 0.07). Group comparisons between SGA and AGA piglets defined 9 areas (≥ 20 clusters) where SGA piglets had less white matter (p<0.01); 2 areas where SGA piglets had more white matter (p<0.01); and 3 areas where SGA piglets had more gray matter (p<0.01). The impact of being born SGA on white matter was supported by a lower (p<0.04) fractional anisotropy value for SGA piglets, suggesting reduced white matter development and connectivity. None of the metabolites measured were different between groups. Collectively, the results show that SGA piglets have spatial learning deficits and abnormal development of white matter. As learning deficits and abnormalities in white matter are common in SGA human infants, the piglet is a tractable translational model that can be used to investigate SGA-associated cognitive deficits and potential interventions. |
format | Online Article Text |
id | pubmed-3956804 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-39568042014-03-18 A Neonatal Piglet Model for Investigating Brain and Cognitive Development in Small for Gestational Age Human Infants Radlowski, Emily C. Conrad, Matthew S. Lezmi, Stephane Dilger, Ryan N. Sutton, Brad Larsen, Ryan Johnson, Rodney W. PLoS One Research Article The piglet was investigated as a potential model for studying brain and cognitive deficits associated with being born small for gestational age (SGA). Naturally farrowed SGA (0.7–1.0 kg BW) and average for gestational age (AGA, 1.3–1.6 kg BW) piglets were obtained on postnatal day (PD) 2, placed in individual cages, and provided a nutritionally adequate milk replacer diet (285 ml/kg/d). Beginning at PD14, performance in a spatial T-maze task was assessed. At PD28, piglets were anesthetized for magnetic resonance (MR) imaging to assess brain structure (voxel-based morphometry), connectivity (diffusion-tensor imaging) and metabolites in the hippocampus and corpus callosum (proton MR spectroscopy). Piglets born SGA showed compensatory growth such that BW of SGA and AGA piglets was similar (P>0.05), by PD15. Birth weight affected maze performance, with SGA piglets taking longer to reach criterion than AGA piglets (p<0.01). Total brain volume of SGA and AGA piglets was similar (P<0.05), but overall, SGA piglets had less gray matter than AGA piglets (p<0.01) and tended to have a smaller internal capsule (p = 0.07). Group comparisons between SGA and AGA piglets defined 9 areas (≥ 20 clusters) where SGA piglets had less white matter (p<0.01); 2 areas where SGA piglets had more white matter (p<0.01); and 3 areas where SGA piglets had more gray matter (p<0.01). The impact of being born SGA on white matter was supported by a lower (p<0.04) fractional anisotropy value for SGA piglets, suggesting reduced white matter development and connectivity. None of the metabolites measured were different between groups. Collectively, the results show that SGA piglets have spatial learning deficits and abnormal development of white matter. As learning deficits and abnormalities in white matter are common in SGA human infants, the piglet is a tractable translational model that can be used to investigate SGA-associated cognitive deficits and potential interventions. Public Library of Science 2014-03-17 /pmc/articles/PMC3956804/ /pubmed/24637829 http://dx.doi.org/10.1371/journal.pone.0091951 Text en © 2014 Radlowski et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Radlowski, Emily C. Conrad, Matthew S. Lezmi, Stephane Dilger, Ryan N. Sutton, Brad Larsen, Ryan Johnson, Rodney W. A Neonatal Piglet Model for Investigating Brain and Cognitive Development in Small for Gestational Age Human Infants |
title | A Neonatal Piglet Model for Investigating Brain and Cognitive Development in Small for Gestational Age Human Infants |
title_full | A Neonatal Piglet Model for Investigating Brain and Cognitive Development in Small for Gestational Age Human Infants |
title_fullStr | A Neonatal Piglet Model for Investigating Brain and Cognitive Development in Small for Gestational Age Human Infants |
title_full_unstemmed | A Neonatal Piglet Model for Investigating Brain and Cognitive Development in Small for Gestational Age Human Infants |
title_short | A Neonatal Piglet Model for Investigating Brain and Cognitive Development in Small for Gestational Age Human Infants |
title_sort | neonatal piglet model for investigating brain and cognitive development in small for gestational age human infants |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3956804/ https://www.ncbi.nlm.nih.gov/pubmed/24637829 http://dx.doi.org/10.1371/journal.pone.0091951 |
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