Limited effects of preterm birth and the first enteral nutrition on cerebellum morphology and gene expression in piglets

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Standard

Limited effects of preterm birth and the first enteral nutrition on cerebellum morphology and gene expression in piglets. / Bergström, Anders; Kaalund, Sanne Simone; Skovgaard, Kerstin; Andersen, Anders Daniel; Pakkenberg, Bente; Rosenørn, Ann; van Elburg, Ruurd M.; Thymann, Thomas; Greisen, Gorm; Sangild, Per Torp.

I: Physiological Reports, Bind 4, Nr. 14, e12871, 26.07.2016.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Bergström, A, Kaalund, SS, Skovgaard, K, Andersen, AD, Pakkenberg, B, Rosenørn, A, van Elburg, RM, Thymann, T, Greisen, G & Sangild, PT 2016, 'Limited effects of preterm birth and the first enteral nutrition on cerebellum morphology and gene expression in piglets', Physiological Reports, bind 4, nr. 14, e12871. https://doi.org/10.14814/phy2.12871

APA

Bergström, A., Kaalund, S. S., Skovgaard, K., Andersen, A. D., Pakkenberg, B., Rosenørn, A., van Elburg, R. M., Thymann, T., Greisen, G., & Sangild, P. T. (2016). Limited effects of preterm birth and the first enteral nutrition on cerebellum morphology and gene expression in piglets. Physiological Reports, 4(14), [e12871]. https://doi.org/10.14814/phy2.12871

Vancouver

Bergström A, Kaalund SS, Skovgaard K, Andersen AD, Pakkenberg B, Rosenørn A o.a. Limited effects of preterm birth and the first enteral nutrition on cerebellum morphology and gene expression in piglets. Physiological Reports. 2016 jul. 26;4(14). e12871. https://doi.org/10.14814/phy2.12871

Author

Bergström, Anders ; Kaalund, Sanne Simone ; Skovgaard, Kerstin ; Andersen, Anders Daniel ; Pakkenberg, Bente ; Rosenørn, Ann ; van Elburg, Ruurd M. ; Thymann, Thomas ; Greisen, Gorm ; Sangild, Per Torp. / Limited effects of preterm birth and the first enteral nutrition on cerebellum morphology and gene expression in piglets. I: Physiological Reports. 2016 ; Bind 4, Nr. 14.

Bibtex

@article{e328605371e54b54bb9fc992dc0ea527,
title = "Limited effects of preterm birth and the first enteral nutrition on cerebellum morphology and gene expression in piglets",
abstract = "Preterm pigs show many signs of immaturity that are characteristic of preterm infants. In preterm infants, the cerebellum grows particularly rapid and hypoplasia and cellular lesions are associated with motor dysfunction and cognitive deficits. We hypothesized that functional brain delays observed in preterm pigs would be paralleled by both structural and molecular differences in the cerebellum relative to term born piglets. Cerebella were collected from term (n = 56) and preterm (90% gestation, n = 112) pigs at 0, 5, and 26 days after birth for stereological volume estimations, large-scale qPCR gene expression analyses (selected neurodevelopmental genes) and western blot protein expression analysis (Sonic Hedgehog pathway). Memory and learning was tested using a T-maze, documenting that preterm pigs showed delayed learning. Preterm pigs also showed reduced volume of both white and gray matter at all three ages but the proportion of white matter increased postnatally, relative to term pigs. Early initiation of enteral nutrition had limited structural or molecular effects. The Sonic Hedgehog pathway was unaffected by preterm birth. Few differences in expression of the selected genes were found, except consistently higher mRNA levels of Midkine, p75, and Neurotrophic factor 3 in the preterm cerebellum postnatally, probably reflecting an adaptive response to preterm birth. Pig cerebellar development appears more affected by postconceptional age than by environmental factors at birth or postnatally. Compensatory mechanisms following preterm birth may include faster white matter growth and increased expression of selected genes for neurotrophic factors and regulation of angiogenesis. While the pig cerebellum is immature in 90% gestation preterm pigs, it appears relatively mature and resilient toward environmental factors.",
keywords = "Journal Article",
author = "Anders Bergstr{\"o}m and Kaalund, {Sanne Simone} and Kerstin Skovgaard and Andersen, {Anders Daniel} and Bente Pakkenberg and Ann Rosen{\o}rn and {van Elburg}, {Ruurd M.} and Thomas Thymann and Gorm Greisen and Sangild, {Per Torp}",
note = "{\textcopyright} 2016 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of the American Physiological Society and The Physiological Society.",
year = "2016",
month = jul,
day = "26",
doi = "10.14814/phy2.12871",
language = "English",
volume = "4",
journal = "Physiological Reports",
issn = "2051-817X",
publisher = "Wiley Periodicals, Inc.",
number = "14",

}

RIS

TY - JOUR

T1 - Limited effects of preterm birth and the first enteral nutrition on cerebellum morphology and gene expression in piglets

AU - Bergström, Anders

AU - Kaalund, Sanne Simone

AU - Skovgaard, Kerstin

AU - Andersen, Anders Daniel

AU - Pakkenberg, Bente

AU - Rosenørn, Ann

AU - van Elburg, Ruurd M.

AU - Thymann, Thomas

AU - Greisen, Gorm

AU - Sangild, Per Torp

N1 - © 2016 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of the American Physiological Society and The Physiological Society.

PY - 2016/7/26

Y1 - 2016/7/26

N2 - Preterm pigs show many signs of immaturity that are characteristic of preterm infants. In preterm infants, the cerebellum grows particularly rapid and hypoplasia and cellular lesions are associated with motor dysfunction and cognitive deficits. We hypothesized that functional brain delays observed in preterm pigs would be paralleled by both structural and molecular differences in the cerebellum relative to term born piglets. Cerebella were collected from term (n = 56) and preterm (90% gestation, n = 112) pigs at 0, 5, and 26 days after birth for stereological volume estimations, large-scale qPCR gene expression analyses (selected neurodevelopmental genes) and western blot protein expression analysis (Sonic Hedgehog pathway). Memory and learning was tested using a T-maze, documenting that preterm pigs showed delayed learning. Preterm pigs also showed reduced volume of both white and gray matter at all three ages but the proportion of white matter increased postnatally, relative to term pigs. Early initiation of enteral nutrition had limited structural or molecular effects. The Sonic Hedgehog pathway was unaffected by preterm birth. Few differences in expression of the selected genes were found, except consistently higher mRNA levels of Midkine, p75, and Neurotrophic factor 3 in the preterm cerebellum postnatally, probably reflecting an adaptive response to preterm birth. Pig cerebellar development appears more affected by postconceptional age than by environmental factors at birth or postnatally. Compensatory mechanisms following preterm birth may include faster white matter growth and increased expression of selected genes for neurotrophic factors and regulation of angiogenesis. While the pig cerebellum is immature in 90% gestation preterm pigs, it appears relatively mature and resilient toward environmental factors.

AB - Preterm pigs show many signs of immaturity that are characteristic of preterm infants. In preterm infants, the cerebellum grows particularly rapid and hypoplasia and cellular lesions are associated with motor dysfunction and cognitive deficits. We hypothesized that functional brain delays observed in preterm pigs would be paralleled by both structural and molecular differences in the cerebellum relative to term born piglets. Cerebella were collected from term (n = 56) and preterm (90% gestation, n = 112) pigs at 0, 5, and 26 days after birth for stereological volume estimations, large-scale qPCR gene expression analyses (selected neurodevelopmental genes) and western blot protein expression analysis (Sonic Hedgehog pathway). Memory and learning was tested using a T-maze, documenting that preterm pigs showed delayed learning. Preterm pigs also showed reduced volume of both white and gray matter at all three ages but the proportion of white matter increased postnatally, relative to term pigs. Early initiation of enteral nutrition had limited structural or molecular effects. The Sonic Hedgehog pathway was unaffected by preterm birth. Few differences in expression of the selected genes were found, except consistently higher mRNA levels of Midkine, p75, and Neurotrophic factor 3 in the preterm cerebellum postnatally, probably reflecting an adaptive response to preterm birth. Pig cerebellar development appears more affected by postconceptional age than by environmental factors at birth or postnatally. Compensatory mechanisms following preterm birth may include faster white matter growth and increased expression of selected genes for neurotrophic factors and regulation of angiogenesis. While the pig cerebellum is immature in 90% gestation preterm pigs, it appears relatively mature and resilient toward environmental factors.

KW - Journal Article

U2 - 10.14814/phy2.12871

DO - 10.14814/phy2.12871

M3 - Journal article

C2 - 27462071

VL - 4

JO - Physiological Reports

JF - Physiological Reports

SN - 2051-817X

IS - 14

M1 - e12871

ER -

ID: 172435520