Controlled elevated temperatures during early-mid gestation cause placental insufficiency and implications for fetal growth in pregnant pigs.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
26 11 2020
Historique:
received: 20 02 2020
accepted: 10 11 2020
entrez: 27 11 2020
pubmed: 28 11 2020
medline: 18 3 2021
Statut: epublish

Résumé

It is known that pig offspring born from pregnant pigs exposed to elevated ambient temperatures during gestation have altered phenotypes, possibly due to placental insufficiency and impaired fetal growth. Therefore, the objective of this study was to quantify the effect of maternal heat exposure during early-mid gestation, when pig placentae grow heavily, on placental and fetal development. Fifteen pregnant pigs were allocated to thermoneutral (TN; 20 °C; n = 7) or cyclic elevated temperature conditions (ET; 28 to 33 °C; n = 8) from d40 to d60 of gestation. Following euthanasia of the pigs on d60, placental and fetal morphometry and biochemistry were measured. Compared to TN fetuses, ET fetuses had increased (P = 0.041) placental weights and a lower (P = 0.013) placental efficiency (fetal/placental weight), although fetal weights were not significantly different. Fetuses from ET pigs had reduced (P = 0.032) M. longissimus fibre number density and a thicker (P = 0.017) placental epithelial layer compared to their TN counterparts. Elevated temperatures decreased (P = 0.026) placental mRNA expression of a glucose transporter (GLUT-3) and increased (P = 0.037) placental IGF-2 mRNA expression. In conclusion, controlled elevated temperatures between d40 to d60 of gestation reduced pig placental efficiency, resulting in compensatory growth of the placentae to maintain fetal development. Placental insufficiency during early-mid gestation may have implications for fetal development, possibly causing a long-term phenotypic change of the progeny.

Identifiants

pubmed: 33244103
doi: 10.1038/s41598-020-77647-1
pii: 10.1038/s41598-020-77647-1
pmc: PMC7691357
doi:

Substances chimiques

Glucose Transporter Type 3 0
RNA, Messenger 0
Insulin-Like Growth Factor II 67763-97-7

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

20677

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Auteurs

Weicheng Zhao (W)

Faculty of Veterinary and Agricultural Sciences, University of Melbourne, Parkville, 3010, Australia.

Fan Liu (F)

Rivalea Australia Pty Ltd, Corowa, 2646, Australia.

Alan W Bell (AW)

Department of Animal Science, Cornell University, Ithaca, 14853-4801, USA.

Hieu H Le (HH)

Faculty of Veterinary and Agricultural Sciences, University of Melbourne, Parkville, 3010, Australia.

Jeremy J Cottrell (JJ)

Faculty of Veterinary and Agricultural Sciences, University of Melbourne, Parkville, 3010, Australia.

Brian J Leury (BJ)

Faculty of Veterinary and Agricultural Sciences, University of Melbourne, Parkville, 3010, Australia.

Mark P Green (MP)

School of BioSciences, University of Melbourne, Parkville, 3010, Australia.

Frank R Dunshea (FR)

Faculty of Veterinary and Agricultural Sciences, University of Melbourne, Parkville, 3010, Australia. fdunshea@unimelb.edu.au.
Faculty of Biological Sciences, The University of Leeds, Leeds, LS2 9JT, United Kingdom. fdunshea@unimelb.edu.au.

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