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Effects of fetal genotype and sex on developmental response to maternal malnutrition

Authors :
Isabel, Beatriz [0000-0001-6192-6411]
García-Contreras, Consolación [0000-0003-4624-2585]
Cogollos, L.
Garcia-Contreras, Consolacion
Vázquez-Gómez, M.
Astiz, Susana
Sánchez Sánchez, Raúl
Gómez Fidalgo, Ernesto
Óvilo Martín, Cristina
Isabel, Beatriz
González De Bulnes, Antonio
Isabel, Beatriz [0000-0001-6192-6411]
García-Contreras, Consolación [0000-0003-4624-2585]
Cogollos, L.
Garcia-Contreras, Consolacion
Vázquez-Gómez, M.
Astiz, Susana
Sánchez Sánchez, Raúl
Gómez Fidalgo, Ernesto
Óvilo Martín, Cristina
Isabel, Beatriz
González De Bulnes, Antonio
Publication Year :
2017

Abstract

The present study aimed to determine whether developmental patterns, adiposity level and fatty-acid composition of fetuses exposed to maternal malnutrition are driven by their sex or their genotype, or both, as these may modulate the adaptive response to the intrauterine environment independently of the maternal genotype. We used a single maternal genotype (purebred Iberian (IB) sows), which was inseminated with heterospermic semen (obtained by mixing semen from Iberian and Large White (LW) boars), to obtain four different subsets of fetuses (male and female, purebred (IB×IB) and crossbred (IB×LW)) in Iberian purebred sows. Analysis of fetal phenotypes indicated a better adaptive response of the female offspring, which was modulated by their genotype. When faced with prenatal undernutrition, females prioritised the growth of vital organs (brain, liver, lungs, kidneys and intestine) at the expense of bone and muscle. Moreover, the analysis of fat composition showed a higher availability of essential fatty acids in the female sex than in their male counterparts and also in the Iberian genotype than in crossbred fetuses. These results are of high translational value for understanding ethnic differences in prenatal programming of postnatal health and disease status, and show evidence that prenatal development and metabolic traits are primarily determined by fetal sex and strongly modulated by fetal genotype. © 2017 CSIRO.

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1373154570
Document Type :
Electronic Resource