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Asymmetric growth-limiting development of the female conceptus.

Authors :
Estrella CAS
Gatford KL
Xiang R
Javadmanesh A
Ghanipoor-Samami M
Nattrass GS
Shuaib E
McAllister MM
Beckman I
Thomsen DA
Clifton VL
Owens JA
Roberts CT
Hiendleder S
Kind KL
Source :
Frontiers in endocrinology [Front Endocrinol (Lausanne)] 2024 Feb 01; Vol. 14, pp. 1306513. Date of Electronic Publication: 2024 Feb 01 (Print Publication: 2023).
Publication Year :
2024

Abstract

Introduction: Sex differences in prenatal growth may contribute to sex-dependent programming effects on postnatal phenotype.<br />Methods: We integrated for the first time phenotypic, histomorphological, clinico-chemical, endocrine and gene expression analyses in a single species, the bovine conceptus at mid-gestation.<br />Results: We demonstrate that by mid-gestation, before the onset of accelerated growth, the female conceptus displays asymmetric lower growth compared to males. Female fetuses were smaller with lower ponderal index and organ weights than males. However, their brain:body weight, brain:liver weight and heart:body weight ratios were higher than in males, indicating brain and heart 'sparing'. The female placenta weighed less and had lower volumes of trophoblast and fetal connective tissue than the male placenta. Female umbilical cord vessel diameters were smaller, and female-specific relationships of body weight and brain:liver weight ratios with cord vessel diameters indicated that the umbilico-placental vascular system creates a growth-limiting environment where blood flow is redistributed to protect brain and heart growth. Clinico-chemical indicators of liver perfusion support this female-specific growth-limiting phenotype, while lower insulin-like growth factor 2 (IGF2) gene expression in brain and heart, and lower circulating IGF2, implicate female-specific modulation of key endocrine mediators by nutrient supply.<br />Conclusion: This mode of female development may increase resilience to environmental perturbations in utero and contribute to sex-bias in programming outcomes including susceptibility to non-communicable diseases.<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2024 Estrella, Gatford, Xiang, Javadmanesh, Ghanipoor-Samami, Nattrass, Shuaib, McAllister, Beckman, Thomsen, Clifton, Owens, Roberts, Hiendleder and Kind.)

Details

Language :
English
ISSN :
1664-2392
Volume :
14
Database :
MEDLINE
Journal :
Frontiers in endocrinology
Publication Type :
Academic Journal
Accession number :
38362586
Full Text :
https://doi.org/10.3389/fendo.2023.1306513