Sexual Dimorphism in Placental mTORC1 Signaling, Amino Acid Transport, and Mitochondrial Respiration at Term.
What this study shows
In 46 term placentas, male placentas showed higher mTORC1 signalling (increased S6RP phosphorylation, reduced 4E-BP1), greater System A amino acid transport and higher mitochondrial respiratory capacity than female placentas, and male pregnancies had a higher birth-weight-to-placental-weight ratio. Observational: a cross-sectional association at a single timepoint, with no intervention and no randomisation, so the direction of the relationship between mTORC1 signalling and growth is not established here and residual confounding by maternal and obstetric factors cannot be excluded.
At a glance
| Evidence type | H Human study Marked H because it is direct evidence from a human clinical trial or human cohort; the code names the kind of study, not its quality -- a small, well-run trial is still H. |
| Study type | 3 - Human Observational |
| Model system | Human placenta at term (n=46) |
| Journal | Antioxidants |
| Year | 2026 |
| Peer reviewed | Yes |
| Record last updated | 2026-10-01 |
| Source | DOI 10.3390/antiox15080977 · PMID 42650242 · Free full text (PMC13509233) |
Extracted findings
These fields were extracted from the paper with AI assistance and have not been checked against the source. Read them as a pointer into the paper, not as curated claims; where they disagree with the curated summary above, the curated summary stands.
| Intervention | None (observational comparison by fetal sex) |
| Target | mTORC1; S6RP; 4E-BP1; System A amino acid transport |
| Model | Human |
| Effect | Higher mTORC1 activity, amino acid transport and mitochondrial respiratory capacity in male placentas; higher birth-weight-to-placental-weight ratio |
In the Atlas
Related topics
More studies on this topic
- mTOR controls mitochondrial oxidative function through a YY1-PGC-1alpha transcriptional complex (2007)
- L-Arginine Modulates T Cell Metabolism and Enhances Survival and Anti-tumor Activity (2016)
- mTORC1 controls mitochondrial activity and biogenesis through 4E-BP-dependent translational regulation (2013)
- The mammalian target of rapamycin (mTOR) pathway regulates mitochondrial oxygen consumption and oxidative capacity (2006)
Thank you. Your answer was counted anonymously.