ArticlePoultry science2026
Integrated analysis of transcriptome and metabolomic uncover molecular mechanisms of ovarian aging in laying hens.
Article in Poultry science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Ovarian aging shortens the productive lifespan and diminishes economic value of poultry, yet its mechanisms are unclear. This study investigated ovarian aging using transcriptomics and metabolomics. Result suggested that the number of primitive, primary, and secondary follicles significantly reduced in aged hens, while atretic follicles increased. Ovaries showed fibrosis with increased collagen deposition, and the thickness of follicle granulosa cell layers was remarkably reduced, exhibiting a disorganized and loose structure. The mitochondria of granulosa cells in aged hens exhibited vacuolation and sparse cristae. Additionally, antioxidant (GSH-Px, SOD) and reproductive hormone (AMH, E2) levels were significantly lower in aged hens (p < 0.05). Transcriptomic analysis revealed altered pathways including PPAR, ECM-receptor interaction, and cytokine-cytokine receptor interaction in aging ovaries. Metabolomic profiling further implicated biosynthesis of unsaturated fatty acids and purine metabolism pathways in aging ovaries. Integrated analysis revealed that FABP4 was a critical mediator linking lipid metabolism and inflammation, and it showed a negative correlation with conjugated linoleic acids (CLA) and cis-4,7,10,13,16,19-docosahexaenoic acid (DHA), suggesting therapeutic potential of their dietary supplementation. To understand how lipid metabolism dysregulation induced ovarian aging, the expression of key genes was assessed by qRT-PCR. The expression of senescence markers (p16, p21, p53), apoptosis-related genes (Bax/Bcl-2) (p < 0.001), autophagy-related gene (p62) (p < 0.01) and inflammation-related genes (IL6, TNFα, NOS2) (p < 0.01) in aged hens signifficantly increased, while the expression of autophagy-related genes (LC3B/LC3A) decreased (p < 0.05). This work provides a theoretical basis for strategies to delay ovarian aging and improve reproductive efficiency.
Indexed as
Identifiers
What Socratic holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.