ArticleReproductive medicine and biology
Glucose-Induced Developmental Dynamics: Understanding Male Prevalence in Early Mouse Embryo Stages.
Article in Reproductive medicine and biology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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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.
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Who cites it
3 citing papers in PubMed.
- Haploid Parthenotes Have Higher Demand for Glucose and Pyruvate Compared to Normally Fertilized Embryos During their In Vitro Development.Reproductive sciences (Thousand Oaks, Calif.) · 2026Article
- The association of embryo developmental rate and morphological grading with neonatal sex ratio.Scientific reports · 2025Article
- Glucose-Induced Developmental Dynamics: Understanding Male Prevalence in Early Mouse Embryo Stages.Reproductive medicine and biologyArticle
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Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Purpose: Glucose plays a critical role in early embryonic development, influencing metabolic dynamics and developmental competence in a sex-specific manner. This study investigates the complex interplay between glucose availability, developmental competence, and sex-specific outcomes in preimplantation mouse embryos. Methods: Mouse embryos were cultured in a modified KSOM medium with varying glucose concentrations (0-20 mM), monitored via time-lapse microscopy, and analyzed for developmental competence, sex determination by PCR, and X-linked metabolic gene expression. Stage-specific glucose addition/removal experiments and PDHA1 immunofluorescence staining were performed to assess temporal glucose dependency and sex-specific metabolic patterns. Results: Glucose is essential during the morula-to-blastocyst transition. Analysis of developmental dynamics showed that glucose concentration affected the variability in developmental rates, particularly at the four-cell and eight-cell stages. Interestingly, sex ratio skewing was observed, with male embryos dominating the early developmental groups regardless of glucose levels. Expression analysis of X-linked metabolic genes revealed stage-specific patterns, with PDHA1 exhibiting the highest activity at the eight-cell stage. Conclusions: Glucose availability accelerated embryonic development and created sex-specific patterns of developmental timing, with male embryos exhibiting faster progression rates, which might be associated with differential X-linked PDHA1 metabolic gene expression during early mouse embryogenesis.
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