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Glucose concentration during equine in vitro maturation alters mitochondrial function
Niamh Lewis1, Katrin Hinrichs2, Henry J Leese3
1Institute of Ageing and Chronic Disease, University of Liverpool, Cheshire, UK.
High glucose concentrations during equine oocyte maturation negatively impact mitochondrial function and gene expression, despite similar maturation and blastocyst rates. Further research is needed to assess developmental outcomes.
Area of Science:
- Animal Science
- Reproductive Biology
- Biochemistry
Background:
- In vitro embryo production in horses is growing, but protocols require optimization.
- Common in vitro maturation (IVM) media use differing glucose concentrations (5.6 mM vs. 17 mM).
- High glucose effects on equine oocytes are unknown, unlike in other mammals.
Purpose of the Study:
- To investigate the impact of physiological (5.6 mM) versus supraphysiological (17 mM) glucose concentrations during equine IVM on oocyte energy metabolism and gene expression.
- To compare mitochondrial function and key metabolic gene expression in equine oocytes and cumulus cells matured under different glucose conditions.
Main Methods:
- Equine cumulus-oocyte complexes (COCs) were matured in M199 with either 5.6 mM or 17 mM glucose.
- Spent media analyzed for glucose consumption, lactate, and pyruvate.
- Mitochondrial function assessed via respirometry.
- Expression of lactate dehydrogenase-A (LDHA) analyzed in cumulus cells.
Main Results:
- No significant differences in COC glucose consumption, lactate, or pyruvate production between groups.
- A decreased glycolytic index observed at 17 mM glucose.
- IVM in 17 mM glucose led to reduced ATP-coupled respiration and increased non-mitochondrial respiration.
- LDHA was downregulated in cumulus cells matured with 17 mM glucose.
- Maturation and blastocyst rates remained unaffected by glucose concentration.
Conclusions:
- Supraphysiological glucose (17 mM) during equine IVM alters COC mitochondrial function and LDHA gene expression.
- These metabolic changes occur without affecting maturation or blastocyst rates.
- Further investigation is required to determine the long-term developmental consequences for offspring.
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