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Updated: Feb 3, 2026

Hyperpolarized 13C Metabolic Magnetic Resonance Spectroscopy and Imaging
Published on: December 30, 2016
Probing human sperm metabolism using 13C-magnetic resonance spectroscopy
S J Calvert1, S Reynolds2, M N Paley2
1Academic Unit of Reproductive & Developmental Medicine, Department of Oncology and Metabolism, University of Sheffield, Level 4, The Jessop Wing, Tree Root Walk, Sheffield, UK.
13C-Magnetic Resonance Spectroscopy (MRS) reveals human sperm metabolism, showing vital sperm utilize glucose more efficiently for energy. This non-destructive assay could lead to improved fertility treatments by detecting metabolic dysfunction.
Area of Science:
- Biochemistry
- Metabolomics
- Reproductive Biology
Background:
- Human sperm energy production pathways, glycolysis and oxidative phosphorylation, are debated.
- Previous studies on sperm metabolism lacked detailed metabolic analysis.
Purpose of the Study:
- To investigate human sperm metabolism using 13C-Magnetic Resonance Spectroscopy (MRS).
- To determine substrate utilization by different human sperm populations.
- To assess the feasibility of using 13C-MRS for non-destructive sperm analysis.
Main Methods:
- Human sperm populations were isolated using density gradient centrifugation (DGC).
- Sperm were incubated with 13C-labelled substrates (glucose, fructose, pyruvate).
- Metabolism was analyzed via 1D 13C MRS, quantifying lactate and bicarbonate production.
Main Results:
- 13C-labelled glucose, fructose, and pyruvate were converted to lactate and bicarbonate.
- Vital and motile sperm from the 40/80% interface showed significantly higher glucose conversion to lactate compared to pellet sperm.
- Lactate production correlated with sperm concentration but not non-sperm cells.
Conclusions:
- 13C-MRS is a viable tool for assessing human sperm metabolism.
- Vital sperm demonstrate preferential glucose utilization, suggesting distinct metabolic strategies.
- This method holds potential for diagnosing and treating male infertility by identifying metabolic deficits.
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