# Metabolomics and Lipidomics in the Study of Reproductive Performance in Livestock

**Authors:** Zhengmei Sheng, Yuyang Gao, Yuqing Chong, Ying Lu, Jinpeng Shi, Huaijing Liu, Keyu Li, Weidong Deng, Jiao Wu

PMC · DOI: 10.3390/ani16040588 · Animals : an Open Access Journal from MDPI · 2026-02-12

## TL;DR

This review explores how metabolomics and lipidomics help understand and improve livestock reproduction by linking metabolism and epigenetics.

## Contribution

The paper provides a comprehensive review of metabolic-epigenetic interactions in livestock reproduction and their implications for fertility improvement.

## Key findings

- Metabolic pathways like glycolysis and lipid metabolism interact with epigenetic mechanisms to regulate reproductive processes.
- Metabolomics and lipidomics reveal biomarkers in semen, follicular fluid, and embryos that correlate with fertility.
- Nutritional interventions and reproductive technologies can be optimized using insights from metabolic and lipid profiles.

## Abstract

Reproductive efficiency is a critical factor for livestock productivity and sustainability. Recent evidence shows that metabolism not only provides energy for reproduction but also regulates gene expression through epigenetic modifications. This metabolic–epigenetic coupling affects gamete quality, embryo development, implantation, and pregnancy maintenance, but its coordination across reproductive stages is not fully understood. In this review, we summarize knowledge on metabolic–epigenetic interactions in cattle, sheep, pigs, and poultry. We focus on how metabolic pathways like glycolysis, lipid metabolism, and one-carbon metabolism interact with DNA methylation, histone modifications, and non-coding RNAs to regulate reproduction. Understanding these interactions opens new opportunities to improve fertility through nutrition, biomarker selection, and reproductive technologies, providing a framework to enhance livestock reproductive efficiency.

With the rapid development of omics technologies, metabolomics and lipidomics have become important tools for elucidating the molecular basis of reproductive performance in livestock. These approaches, which focus on small metabolites and lipid species, provide valuable insights into dynamic interactions between genes, proteins, and the environment, offering a high level of sensitivity. This review summarizes key methodological advances in metabolomics and lipidomics and their applications to gametogenesis, oocyte maturation, embryo development, and pregnancy maintenance. It highlights how metabolic and lipid pathways, particularly those involving energy metabolism, redox regulation, lipid remodeling, and cell–cell signaling, affect reproductive cell quality. This review further integrates biomarkers identified from semen, follicular fluid, oocytes, embryos, and uterine tissues, highlighting their potential roles in fertility assessment. Together, these insights enhance our understanding of metabolic regulation in reproduction and support the effective application of metabolomics and lipidomics in improving livestock fertility.

## Full-text entities

- **Genes:** ELOVL6 (ELOVL fatty acid elongase 6) [NCBI Gene 533333], GK (glycerol kinase) [NCBI Gene 505987], MYRF (myelin regulatory factor) [NCBI Gene 509704] {aka C29H11orf9}, EGR1 (early growth response 1) [NCBI Gene 407125], STRA8 (stimulated by retinoic acid 8) [NCBI Gene 785714] {aka STRA8-like}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 280991] {aka AKT}, BBOX1 (gamma-butyrobetaine hydroxylase 1) [NCBI Gene 507159], TGFB2 (transforming growth factor beta 2) [NCBI Gene 534069] {aka MGF}, SLC25A39 (solute carrier family 25 member 39) [NCBI Gene 509684], PIK3CA (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha) [NCBI Gene 282306], CYC1 (cytochrome c1) [NCBI Gene 512500], PDHA2 (pyruvate dehydrogenase E1 subunit alpha 2) [NCBI Gene 768012], GNAI1 (G protein subunit alpha i1) [NCBI Gene 281790] {aka HG1B}, RBP4 (retinol binding protein 4) [NCBI Gene 281444], TJP1 (tight junction protein 1) [NCBI Gene 407102] {aka zo1}, MIR100 (microRNA mir-100) [NCBI Gene 100313483] {aka bta-mir-100, mir-100}, NDUFS8 (NADH:ubiquinone oxidoreductase core subunit S8) [NCBI Gene 287027], ADAMTS1 (ADAM metallopeptidase with thrombospondin type 1 motif 1) [NCBI Gene 512171], CDK1 (cyclin dependent kinase 1) [NCBI Gene 281061] {aka CDC2}, BHMT (betaine--homocysteine S-methyltransferase) [NCBI Gene 497025], EGFR (epidermal growth factor receptor) [NCBI Gene 407217], SYCP3 (synaptonemal complex protein 3) [NCBI Gene 615896], HMOX2 (heme oxygenase 2) [NCBI Gene 510243], GGT7 (gamma-glutamyltransferase 7) [NCBI Gene 615929] {aka GGTL3}, STAR (steroidogenic acute regulatory protein) [NCBI Gene 281507], KISS1R (KISS1 receptor) [NCBI Gene 528699] {aka GPR54}, ANG (angiogenin, ribonuclease, RNase A family, 5) [NCBI Gene 777597] {aka ANG1, RAA1}, PLAU (plasminogen activator, urokinase) [NCBI Gene 281408], GPAM (glycerol-3-phosphate acyltransferase, mitochondrial) [NCBI Gene 497202], PARK7 (Parkinsonism associated deglycase) [NCBI Gene 511268] {aka DJ-1, DJ1}, GGA1 (golgi associated, gamma adaptin ear containing, ARF binding protein 1) [NCBI Gene 534634], FOS (Fos proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 280795], BMP15 (bone morphogenetic protein 15) [NCBI Gene 353351] {aka bmp-15}, PDE3A (phosphodiesterase 3A) [NCBI Gene 536636], MIF (macrophage migration inhibitory factor) [NCBI Gene 280858], DHFR (dihydrofolate reductase) [NCBI Gene 508809], CYP19A1 (cytochrome P450 family 19 subfamily A member 1) [NCBI Gene 281740] {aka CYP19, CYP19P1}, CCNB1 (cyclin B1) [NCBI Gene 327679], FSHR (follicle stimulating hormone receptor) [NCBI Gene 281172], GDF9 (growth differentiation factor 9) [NCBI Gene 282574], MIR10B (microRNA mir-10b) [NCBI Gene 791051] {aka MIRN10B, bta-mir-10b, mir-10b}, CPEB3 (cytoplasmic polyadenylation element binding protein 3) [NCBI Gene 537016], G6PD (glucose-6-phosphate dehydrogenase) [NCBI Gene 281179], LPAR1 (lysophosphatidic acid receptor 1) [NCBI Gene 281136] {aka EDG2}, IDH3G (isocitrate dehydrogenase (NAD(+)) 3 non-catalytic subunit gamma) [NCBI Gene 614145], LDH (Muscle lactate dehydrogenase activity) [NCBI Gene 101409728], NDUFA4 (NDUFA4 mitochondrial complex associated) [NCBI Gene 327704] {aka COXFA4}, MAP3K1 (mitogen-activated protein kinase kinase kinase 1) [NCBI Gene 523962], PLAUR (plasminogen activator, urokinase receptor) [NCBI Gene 281983], CASP3 (caspase 3) [NCBI Gene 408016], PEG10 (paternally expressed 10) [NCBI Gene 618138], KISS1 (KiSS-1 metastasis suppressor) [NCBI Gene 615613], PCK1 (phosphoenolpyruvate carboxykinase 1) [NCBI Gene 282855] {aka PPCK1}, SOD1 (superoxide dismutase 1) [NCBI Gene 281495] {aka SOD1L1}, MSTN (myostatin) [NCBI Gene 281187] {aka GDF8}, UTRN (utrophin) [NCBI Gene 534358], AGO2 (argonaute RISC catalytic component 2) [NCBI Gene 404130] {aka EIF2C2}, CS (citrate synthase) [NCBI Gene 280682], IDUA (alpha-L-iduronidase) [NCBI Gene 511050], RSPO2 (R-spondin 2) [NCBI Gene 536121]
- **Diseases:** injury to (MESH:D014947), inflammation (MESH:D007249), methionine (MESH:C565394), embryonic loss (MESH:D020964), spermatogenesis disorders (MESH:C536875), reproductive failure (MESH:D051437), fetal overgrowth syndrome (MESH:D005315), ovarian dysfunction (MESH:D010049), hypoxia (MESH:D000860)
- **Chemicals:** Melatonin (MESH:D008550), bile acid (MESH:D001647), methionine (MESH:D008715), pyruvate (MESH:D019289), D-proline (-), adenosine (MESH:D000241), succinate (MESH:D019802), L-carnitine (MESH:D002331), betaine (MESH:D001622), BAIBA (MESH:C033435), RA (MESH:D014212), PUFA (MESH:D005231), alpha-KG (MESH:D007656), choline (MESH:D002794), cortisol (MESH:D006854), prostaglandin (MESH:D011453), Hcy (MESH:D006710), Amino acid (MESH:D000596), lactate (MESH:D019344), estradiol (MESH:D004958), carbon (MESH:D002244), phosphatidylserine (MESH:D010718), pentose phosphate (MESH:D010428), fatty acid (MESH:D005227), carbohydrates (MESH:D002241), phosphatidylcholine (MESH:D010713), alanine (MESH:D000409), TCA (MESH:D014238), cholesterol esters (MESH:D002788), serine (MESH:D012694), alpha-linolenic acid (MESH:D017962), GSH (MESH:D005978), steroid (MESH:D013256), kaempferol (MESH:C006552), glutamine (MESH:D005973), beta-alanine (MESH:D015091), leucine (MESH:D007930), cis-9, trans-11 conjugated linoleic acid (MESH:C503589), polyamine (MESH:D011073), ATP (MESH:D000255), phospholipids (MESH:D010743), S-adenosylmethionine (MESH:D012436), endocannabinoids (MESH:D063388), retinol (MESH:D014801), testosterone (MESH:D013739), Acetyl-CoA (MESH:D000105), arachidonic acid (MESH:D016718), cysteine (MESH:D003545), Lipid (MESH:D008055), L-homocitrulline (MESH:C001352), LH (MESH:D007986), L-citrulline (MESH:D002956), L-tryptophan (MESH:D014364), diglycerides (MESH:D004075), progesterone (MESH:D011374), glutamate (MESH:D018698), prostaglandin I2 (MESH:D011464), acetylcarnitine (MESH:D000108), sphingolipids (MESH:D013107), NAD+ (MESH:D009243)
- **Species:** Akkermansia muciniphila (species) [taxon 239935], Homo sapiens (human, species) [taxon 9606], Bos taurus (bovine, species) [taxon 9913], Ovis aries (domestic sheep, species) [taxon 9940], Bos indicus (Indicine cattle, species) [taxon 9915], Sus scrofa (pig, species) [taxon 9823], Gallus gallus (bantam, species) [taxon 9031], gut metagenome (species) [taxon 749906], Capra hircus (domestic goat, species) [taxon 9925], Anas platyrhynchos (duck, species) [taxon 8839]

## Full text

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## Figures

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## References

134 references — full list in the complete paper: https://tomesphere.com/paper/PMC12937480/full.md

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Source: https://tomesphere.com/paper/PMC12937480