# Serum metabolomics identifies metabolic changes in obese cats fed enzymatically hydrolyzed poultry byproduct meal

**Authors:** Leonardo de Andrade Príncipe, Pedro Henrique Marchi, Carolina Dantas Micheletti, João Marcos Bovetto de Campos Valim, Nara Regina Brandão Cônsolo, Raquel Silveira Pedreira, Juliana Toloi Jeremias, Gabriel Henrique Ribeiro, Luiz Alberto Colnago, Julio César de Carvalho Balieiro, Thiago Henrique Annibale Vendramini

PMC · DOI: 10.1093/jvimsj/aalaf075 · Journal of Veterinary Internal Medicine · 2026-01-21

## TL;DR

This study explores how feeding obese cats a specific type of processed poultry meal affects their metabolism, potentially improving energy use.

## Contribution

The study identifies specific metabolic changes in obese cats fed enzymatically hydrolyzed poultry byproduct meal.

## Key findings

- Metabolic changes in valine, acetate, 1-methylhistidine, and glycerol were observed in the test group.
- Pathway analysis showed significant effects on propanoate metabolism, ethanol degradation, fatty acid biosynthesis, and glycerolipid metabolism.
- Findings suggest enhanced fat mobilization and improved branched-chain amino acid utilization in obese cats.

## Abstract

Obesity in cats is a complex metabolic condition, and understanding its metabolic processes is essential for gaining new insights into nutrition.

Investigate the effects of enzymatically-hydrolyzed poultry byproduct meal (EHPM-c) on the serum metabolomic profile of obese cats.

Eighteen adult, neutered, obese domestic cats were enrolled in the study. All subjects underwent comprehensive veterinary evaluations to confirm overall health and rule out concurrent systemic diseases, ensuring a homogenous study population.

Cats were randomized into 2 groups and fed for 45 days with isonutritive diets containing either 30.8% conventional poultry byproduct meal (CPM-c) with 0.0% EHPM-c, or 17.0% CPM-c with 12.0% EHPM-c. After a 30-day diet standardization period, evaluations were performed at baseline (T0) and 45 days (T45) after consumption of the experimental diets. Metabolic spectra were obtained using nuclear magnetic resonance spectroscopy and analyzed using MetaboAnalyst®.

Principal component analysis did not identify differences in the overall metabolite profiles between the groups, but discriminant analysis identified changes in the intensities of valine, acetate, 1-methylhistidine, and glycerol in the test group after 45 days. Additionally, pathway analysis indicated a significant effect on propanoate metabolism, ethanol degradation, fatty acid biosynthesis, and glycerolipid metabolism in the test group.

These findings suggest enhanced fat mobilization and improved utilization of branched-chain amino acids, potentially benefiting energy metabolism in obese cats.

## Linked entities

- **Chemicals:** valine (PubChem CID 1182), acetate (PubChem CID 175), 1-methylhistidine (PubChem CID 64969), glycerol (PubChem CID 753), propanoate (PubChem CID 104745), ethanol (PubChem CID 702)
- **Diseases:** obesity (MONDO:0011122)

## Full-text entities

- **Genes:** Insulin [NCBI Gene 493804], albumin [NCBI Gene 448843], VIP [NCBI Gene 101101640], MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}
- **Diseases:** fat mass (MESH:C536030), metabolic disorders (MESH:D008659), fat (MESH:D004620), hyperthyroidism (MESH:D006980), overweight (MESH:D050177), cachexia (MESH:D002100), Obese (MESH:D009765), diabetes mellitus (MESH:D003920), dyslipidemia (MESH:D050171), FHL (MESH:D051359), chronic diseases (MESH:D002908), urinary tract disease (MESH:D014570), glucose intolerance (MESH:D018149), systemic (MESH:D015619), muscle loss (MESH:D009135), hepatic liposis (MESH:D056486), CHF (MESH:D006333), lean mass loss (MESH:D013851), type 2 diabetes (MESH:D003924), insulin resistance (MESH:D007333), CPM-c (MESH:D030401), weight loss (MESH:D015431), cardiovascular disorders (MESH:D002318), protein (MESH:D011488), hepatic lipidosis (MESH:D008064), excessive (MESH:D006970)
- **Chemicals:** 3-methylhistidine (MESH:C028118), glycine (MESH:D005998), cholesterol (MESH:D002784), ketone bodies (MESH:D007657), ethanol (MESH:D000431), propionyl-CoA (MESH:C009061), kynurenine (MESH:D007737), Copper (MESH:D003300), essential amino acids (MESH:D000601), DL methionine (MESH:D064697), BCAA (MESH:D000597), Biotin (MESH:D001710), vitamin A (MESH:D014801), glycogen (MESH:D006003), Iron (MESH:D007501), acetyl coenzyme A (MESH:D000105), BHT (MESH:D002084), free fatty acids (MESH:D005230), valine (MESH:D014633), phospholipids (MESH:D010743), H2O (MESH:D014867), leucine (MESH:D007930), alanine (MESH:D000409), TCA (MESH:D014233), carbon (MESH:D002244), ketone (MESH:D007659), 2,2-dimethyl-2-silapentane-5-sulfonate (MESH:C009580), triglyceride (MESH:D014280), nitrogen (MESH:D009584), Vitamin E (MESH:D014810), histidine (MESH:D006639), Choline (MESH:D002794), Zinc (MESH:D015032), Sodium chloride (MESH:D012965), proline (MESH:D011392), inosine (MESH:D007288), methionine (MESH:D008715), 3-hydroxybutyrate (MESH:D020155), Folic Acid (MESH:D005492), SCFAs (MESH:D005232), creatinine (MESH:D003404), Manganese (MESH:D008345), glucose (MESH:D005947), acetaldehyde (MESH:D000079), hydrogen (MESH:D006859), tryptophan (MESH:D014364), lysophosphatidylcholines (MESH:D008244), Vitamin B6 (MESH:D025101), Acetate (MESH:D000085), Potassium chloride (MESH:D011189), methylsuccinate (MESH:C041105), N,N-dimethylglycine (MESH:C025138), Iodine (MESH:D007455), Vitamin B12 (MESH:D014805), lipid (MESH:D008055), glutamine (MESH:D005973), Citric acid (MESH:D019343), BHA (MESH:D002083), Pantothenic Acid (MESH:D010205), ATP (MESH:D000255)
- **Species:** Canis lupus familiaris (dog, subspecies) [taxon 9615], Feline leukemia virus (no rank) [taxon 11768], Feline immunodeficiency virus (no rank) [taxon 11673], Homo sapiens (human, species) [taxon 9606], Felis catus (cat, species) [taxon 9685]

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## References

95 references — full list in the complete paper: https://tomesphere.com/paper/PMC12881970/full.md

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Source: https://tomesphere.com/paper/PMC12881970