# Circulating lipid profiles and post-prandial glucose and insulin in response to dietary macronutrient composition in lean and obese cats

**Authors:** Hannah Godfrey, Érico M Ribeiro, Shoshana Verton-Shaw, Anna Kate Shoveller, Darcia Kostiuk, Janelle Kelly, Jennifer Saunders Blades, Ron Johnson, Adronie Verbrugghe

PMC · DOI: 10.1093/jvimsj/aalag013 · Journal of Veterinary Internal Medicine · 2026-02-17

## TL;DR

This study shows how different diets affect insulin and lipid levels in lean and obese cats, highlighting the role of protein in metabolic responses.

## Contribution

The study reveals the metabolic flexibility of cats and the impact of protein content in diets on insulin responses.

## Key findings

- The low-protein diet led to lower post-prandial insulin concentrations compared to low-fat and low-carbohydrate diets.
- The low-fat diet reduced fasted cholesterol and LDL-c levels compared to other diets.
- No significant differences in lipid profiles were found between lean and obese cats.

## Abstract

Insulin response to a meal is crucial for metabolic health in cats, influencing the risk of metabolic disorders.

Investigate dietary macronutrient compositions on fasted and post-prandial insulin and glucose responses, and lipid profiles, in lean and obese cats.

Nine lean and 9 obese, male neutered colony cats.

Cats were fed 3 extruded dry diets: low protein (LP: 28% protein, 40% fat, and 32% nitrogen-free extract [NFE]), low fat (LF: 40% protein, 30% fat, and 30% NFE), and low carbohydrate (LC: 36% protein, 41% fat, and 23% NFE) for 28 days using a 3 × 3 Latin square design. Fasted and post-prandial blood samples were collected to measure serum insulin and whole blood glucose concentrations, and fasted samples were analyzed for serum cholesterol, triacylglycerol (TAG), nonesterified fatty acid (NEFA), very low-density lipoprotein (VLDL), low-density lipoprotein cholesterol (LDL-c), and high-density lipoprotein cholesterol (HDL-c) concentrations at the end of each period.

No differences were found in serum insulin, glucose, cholesterol, NEFA, TAG, HDL-c, LDL-c, or VLDL concentrations between lean and obese cats (P > .05) suggesting dyslipidemia was not present in the obese cats. The LP diet resulted in lower post-prandial insulin concentrations compared with the LC and LF diets (P = .01) which was attributed to lower protein intake with the LP diet. As expected, the LF diet led to lower fasted serum cholesterol and LDL-c concentrations compared with the LP and LC diets (P < .001).

These findings document the metabolic flexibility of cats and suggest that dietary macronutrient composition, particularly protein content, plays an important role in modulating insulin responses in adult, otherwise healthy, cats.

## Full-text entities

- **Genes:** Leptin [NCBI Gene 493838], lipoprotein lipase [NCBI Gene 727696], PYY [NCBI Gene 105261189], Insulin [NCBI Gene 493804]
- **Diseases:** iAUC (MESH:D001927), hyperglycemic (MESH:D006944), hyperinsulinemia (MESH:D006946), insulin resistance (MESH:D007333), type II diabetes (MESH:D003924), Impaired glucose tolerance (MESH:D018149), dyslipidemia (MESH:D050171), hyperglycemia (MESH:D006943), metabolic syndrome (MESH:D024821), IR (MESH:C537629), inflammation (MESH:D007249), DM (MESH:D009223), BCS (MESH:D057215), diabetic (MESH:D003920), beta-cell failure (MESH:D051437), overweight (MESH:D050177), Obese (MESH:D009765), metabolic disorders (MESH:D008659)
- **Chemicals:** AUCIns (-), Carbohydrate (MESH:D002241), cholesterol-esters (MESH:D002788), corn starch (MESH:D013213), amino acid (MESH:D000596), Dexdomitor (MESH:D020927), LP (MESH:D008070), lipid (MESH:D008055), Glucose (MESH:D005947), Ins (MESH:D007204), amylose (MESH:D000688), fat (MESH:D005223), TAG (MESH:D014280), nitrogen (MESH:D009584), atipamezole (MESH:C050701), FFA (MESH:D005230), butorphanol (MESH:D002077), glycogen (MESH:D006003), water (MESH:D014867), blood glucose (MESH:D001786), cholesterol (MESH:D002784), Glu (MESH:D018698), propofol (MESH:D015742)
- **Species:** Powellomyces sp. EA (species) [taxon 252690], Felis catus (cat, species) [taxon 9685], Homo sapiens (human, species) [taxon 9606], Rodentia (rodent, order) [taxon 9989], Canis lupus familiaris (dog, subspecies) [taxon 9615]

## Full text

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## Figures

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## References

90 references — full list in the complete paper: https://tomesphere.com/paper/PMC12910623/full.md

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Source: https://tomesphere.com/paper/PMC12910623