# Feeding butter with elevated content of trans-10, cis-12 conjugated linoleic acid to obese-prone rats impairs glucose and insulin tolerance

**Authors:** Melissa Hamilton, Loren E. Hopkins, Ousama AlZahal, Tara L. MacDonald, Daniel T. Cervone, David C. Wright, Brian W. McBride, David J. Dyck

PMC · DOI: 10.1186/s12944-015-0122-2 · Lipids in Health and Disease · 2015-09-28

## TL;DR

Feeding rats a butter enriched with a specific type of fat worsened their blood sugar and insulin control, even without changes in activity or weight.

## Contribution

Demonstrates that trans-10, cis-12 conjugated linoleic acid in butter impairs glucose and insulin tolerance in diabetes-prone rats.

## Key findings

- Glucose and insulin tolerance were most impaired in rats fed lard or SARA butter.
- Insulin signaling was impaired in multiple tissues but did not differ between diets.
- Physical activity and energy expenditure did not explain the metabolic impairments.

## Abstract

We recently demonstrated that feeding a natural CLAt10,c12-enriched butter to lean female rats resulted in small, but significant increases in fasting glucose and insulin concentrations, and impaired insulin tolerance. Our goal was to extend these findings by utilizing the diabetes-prone female fatty Zucker rat. Rats were fed custom diets containing 45 % kcal of fat derived from control and CLAt10,c12-enriched butter for 8 weeks.

CLA t10,c12-enriched butter was prepared from milk collected from cows fed a high fermentable carbohydrate diet to create subacute rumen acidosis (SARA); control (non-SARA) butter was collected from cows fed a low grain diet. Female fatty Zucker rats (10 weeks old) were randomly assigned to one of four diet treatments: i) low fat (10 % kcal), ii) 45 % kcal lard, iii) 45 % kcal SARA butter, or iv) 45 % kcal non-SARA butter. A low fat fed lean Zucker group was used as a control group. After 8 weeks, i) glucose and insulin tolerance tests, ii) insulin signaling in muscle, adipose and liver, and iii) metabolic caging measurements were performed.

Glucose and insulin tolerance were significantly impaired in all fatty Zucker groups, but to the greatest extent in the LARD and SARA conditions. Insulin signaling (AKT phosphorylation) was impaired in muscle, visceral (perigonadal) adipose tissue and liver in fatty Zucker rats, but was generally similar across dietary groups. Physical activity, oxygen consumption, food intake and weight gain were also similar amongst the various fatty Zucker groups.

Increasing the consumption of a food naturally enriched with CLAt10,c12 significantly worsens glucose and insulin tolerance in a diabetes-prone rodent model. This outcome is not explained by changes in tissue insulin signaling, physical activity, energy expenditure, food intake or body mass.

## Linked entities

- **Proteins:** AKT1 (AKT serine/threonine kinase 1)
- **Chemicals:** trans-10, cis-12 conjugated linoleic acid (PubChem CID 5282800)
- **Diseases:** diabetes (MONDO:0005015)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, Akt1 (AKT serine/threonine kinase 1) [NCBI Gene 24185] {aka Akt}
- **Diseases:** WG (MESH:D014890), SARA (MESH:D000138), lipoatrophic condition (MESH:D052496), weight loss (MESH:D015431), Diabetes (MESH:D003920), inflammation (MESH:D007249), insulin intolerance (MESH:D007333), overweight (MESH:D050177), fatty (MESH:D008067), impaired glucose and insulin tolerance (MESH:D018149), obese (MESH:D009765), hyperinsulinemia (MESH:D006946), weight gain (MESH:D015430), OA (MESH:D010003)
- **Species:** Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116], Bos taurus (bovine, species) [taxon 9913], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC4587826/full.md

## References

22 references — full list in the complete paper: https://tomesphere.com/paper/PMC4587826/full.md

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Source: https://tomesphere.com/paper/PMC4587826