# Performing Dual Glucose Clamp Experiments in Sedated Farm Swine: A Practical Method

**Authors:** Marc C. Torjman, Winston C. Hamilton, Katherine Dillon, Channy Loeum, Jeffrey I. Joseph

PMC · DOI: 10.3390/mps8050118 · Methods and Protocols · 2025-10-02

## TL;DR

This paper describes a practical method for performing glucose clamp experiments in sedated farm swine, which could reduce the number of animals needed for such studies.

## Contribution

A new method for conducting dual glucose clamp experiments in sedated farm swine using customized equipment and procedures.

## Key findings

- The method successfully maintained blood glucose levels within a narrow range during 24 experiments.
- Infusaports remained functional for over 700 blood draws per animal without signs of infection.
- The protocol was effective and animals remained healthy throughout the study.

## Abstract

The hyperinsulinemic–euglycemic clamp technique is considered the gold standard for measuring insulin sensitivity in large animals. We developed a practical method for conducting concurrent glucose clamp experiments in a pair of sedated farm swine positioned in a sling. Descriptions of customized equipment and central venous access surgical procedures for blood collection are provided. Personnel functions are described for execution of the clamp protocol. A total of 24 hyperinsulinemic–euglycemic clamp studies were performed over 6 weeks. Infusaports remained functional for 1454 blood samples. There were three CSII catheter occlusions during bolus administration, and the swine showed no signs of infection or disease. IM telazol at 1.0 mg/kg, administered 1–2 h prior (mean of 3.26 mL ± 1.59) was effective in keeping animals comfortable. SpO2 and heart rate remained within normal ranges. Means ± SD total infused volumes for octreotide, 10% dextrose, and saline were 9.7 ± 0.93 mL, 2328.0 ± 672.8 mL, and 690.3 ± 206.8 mL. Mean blood glucose was maintained between 75.7 and 87.8 mg/dL (CV 3.17%) for the 24 experiments. The GIR infusion rate peaked between 15 and 60 min after insulin bolusing, with insulin Cmax of 108.5 pmol/L and tmax at 10 min. All aspects of the protocol were effectively carried out. The animals remained in good health, and the implanted infusion ports remained patent for over 700 blood draws per animal. This method could potentially reduce the number of animals used and the costs of other similar experiments.

## Linked entities

- **Chemicals:** octreotide (PubChem CID 448601), 10% dextrose (PubChem CID 22814120), saline (PubChem CID 5234)

## Full-text entities

- **Genes:** INS (insulin) [NCBI Gene 397415]
- **Diseases:** hyperinsulinemic-euglycemic (MESH:D044903), infection (MESH:D007239)
- **Chemicals:** Glucose (MESH:D005947), telazol (MESH:C006131), CSII (-), blood glucose (MESH:D001786), octreotide (MESH:D015282)
- **Species:** Sus scrofa (pig, species) [taxon 9823]

## Full text

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## Figures

11 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12567051/full.md

## References

21 references — full list in the complete paper: https://tomesphere.com/paper/PMC12567051/full.md

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Source: https://tomesphere.com/paper/PMC12567051