Insulin resistance in equine digital vessel rings: An in vitro model to study vascular dysfunction in equine laminitis
Article first published online: 15 MAR 2011
© 2011 EVJ Ltd
Equine Veterinary Journal
Volume 43, Issue 6, pages 744–749, November 2011
How to Cite
VENUGOPAL, C. S., EADES, S., HOLMES, E. P. and BEADLE, R. E. (2011), Insulin resistance in equine digital vessel rings: An in vitro model to study vascular dysfunction in equine laminitis. Equine Veterinary Journal, 43: 744–749. doi: 10.1111/j.2042-3306.2010.00351.x
- Issue published online: 11 OCT 2011
- Article first published online: 15 MAR 2011
- [Paper received for publication 26.08.10; Accepted 02.11.10]
- insulin resistance;
- equine laminitis;
- digital vessels;
- in vitro model;
- PI3-kinase blockade
Reasons for performing study: One of the causes of equine laminitis is hyperinsulinaemia, which may be associated with endothelial dysfunction and insulin resistance of vessels.
Hypothesis and objectives: Insulin resistance can be induced in palmar digital vessels by continued exposure to insulin in vitro. The objective was to evaluate this in vitro model for future studies.
Methods: Palmar digital vessel segments were collected immediately after euthanasia from horses with normal insulin/glucose blood values. Four arterial and 4 venous rings (3 mm wide) were prepared and each ring mounted in a tissue bath, containing Tyrode's solution at 37°C, 2 g tension was applied and the rings allowed to equilibrate for 45 min. Of the 4 rings of each vessel type, one was used as a control. One each of the remaining 3 rings was used for incubation with insulin (to induce resistance), wortmannin (to block PI3-kinase) and PD-098059 (to block MAP-kinase), respectively, for 30 min. After the incubation period, the rings were contracted with phenylephrine. When the response reached a plateau, a single dose of insulin was added to the baths and the response of each ring monitored for 30 min.
Results: Insulin relaxed the control rings and those treated with PD 098059 but contracted those pretreated with insulin and wortmannin. Normal relaxation responses of the rings were converted to contractions by insulin resistance. Insulin resistance was confirmed by the qualitative response of insulin-incubated and wortmannin-incubated rings.
Conclusions: This study demonstrated successful induction of insulin resistance in both arterial and venous rings. It also suggested that the MAP-kinase pathway plays a minor role in controlling vasomotor tone under normal physiological conditions.
Potential relevance: The study suggests that the induction of insulin resistance in equine palmar digital vessel rings is reliable and provides a good in vitro model for studying the vascular insulin resistance which may occur in equine laminitis.