In vitro reactivity of digital arteries and veins to vasoconstrictive mediators in healthy horses and in horses with early laminitis.
Abstract: The in vitro reactivity of vasoconstrictive mediators that are implicated in acute laminitis was determined in palmar and plantar digital arteries and veins obtained from healthy horses and in palmar digital vessels of horses with early laminitis (Obel grade I). To obtain baseline reactivity data, 3 experiments were conducted, using healthy horses: (1) the reactivity of palmar and plantar digital arteries and veins to angiotensin II, norepinephrine, and 5-hydroxytryptamine (serotonin) were compared; (2) the direct effects of bacterial endotoxin on vascular reactivity were assessed; and (3) the reactivity of palmar digital arteries and veins to angiotensin II, norepinephrine, prostaglandin F2 alpha (PGF2 alpha), serotonin, and a thromboxane-endoperoxide analog (U46619) were determined. The vascular reactivity of these same 5 vasoconstrictors then was determined in horses with early laminitis and was compared with data from healthy (control) horses. Obel grade-I laminitis was experimentally induced in horses, using carbohydrate overload. Dose responses were conducted for each agent at concentrations between 10(-8)M and 10(-4)M. The potency of a drug was defined as the mean effective concentration necessary to induce 50% of maximal contraction (EC50). There were no differences in EC50 concentrations and in maximal contractions between forelimb and hind limb arteries and veins for angiotensin II, norepinephrine, and serotonin. Incubation with endotoxin had no effect on the reactivity of arteries and veins to angiotensin II, norepinephrine, and serotonin.(ABSTRACT TRUNCATED AT 250 WORDS)
Publication Date: 1989-04-01 PubMed ID: 2712417
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- Comparative Study
- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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The research article focuses on studying how certain substances involved in the blood vessel narrowing process react in healthy horses versus horses in the early stages of laminitis, a painful and potentially crippling disease.
Objectives of the Research
- The main aim of the research is to study the in vitro reactivity of vasoconstrictive elements – substances that cause blood vessels to narrow – that are known to be implicated in acute laminitis.
- This is compared between tissues taken from healthy horses and tissues taken from horses showing early signs of laminitis (Obel grade I).
Experiments and procedures
- The researchers conducted three experiments all using healthy horses to gather baseline data on vascular reactivity.
- The first experiment compared the way palmar and plantar digital arteries and veins reacted to angiotensin II, norepinephrine, and serotonin – all substances known to cause vasoconstriction.
- The second experiment assessed the direct effect of bacterial endotoxin on vascular reactivity.
- The third experiment investigated how arteries and veins in the palmar digital tissue reacted to the introduction of angiotensin II, norepinephrine, prostaglandin F2 alpha, serotonin, and a thromboxane-endoperoxide analog (U46619).
Results and comparisons
- This baseline data was then compared to results gathered from horses in the early stages of laminitis.
- For the laminitis study, researchers induced Obel grade-I laminitis in horses experimentally using a carbohydrate overload.
- Dose responses were recorded for each substance at varying concentrations between 10(-8)M and 10(-4)M.
- The effectiveness of a drug was determined by calculating the mean effective concentration needed to induce a 50% maximal contraction (EC50).
- No differences were found in the EC50 concentrations and maximal contractions between forelimb and hind limb arteries and veins for any substance tested.
- Lastly, incubation with endotoxin did not affect how arteries and veins reacted to angiotensin II, norepinephrine, and serotonin.
Cite This Article
APA
Baxter GM, Laskey RE, Tackett RL, Moore JN, Allen D.
(1989).
In vitro reactivity of digital arteries and veins to vasoconstrictive mediators in healthy horses and in horses with early laminitis.
Am J Vet Res, 50(4), 508-517.
Publication
Researcher Affiliations
- Department of Large Animal Medicine, College of Veterinary Medicine, University of Georgia, Athens 30602.
MeSH Terms
- Angiotensin II / pharmacology
- Animals
- Arteries / physiology
- Endotoxins / pharmacology
- Extremities / blood supply
- Foot Diseases / physiopathology
- Foot Diseases / veterinary
- Forelimb / blood supply
- Hindlimb / blood supply
- Hoof and Claw
- Horse Diseases / physiopathology
- Horses
- Norepinephrine / pharmacology
- Prostaglandin Endoperoxides, Synthetic / pharmacology
- Serotonin / pharmacology
- Vasoconstriction / drug effects
- Vasoconstrictor Agents / pharmacology
- Veins / physiology
Citations
This article has been cited 6 times.- Klotz JL, McDowell KJ. Tall fescue ergot alkaloids are vasoactive in equine vasculature. J Anim Sci 2017 Nov;95(11):5151-5160.
- Menzies-Gow NJ, Wray H, Bailey SR, Harris PA, Elliott J. The effect of tumour necrosis factor-α and insulin on equine digital blood vessel function in vitro. Inflamm Res 2014 Aug;63(8):637-47.
- Leise BS, Watts MR, Roy S, Yilmaz AS, Alder H, Belknap JK. Use of laser capture microdissection for the assessment of equine lamellar basal epithelial cell signalling in the early stages of laminitis. Equine Vet J 2015 Jul;47(4):478-88.
- Stokes AM, Venugopal CS, Hosgood G, Eades SC, Moore RM. Comparison of 2 endothelin-receptor antagonists on in vitro responses of equine palmar digital arterial and venous rings to endothelin-1. Can J Vet Res 2006 Jul;70(3):197-205.
- Bailey SR, Baillon ML, Rycroft AN, Harris PA, Elliott J. Identification of equine cecal bacteria producing amines in an in vitro model of carbohydrate overload. Appl Environ Microbiol 2003 Apr;69(4):2087-93.
- Pawson P, Reid J, Nolan AM. The role of nitric oxide in the responses of the ovine digital artery to vasoactive agents and modification of these responses by endotoxin and cytokines. Br J Pharmacol 2000 May;130(1):109-17.
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