Characterization of vasodilatory adenosine receptors in equine digital veins.
Abstract: Isolated equine digital veins (EDVs) which had been denuded of their endothelium were used to study adenosine receptors causing vasodilation. When the blood vessel wall tension was raised with the thromboxanemimetic, U44069 (30 nM), the order of vasodilator potency of adenosine receptor agonists was: 5'-N-ethylcarboxamidoadenosine (NECA) > 2-p-(2-carboxyethyl)phenyl amino-5'-N-ethylcarboxamido-adenosine (CGS 21680) > 5'-N-methylcarboxamido-adenosine (MECA) > N6-cyclohexyladenosine (CHA) > N6-cyclopentyladenosine (CPA) > N6-2-(4-Aminophenyl)ethyladenosine (APNEA) > adenosine. Removal of the endothelium had no significant effect on the responses to NECA. The adenosine receptor antagonists, 8-cyclopentyl-1,3-dipropylxanthine (DPCPX; A1-selective) and xanthine amine cogener (XAC; non-selective antagonist) inhibited responses to NECA and CHA in a competitive manner and XAC proved to be 8-25 times more potent than DPCPX against both agonists. These data support the presence of A2 adenosine receptors in EDVs, located on the vascular smooth muscle cells, which are most likely to be of the A2A-adenosine receptor subtype. A direct comparison between the potency and efficacy of NECA and adenosine as vasodilators of EDV and equine digital arteries was made and both agonists proved to be significantly more potent and efficacious as vasodilators of EDVs. These data suggest that adenosine may be an important local mediator regulating blood flow through the digital circulation and that its generation under hypoxic conditions would lead to selective venodilation.
Publication Date: 1998-03-21 PubMed ID: 9507461DOI: 10.1046/j.1365-2885.1998.00106.xGoogle Scholar: Lookup
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- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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The study explores the role of adenosine receptors in causing vasodilation in horse-specific digital veins. The research shows that adenosine may be a key local mediator that controls the blood flow through the digital circulation, particularly under hypoxic or low-oxygen-level conditions.
Methods and Materials
- The study used isolated equine digital veins (EDVs), which are specific veins found in horses, denuded of their endothelium, or interior lining.
- The veins were subjected to increased wall tension using the thromboxanemimetic of U44069 (a chemical compound).
- The veins were then exposed to different adenosine receptor agonists, following which the vasodilator potency of these agonists was assessed.
- Different adenosine receptor antagonists were also used to inhibit responses.
Results
- The relative vasodilator potency of the adenosine receptor agonists was determined in the following decreasing order: NECA, CGS 21680, MECA, CHA, CPA, APNEA, and Adenosine.
- The removal of the endothelium had no significant effect on the responses to NECA.
- XAC, a non-selective antagonist, was 8-25 times more potent than A1-selective antagonist DPCPX against both NECA and CHA.
- Data suggested the presence of A2 adenosine receptors in EDVs, located on the vascular smooth muscle cells, which are likely to be of the A2A-adenosine receptor subtype.
Comparison and Effectiveness
- A direct comparison of the potency and efficacy of NECA and adenosine as vasodilators of EDV and equine digital arteries was made.
- The results showed both NECA and adenosine to be significantly more potent and effective as vasodilators of EDVs.
Conclusion
- The research suggests that adenosine may act as an important local mediator, regulating blood flow through the digital circulation in horses.
- The generation of adenosine under hypoxic conditions, or conditions with low oxygen levels, would lead to selective venodilation, or the dilation of veins, which is a natural body response designed to increase blood flow and oxygen to various body parts.
Cite This Article
APA
Elliott J, Brady FE.
(1998).
Characterization of vasodilatory adenosine receptors in equine digital veins.
J Vet Pharmacol Ther, 21(1), 74-81.
https://doi.org/10.1046/j.1365-2885.1998.00106.x Publication
Researcher Affiliations
- Department of Veterinary Basic Sciences, Royal Veterinary College, London, UK.
MeSH Terms
- Adenosine / analogs & derivatives
- Adenosine / pharmacology
- Animals
- Endothelium, Vascular / physiology
- Horses
- In Vitro Techniques
- Isometric Contraction / drug effects
- Muscle, Smooth, Vascular / drug effects
- Muscle, Smooth, Vascular / physiology
- Purinergic P1 Receptor Agonists
- Purinergic P1 Receptor Antagonists
- Receptors, Purinergic P1 / physiology
- Structure-Activity Relationship
- Toes / blood supply
- Vasodilation / drug effects
- Vasodilation / physiology
- Veins / drug effects
- Veins / physiology
Citations
This article has been cited 2 times.- 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.
- Tilley SL, Wagoner VA, Salvatore CA, Jacobson MA, Koller BH. Adenosine and inosine increase cutaneous vasopermeability by activating A(3) receptors on mast cells.. J Clin Invest 2000 Feb;105(3):361-7.
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