In vitro response of large colon arterial and venous rings to vasodilating drugs in horses.
Abstract: To determine in vitro vasomotor response of equine large colon arterial and venous rings with and without endothelium to vasodilator drugs, including dopamine (DOP), dopexamine (DPX), acepromazine (ACE), isoxsuprine (ISX), and nifedipine (NFP). Methods: 7 adult horses. Methods: Relaxation of large colon arteries and veins in response to vasodilating drugs was determined by measuring the change in tension of vessel rings when exposed to a cumulative concentration range (10(-8) to 10(-4)M) of each drug. Vessel rings, with and without endothelium, were mounted in organ baths, attached to a transducer, and contracted with norepinephrine (NE). Cumulative concentration-response relationships, percentage maximal relaxation, and EC50 (concentration of drug required to relax the NE-induced contracted tissue to 50% of its contracted state) values were calculated. Results: There were significant differences among drugs for EC50 (ACE = ISX NFP = DPX > DOP) values in veins. Endothelium removal from veins had no significant effect. There were no differences in EC50 values for arteries; however, percentage maximal relaxation was significantly different among drugs (ACE = ISX = NFP > DPX = DOP). Endothelial removal resulted in higher EC50 and lower percentage maximal relaxation values, compared with endothelium-intact arteries. Conclusions: ACE and ISX were the most potent and efficacious drugs evaluated and could potentially be used to improve blood flow after correction of large-colon volvulus. Dopamine cannot be recommended because of its biphasic response and potential to further decrease blood flow. Endothelium removal altered the vasodilatory responses of colonic arterial rings, but did not affect venous rings.
Publication Date: 1999-02-27 PubMed ID: 10048553
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- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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This research investigated how arteries and veins in the large colons of horses respond to different vasodilating drugs, with and without endothelium, a layer lining blood vessels. It found that acepromazine and isoxsuprine were most effective, potentially improving blood flow after colon twisting events. However, dopamine was deemed unsuitable due to its confusing response and risk of reducing blood flow further.
Methodology
- Seven adult horses provided artery and vein rings from their large colons for this experiment, some with the endothelium intact, and others without.
- These samples were mounted in organ baths and attached to a transducer, before being contracted using norepinephrine (NE).
- The study used various drugs known for vasodilation: dopamine (DOP), dopexamine (DPX), acepromazine (ACE), isoxsuprine (ISX), and nifedipine (NFP), to see how the vessels responded. The vessels’ relaxation in reaction to the drugs was measured by monitoring the change in tension of each ring.
- They used varying concentration levels of each drug (ranging from 10(-8) to 10(-4)M) to gain a cumulative concentration-response relationship for each.
- They calculated the concentration of each drug needed to relax the NE-induced contracted tissue to 50% of its contracted state, known as the EC50 value, and the percentage maximal relaxation was measured.
Results
- The results showed significant differences among the drugs in both their EC50 values and their maximum possible relaxation. Dopamine had a unique biphasic response, meaning it first increased and then decreased, potentially posing a risk of reducing blood flow further.
- When the endothelium was removed from the veins, there were no significant changes noticed. However, the EC50 values increased and the maximum relaxation percentage decreased quite significantly in the removed-endothelium arteries compared to those left intact.
Conclusions
- The study concluded that ACE and ISX were the most potent and efficacious drugs evaluated, suggesting that they could potentially be used to improve blood flow after the correction of large-colon volvulus, a condition in which the colon twists around itself.
- They advised against the use of dopamine due to its confounding response and the potential for further reducing blood flow.
- Finally, they noted that the removal of endothelium altered the vasodilatory responses of colonic arterial rings, but not the venous rings, suggesting different reactions across different areas of the body’s vasculature.
Cite This Article
APA
Sedrish SA, Venugopalan CS, Holmes EP, Koch CE, Moore RM.
(1999).
In vitro response of large colon arterial and venous rings to vasodilating drugs in horses.
Am J Vet Res, 60(2), 204-210.
Publication
Researcher Affiliations
- Department of Veterinary Clinical Sciences, School of Veterinary Medicine, Louisiana State University, Baton Rouge 70803, USA.
MeSH Terms
- Acepromazine / pharmacology
- Acepromazine / therapeutic use
- Animals
- Arteries / drug effects
- Cardiotonic Agents / pharmacology
- Cardiotonic Agents / therapeutic use
- Colon / blood supply
- Colon / drug effects
- Colon / physiopathology
- Colonic Diseases / physiopathology
- Colonic Diseases / therapy
- Colonic Diseases / veterinary
- Dopamine / analogs & derivatives
- Dopamine / pharmacology
- Dopamine / therapeutic use
- Dopamine Antagonists / pharmacology
- Dopamine Antagonists / therapeutic use
- Dose-Response Relationship, Drug
- Endothelium, Vascular / cytology
- Endothelium, Vascular / drug effects
- Endothelium, Vascular / physiology
- Horse Diseases / therapy
- Horses
- In Vitro Techniques
- Intestinal Obstruction / physiopathology
- Intestinal Obstruction / therapy
- Intestinal Obstruction / veterinary
- Isoxsuprine / pharmacology
- Isoxsuprine / therapeutic use
- Muscle Contraction / drug effects
- Muscle, Smooth, Vascular / cytology
- Muscle, Smooth, Vascular / drug effects
- Nifedipine / pharmacology
- Nifedipine / therapeutic use
- Norepinephrine / pharmacology
- Vasodilator Agents / pharmacology
- Vasodilator Agents / therapeutic use
- Veins / drug effects
Citations
This article has been cited 1 times.- Simpson J. Recent advances in diverticular disease. Curr Gastroenterol Rep 2004 Oct;6(5):417-22.
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