Actions of non-steroidal anti-inflammatory drugs on equine leucocyte movement in vitro.
Abstract: The direct effects of four non-steroidal anti-inflammatory drugs (NSAIDs) on equine polymorphonuclear (PMN) and mononuclear (MN) leucocyte movement were investigated using two in vitro assay systems. The Boyden chamber microfilter technique measures both chemokinetic and chemotactic locomotion, and the agarose microdroplet assay measures solely chemokinesis. Zymosan-activated plasma (ZAP) and the synthetic peptide N-formyl-methionyl-leucyl-phenylalanine (FMLP) were used as standard chemoattractants for PMN and MN leucocytes, respectively. The actions of six concentrations of each NSAID, indomethacin (50 microM-10 mM), phenylbutazone (10 microM-1 mM), oxyphenbutazone (2.5 microM-500 microM) and flunixin (0.1 microM-50 microM), in suppressing cell movement induced by ZAP and FMLP were investigated. All four drugs exerted inhibitory effects on induced movement of both cell types in the Boyden chamber assay, usually in a concentration-dependent manner, although oxyphenbutazone action on PMN cells occurred only at the highest concentration tested. Significant inhibition of PMN and MN cell locomotion was produced by indomethacin, flunixin and oxyphenbutazone, and inhibition of PMN movement by phenylbutazone occurred in the agarose microdroplet assay. Flunixin was the most potent of the four drugs investigated in both assay systems. The findings may be of importance to the use of phenylbutazone and flunixin as NSAIDs in equine medicine, since the concentrations used were similar to concentrations of both drugs and the phenylbutazone metabolite oxyphenbutazone previously reported to occur in equine plasma and inflammatory exudate.
Publication Date: 1987-06-01 PubMed ID: 3612943DOI: 10.1111/j.1365-2885.1987.tb00092.xGoogle Scholar: Lookup
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- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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The research investigated the effects of four different non-steroidal anti-inflammatory drugs (NSAIDs) on the movement of equine leukocytes (white blood cells), using two different in vitro (outside a living organism) tests. The results showed that all four drugs can inhibit the movement of these cells in concentration-dependent manners, which could have implications for their use in equine medicine.
Research Methodology
- The researchers employed two different in vitro assays. The first one, called the Boyden chamber microfilter technique, is used to measure both chemokinetic (random cell movement) and chemotactic (movement directed by certain chemicals) locomotion. The second one, the agarose microdroplet assay, measures only chemokinesis.
- Two chemoattractants—zymosan-activated plasma (ZAP) and N-formyl-methionyl-leucyl-phenylalanine (FMLP)—were used. ZAP is used to attract polymorphonuclear (PMN) leucocytes, a type of white blood cell most commonly consisting of neutrophils, while FMLP is used to attract mononuclear (MN) leucocytes, which include lymphocytes and monocytes.
- The study examined the effects of six concentrations of each NSAID. The NSAIDs tested were indomethacin, phenylbutazone, oxyphenbutazone (a metabolite of phenylbutazone), and flunixin.
Results
- All four NSAIDs showed inhibitory effects on induced movement of both PMN and MN leucocytes in the Boyden chamber assay. This means they prevent or limit the movement of these cells when attracted by the chemoattractants.
- Oxyphenbutazone affected PMN cells only at the highest concentration tested, exhibiting a less potent effect compared to the other NSAIDs.
- In the agarose microdroplet assay, indomethacin, flunixin, and oxyphenbutazone inhibited both PMN and MN cell locomotion. Additionally, phenylbutazone suppressed the movement of PMN cells.
- Among the NSAIDs studied, flunixin was found to have the most potent effect in both assay systems.
Implications and Conclusions
- The findings may be significant for the usage of these NSAIDs in equine medicine. Both phenylbutazone and flunixin are commonly used in the treatment of equine pain and inflammation, and their effects on leukocyte movement can influence their therapeutic effectiveness.
- As the concentration levels used in the study are similar to those found in equine plasma and inflammatory exudates, the results could influence the dosage and application of these drugs in a real-world veterinary context.
Cite This Article
APA
Dawson J, Lees P, Sedgwick AD.
(1987).
Actions of non-steroidal anti-inflammatory drugs on equine leucocyte movement in vitro.
J Vet Pharmacol Ther, 10(2), 150-159.
https://doi.org/10.1111/j.1365-2885.1987.tb00092.x Publication
Researcher Affiliations
MeSH Terms
- Animals
- Anti-Inflammatory Agents, Non-Steroidal / pharmacology
- Cell Movement / drug effects
- Chemotaxis, Leukocyte / drug effects
- Clonixin / analogs & derivatives
- Clonixin / pharmacology
- Horses / blood
- Indomethacin / pharmacology
- Leukocytes / drug effects
- Leukocytes / physiology
- Monocytes / drug effects
- Monocytes / physiology
- Neutrophils / drug effects
- Neutrophils / physiology
- Oxyphenbutazone / pharmacology
- Phenylbutazone / pharmacology
Citations
This article has been cited 2 times.- Kankaanranta H, Moilanen E, Vapaatalo H. Comparison of in vitro effects of flunixin and tolfenamic acid on human leukocyte and platelet functions. Inflammation 1993 Aug;17(4):417-25.
- King JN. The use of intradermal carrageenan in calves to estimate the dose of oxindanac, a nonsteroidal anti-inflammatory drug. Can J Vet Res 1993 Oct;57(4):215-22.
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