Narcotic analgesics, their detection and pain measurement in the horse: a review.
Abstract: Narcotic analgesics produce pharmacological effects by interacting with specific opiate receptors. At least five major types of opiate receptors have been recognised. These include mu (morphine) and kappa (ethylketazocine) receptor types. Narcotic analgesics which interact with mu receptors produce locomotor and autonomic stimulation at doses that produce little or no analgesia. Therefore, use of these drugs as analgesics in equine medicine has not been very satisfactory. Theoretical considerations suggested that the role of kappa agonists in equine analgesia be investigated. Using a pure kappa agonist, U-50, 488H, good analgesia was produced in the horse with little or no locomotor stimulation or autonomic effects. These data suggest that kappa agonists may be superior analgesics for clinical use in the horse. On the other hand, the locomotor stimulant effects of mu agonist analgesics enable their use as illegal medications. Specifically, these agents produce a good running response, signs of central nervous stimulation and analgesia, all potentially useful effects in a racehorse. Regulatory control of most narcotic analgesics can be obtained by high performance thin layer chromatographic screening. However, effective screening for the fentanyls and small doses of etorphine can only be achieved by use of immunoassay.
Publication Date: 1989-01-01 PubMed ID: 2563969DOI: 10.1111/j.2042-3306.1989.tb02081.xGoogle Scholar: Lookup
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- Journal Article
- Research Support
- Non-U.S. Gov't
- Review
Summary
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The research focuses on the effectiveness of narcotic analgesics (pain relievers) used in equine medicine and their side effects, with particular emphasis on those interacting with mu and kappa opioid receptors.
Narcotic Analgesics and Opiate Receptors
- This study scrutinizes the relationship between narcotic analgesics and opiate receptors. It highlights morphine and ethylketazocine specifically, which interact with mu and kappa receptors respectively.
- Opiate receptors in mammals are proteins that respond to opioids (naturally occurring substances found in opium poppy plants which include morphine and codeine), synthesizing their desired effect.
- At least five types of opiate receptors have been identified, but this study focuses mainly on mu and kappa receptor types.
Effects of Mu and Kappa Agonist Analgesics
- The study reveals that narcotic analgesics interacting with mu receptors produce locomotor and autonomic stimulation, effects that facilitate movement or control body functions, but, importantly, they may not relieve pain effectively. This makes these drugs inadequate for use as pain-killers in equine medicine.
- The research also explores the use of kappa agonists, which appear to be more satisfactory for equine pain relief. Using a pure kappa agonist, U-50, 488H, resulted in effective analgesia (pain relief) with little or no locomotor or autonomic side effects. This suggests that kappa agonists might be better pain relievers for clinical use in horses.
- The study also mentions the controversial use of mu agonist analgesics in racehorses. While these drugs can potentially produce positive effects, like an enhanced running response and central nervous system stimulation, their usage is considered illegal due to these performance-enhancing qualities.
Detection and Regulation of Narcotic Analgesics
- The paper delves into the detection and regulation of narcotic analgesics, acknowledging that most can be identified via high-performance thin-layer chromatographic screening.
- However, for specific drugs like the fentanyls and small doses of etorphine, effective screening requires the use of immunoassay, a biochemistry test that measures the presence or concentration of molecules.
Cite This Article
APA
Kamerling S, Wood T, DeQuick D, Weckman TJ, Tai C, Blake JW, Tobin T.
(1989).
Narcotic analgesics, their detection and pain measurement in the horse: a review.
Equine Vet J, 21(1), 4-12.
https://doi.org/10.1111/j.2042-3306.1989.tb02081.x Publication
Researcher Affiliations
- Department of Veterinary Physiology, College of Veterinary Medicine, Louisiana State University, Baton Rouge.
MeSH Terms
- 3,4-Dichloro-N-methyl-N-(2-(1-pyrrolidinyl)-cyclohexyl)-benzeneacetamide, (trans)-Isomer
- Analgesics, Opioid / analysis
- Analgesics, Opioid / metabolism
- Analgesics, Opioid / pharmacokinetics
- Analgesics, Opioid / pharmacology
- Animals
- Butorphanol / pharmacology
- Chromatography, Thin Layer
- Cyclazocine / analogs & derivatives
- Cyclazocine / pharmacology
- Ethylketocyclazocine
- Etorphine / analysis
- Etorphine / pharmacology
- Fentanyl / analysis
- Fentanyl / pharmacology
- Horses / metabolism
- Horses / physiology
- Morphine / pharmacokinetics
- Morphine / pharmacology
- Pain Measurement / veterinary
- Pentazocine / pharmacokinetics
- Pentazocine / pharmacology
- Pyrrolidines / pharmacology
- Radioimmunoassay
- Receptors, Opioid / metabolism
Citations
This article has been cited 3 times.- Machado Filho LC, Hurnik JF, Ewing KK. A thermal threshold assay to measure the nociceptive response to morphine sulphate in cattle. Can J Vet Res 1998 Jul;62(3):218-23.
- Mama KR, Pascoe PJ, Steffey EP. Evaluation of the interaction of mu and kappa opioid agonists on locomotor behavior in the horse. Can J Vet Res 1993 Apr;57(2):106-9.
- Guzmán JFC, Gontijo AS, Melgaço ES, Faria SA, Baldi MLC, Sousa LN, Wenceslau RR, Fantini P, Xavier ABDS, Beier SL. Analgesic and Gastrointestinal Effects of Morphine in Equines. Animals (Basel) 2025 Feb 17;15(4).
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