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Equine veterinary journal2010; 41(8); 772-777; doi: 10.2746/042516409x421624

Plasma concentrations, behavioural and physiological effects following intravenous and intramuscular detomidine in horses.

Abstract: Detomidine hydrochloride is used to provide sedation, muscle relaxation and analgesia in horses, but a lack of information pertaining to plasma concentration has limited the ability to correlate drug concentration with effect. Objective: To build on previous information and assess detomidine for i.v. and i.m. use in horses by simultaneously assessing plasma drug concentrations, physiological parameters and behavioural characteristics. Objective: Systemic effects would be seen following i.m. and i.v. detomidine administration and these effects would be positively correlated with plasma drug concentrations. Methods: Behavioural (e.g. head position) and physiological (e.g. heart rate) responses were recorded at fixed time points from 4 min to 24 h after i.m. or i.v. detomidine (30 microg/kg bwt) administration to 8 horses. Route of administration was assigned using a balanced crossover design. Blood was sampled at predetermined time points from 0.5 min to 48 h post administration for subsequent detomidine concentration measurements using liquid chromatography-mass spectrometry. Data were summarised as mean +/- s.d. for subsequent analysis of variance for repeated measures. Results: Plasma detomidine concentration peaked earlier (1.5 min vs. 1.5 h) and was significantly higher (105.4 +/- 71.6 ng/ml vs. 6.9 +/- 1.4 ng/ml) after i.v. vs. i.m. administration. Physiological and behavioural changes were of a greater magnitude and observed at earlier time points for i.v. vs. i.m. groups. For example, head position decreased from an average of 116 cm in both groups to a low value 35 +/- 23 cm from the ground 10 min following i.v. detomidine and to 64 +/- 24 cm 60 min after i.m. detomidine. Changes in heart rate followed a similar pattern; low value of 17 beats/min 10 min after i.v. administration and 29 beats/min 30 min after i.m. administration. Conclusions: Plasma drug concentration and measured effects were correlated positively and varied with route of administration following a single dose of detomidine. Conclusions: Results support a significant influence of route of administration on desirable and undesirable drug effects that influence case management.
Publication Date: 2010-01-26 PubMed ID: 20095225DOI: 10.2746/042516409x421624Google Scholar: Lookup
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  • Clinical Trial
  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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This research focuses on the relationship between plasma concentrations of the drug detomidine hydrochloride in horses and its physiological and behavioural effects when administered either intravenously (i.v.) or intramuscularly (i.m.). The study found that effects were positively influenced by the plasma drug concentration, which varied based on the administration route, therefore impacting the drug’s desired and undesirable effects.

Methods and Objectives

  • The study aimed to expand existing research on detomidine, a drug used to sedate horses, by assessing its effects when administered through i.v. and i.m. routes. In so doing, the researchers aimed to build a correlation between plasma drug concentrations and their systemic effects.
  • The researchers studied the behavioural (like head position) and physiological (like heart rate) responses of 8 horses after the administration of detomidine. The study followed a balanced crossover design; thus, each horse experienced both i.v. and i.m. administration at different times.
  • Blood samples at predetermined intervals (from 0.5 min to 48 h post-administration) were collected for subsequent detomidine concentration measurements using liquid chromatography-mass spectrometry.

Results

  • The plasma concentration of detomidine peaked earlier and was significantly higher with i.v. administration compared to i.m. administration.
  • The physiological and behavioural changes were more significant and observed at earlier time points for the i.v. group compared to the i.m. group. For instance, the average head position across both groups dropped to about 35 cm from the ground 10 min after i.v. administration, while it decreased to about 64 cm after 60 min of i.m. administration.
  • The heart rate showed a similar pattern, with a lower value of 17 beats/min 10 min following i.v. administration, and 29 beats/min 30 min after i.m. administration.

Conclusions

  • The results showed a positive correlation between the detomidine plasma concentration and the effects measured, which varied based on the route of administration. This finding is critical because the plasma concentration affects the desirable and undesirable effects of the drug, thereby impacting case management.

Cite This Article

APA
Mama KR, Grimsrud K, Snell T, Stanley S. (2010). Plasma concentrations, behavioural and physiological effects following intravenous and intramuscular detomidine in horses. Equine Vet J, 41(8), 772-777. https://doi.org/10.2746/042516409x421624

Publication

ISSN: 0425-1644
NlmUniqueID: 0173320
Country: United States
Language: English
Volume: 41
Issue: 8
Pages: 772-777

Researcher Affiliations

Mama, K R
  • Department of Clinical Sciences, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Fort Collins, Colorado 80523, USA.
Grimsrud, K
    Snell, T
      Stanley, S

        MeSH Terms

        • Animals
        • Cross-Over Studies
        • Dose-Response Relationship, Drug
        • Female
        • Heart Rate / drug effects
        • Horses
        • Hypnotics and Sedatives / administration & dosage
        • Hypnotics and Sedatives / blood
        • Hypnotics and Sedatives / pharmacokinetics
        • Hypnotics and Sedatives / pharmacology
        • Imidazoles / administration & dosage
        • Imidazoles / blood
        • Imidazoles / pharmacokinetics
        • Imidazoles / pharmacology
        • Injections, Intramuscular
        • Injections, Intravenous
        • Male
        • Pain / prevention & control
        • Pain Measurement / veterinary
        • Respiration / drug effects
        • Time Factors

        Citations

        This article has been cited 6 times.
        1. de Oliveira AR, Gozalo-Marcilla M, Ringer SK, Schauvliege S, Fonseca MW, Esteves Trindade PH, Prospero Puoli Filho JN, Luna SPL. Development and validation of the facial scale (FaceSed) to evaluate sedation in horses.. PLoS One 2021;16(6):e0251909.
          doi: 10.1371/journal.pone.0251909pubmed: 34061878google scholar: lookup
        2. Stover BC, Caulkett NA. Anesthesia techniques used for field castration of 10 intractable horses.. Can Vet J 2021 May;62(5):501-504.
          pubmed: 33967290
        3. de Oliveira AR, Gozalo-Marcilla M, Ringer SK, Schauvliege S, Fonseca MW, Trindade PHE, Puoli Filho JNP, Luna SPL. Development, Validation, and Reliability of a Sedation Scale in Horses (EquiSed).. Front Vet Sci 2021;8:611729.
          doi: 10.3389/fvets.2021.611729pubmed: 33665216google scholar: lookup
        4. Tapio H, Raekallio MR, Mykkänen A, Männikkö S, Scheinin M, Bennett RC, Vainio O. Effects of vatinoxan on cardiorespiratory function and gastrointestinal motility during constant-rate medetomidine infusion in standing horses.. Equine Vet J 2019 Sep;51(5):646-652.
          doi: 10.1111/evj.13085pubmed: 30793362google scholar: lookup
        5. Fielding CL. Practical Fluid Therapy and Treatment Modalities for Field Conditions for Horses and Foals with Gastrointestinal Problems.. Vet Clin North Am Equine Pract 2018 Apr;34(1):155-168.
          doi: 10.1016/j.cveq.2017.11.013pubmed: 29534809google scholar: lookup
        6. Grimsrud KN, Ait-Oudhia S, Durbin-Johnson BP, Rocke DM, Mama KR, Rezende ML, Stanley SD, Jusko WJ. Pharmacokinetic and pharmacodynamic analysis comparing diverse effects of detomidine, medetomidine, and dexmedetomidine in the horse: a population analysis.. J Vet Pharmacol Ther 2015 Feb;38(1):24-34.
          doi: 10.1111/jvp.12139pubmed: 25073816google scholar: lookup