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Pharmacokinetics of and serum thromboxane suppression by flunixin meglumine in healthy foals during the first month of life.

Abstract: Age and species reportedly affect the pharmacokinetic variables of nonsteroidal anti-inflammatory drugs. We determined the effect of age on flunixin pharmacokinetic variables in foals during the first month of life. We also estimated the physiologic activity of the drug in neonatal foals by determining the effect of flunixin on thromboxane production during clotting of blood taken from the foals. Flunixin disposition and clearance were determined after IV administration of 1.1 mg of drug/kg of body weight to 5 healthy foals when they were 24 to 28 hours, 10 to 11 days, and 27 to 28 days old. The area under the curve (2,471 micrograms.min/ml), mean residence time (477 minutes), and zero-time intercept of the elimination phase (4,853 ng/ml) were significantly (P = 0.05) greater, the elimination half-life (339 minutes) and slope of the elimination phase (0.002 L/min) were significantly (P = 0.05) longer, and total body clearance (0.482 ml/min/kg) and zero-time intercept for the distribution phase (2,092 ng/ml) were significantly (P = 0.05) lower at 24 to 28 hours. At each age, a biexponential equation was best fitted to the plasma flunixin concentration from each foal. Thromboxane B2 production during clotting of blood was significantly (P = 0.05) suppressed for 12 hours after flunixin meglumine administration at all ages. Therefore, it appears that although age does alter the disposition and elimination of flunixin in neonatal foals, this effect may be of little consequence because the drug's physiologic activity in foals appears similar to that in mature horses.
Publication Date: 1993-12-01 PubMed ID: 8116942
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research examined how the age of foals in the first month of life impacts the pharmacokinetic variables of flunixin, a nonsteroidal anti-inflammatory drug. The study also estimated the drug’s physiologic activity in the neonatal foals by observing flunixin’s effect on blood clotting.

Pharmacokinetics of Flunixin in Foals

  • The researchers administered an intravenous dose of flunixin to five healthy foals at three different ages: 24-28 hours, 10-11 days, and 27-28 days. The variables studied included the area under the curve, mean residence time, zero-time intercept of the elimination phase, and several others.
  • The results showed significant differences in these variables based on the age of the foals. For instance, the area under the curve, mean residence time, and zero-time intercept of the elimination phase were higher in foals aged 24-28 hours than in the older foals.
  • Conversely, the elimination half-life and slope of the elimination phase were longer, while the total body clearance and zero-time intercept for the distribution phase were lower at the same age. The researchers used a biexponential equation for the best fit of plasma flunixin concentration for each foal at different ages.

Physiologic Activity of Flunixin in Foals

  • Additionally, the study measured thromboxane B2 production, a process affected by flunixin, during the clotting of blood from the foals. This measure indicates the physiologic activity of the drug in neonatal foals.
  • This production was significantly suppressed for 12 hours after flunixin administration at all ages. The authors concluded that even though the age of foals alters the disposition and elimination of flunixin, this may not have significant repercussions since the drug’s physiologic action on foals appears to be similar to its effect on mature horses.

In conclusion, while the study confirms that age affects the pharmacokinetics of flunixin in foals, this has little observable impact on the drug’s physiologic action during the first month of a foal’s life.

Cite This Article

APA
Semrad SD, Sams RA, Ashcraft SM. (1993). Pharmacokinetics of and serum thromboxane suppression by flunixin meglumine in healthy foals during the first month of life. Am J Vet Res, 54(12), 2083-2087.

Publication

ISSN: 0002-9645
NlmUniqueID: 0375011
Country: United States
Language: English
Volume: 54
Issue: 12
Pages: 2083-2087

Researcher Affiliations

Semrad, S D
  • Department of Medical Sciences, University of Wisconsin, Madison 53706.
Sams, R A
    Ashcraft, S M

      MeSH Terms

      • Aging / blood
      • Analysis of Variance
      • Animals
      • Animals, Newborn
      • Anti-Inflammatory Agents, Non-Steroidal / pharmacokinetics
      • Anti-Inflammatory Agents, Non-Steroidal / pharmacology
      • Blood Coagulation / drug effects
      • Blood Specimen Collection / methods
      • Blood Specimen Collection / veterinary
      • Clonixin / analogs & derivatives
      • Clonixin / blood
      • Clonixin / pharmacokinetics
      • Clonixin / pharmacology
      • Female
      • Horses
      • Male
      • Metabolic Clearance Rate
      • Thromboxane B2 / blood

      Citations

      This article has been cited 4 times.
      1. Fadel C, Giorgi M. Synopsis of the pharmacokinetics, pharmacodynamics, applications, and safety of firocoxib in horses. Vet Anim Sci 2023 Mar;19:100286.
        doi: 10.1016/j.vas.2023.100286pubmed: 36684818google scholar: lookup
      2. Flood J, Stewart AJ. Non-Steroidal Anti-Inflammatory Drugs and Associated Toxicities in Horses. Animals (Basel) 2022 Oct 26;12(21).
        doi: 10.3390/ani12212939pubmed: 36359062google scholar: lookup
      3. Mallicote M, House AM, Sanchez LC. A review of foal diarrhoea from birth to weaning. Equine Vet Educ 2012 Apr;24(4):206-214.
      4. Pearson JM, Pajor E, Campbell J, Levy M, Caulkett N, Windeyer MC. A randomised controlled trial investigating the effects of administering a non-steroidal anti-inflammatory drug to beef calves assisted at birth and risk factors associated with passive immunity, health, and growth. Vet Rec Open 2019;6(1):e000364.
        doi: 10.1136/vetreco-2019-000364pubmed: 31673377google scholar: lookup